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WHAT IS INVASIVE LOBULAR CARCINOMA?

Invasive lobular carcinoma (ILC) is a type of breast cancer that has spread beyond the lobules and ducts, potentially spreading to the lymph nodes and other parts of the body.

Lobular Breast Cancer

Lobular breast cancer is a subtype of breast cancer that originates in the lobules, the glands that produce milk in the breast tissue. This differs from the more common ductal carcinoma, which starts in the milk ducts. It is classified as invasive when cancer cells spread beyond the lobules into surrounding breast tissue.

The exact causes of lobular breast cancer remain unclear, but several risk factors have been identified. These include genetic mutations (such as alterations in the CDH1 gene), hormonal factors (such as increased estrogen levels), and a family history of breast cancer. One of the challenges with lobular breast cancer is that it often does not present with a distinct lump, making early detection through mammograms or breast self-examination difficult.

Early diagnosis is crucial for effective treatment and improved outcomes. Treatment options typically include a combination of surgery, radiation therapy, chemotherapy, endocrine (or hormone) therapy, and/or targeted therapies, depending on the stage and characteristics of the cancer. Ongoing advances in research continue to enhance understanding and treatment options for lobular breast cancer, offering hope for improved outcomes and quality of life for those affected.

What are the Symptoms of Invasive Lobular Carcinoma?

Some patients diagnosed with ILC may not present with any symptoms. When symptoms are present, they may include:

  • A new lump in the breast, armpit area or around the collarbone.
  • Thickening or hardening in the breast.
  • A change in breast size or shape.
  • Changes to the nipple, such as sores or crusting, an ulcer or inverted nipple.
  • Clear or bloody nipple discharge.
  • Changes to the skin including redness, puckering or dimpling (an ‘orange peel’ appearance).
  • Breast tenderness or pain.

How is Lobular Breast Cancer Diagnosed?

Diagnosing ILC can be challenging due to the way the cells grow through the breast tissue. ILC typically grows in a line rather than a mass, making it difficult to see the full extent of the disease on a mammogram. Additional imaging with an ultrasound and breast MRI is sometimes required.

Imaging Tests

  • Mammogram: A specialised X-ray of the breast to detect any abnormalities or unusual growths. However, ILC can be difficult to identify on mammograms.
  • Ultrasound: This technique uses sound waves create images, providing a clearer view, especially if the mammogram raises suspicions.
  • Breast MRI: A more detailed imaging test that can provide a comprehensive picture of the breast tissue.

Biopsy

If an imaging test shows an abnormality, a biopsy is performed. This involves taking a small sample of tissue from the suspicious area. A core needle biopsy is commonly used, where a thin, hollow needle is used to collect tissue for examination.

Pathology Examination

The collected tissue is sent to a laboratory, where a pathologist examines it under a microscope. The pathologist looks for specific characteristics, such as the presence of invasive lobular structures.

Hormone Receptor Testing

Testing for oestrogen and progesterone receptors helps determine if the cancer cells are sensitive to endocrine (or hormone) therapies.

Lymph Node Examination

If cancer is confirmed, the doctor may examine nearby lymph nodes to see if the cancer has spread. This is an important step in determining the extent or stage of the cancer.

Staging

Understanding the stage of cancer is crucial for planning the most appropriate treatment. Staging considers the size of the tumour, whether it has spread to the lymph nodes, and whether it has spread to other parts of the body.

Stages of Lobular Carcinoma

Invasive lobular carcinoma (ILC) goes through different stages. It is crucial for doctors to know the stage of the cancer to assess the severity of the disease and guide the treatment plan. The stages of cancer are:

  • Stage 0 (Carcinoma in Situ): At this early stage, cancerous cells are confined to the lobules, and there is no invasion into surrounding tissues. This is often referred to as carcinoma in situ, meaning the cancer is localised and has not spread.
  • Stage I: Cancer is still relatively localised, typically confined to the breast tissue. The tumour size is relatively small, and there is no evidence of lymph node involvement.
  • Stage II: The tumour is larger or may involve nearby lymph nodes. Despite the larger tumour size, the cancer is still predominantly within the breast.
  • Stage III: Cancer has spread more extensively to surrounding tissues and lymph nodes. The tumour may be large, and there may be evidence of invasion into nearby structures.
  • Stage IV (Metastatic): At this advanced stage, cancer has spread beyond the breast and nearby lymph nodes to other organs or distant parts of the body. This is considered advanced and challenging to treat.

How is Invasive Lobular Carcinoma (ILC) Treated?

ILC are typically oestrogen receptor positive breast cancers, which makes them sensitive to the endocrine (or hormone blocking) treatments such as tamoxifen.

Depending on the stage of ILC, treatment may include a combination of surgery, radiation therapy, chemotherapy, endocrine (hormone) therapy, and targeted therapies. Treatment for ILC also may include breast surgery, radiation therapy and chemotherapy. In most cases, ILC is usually more responsive to endocrine therapy than chemotherapy and is generally preferred.

What are my Chances of Survival (Prognosis) if I am Diagnosed with Invasive Lobular Carcinoma?

Typically, invasive lobular carcinoma tumours are associated with a good prognosis, as they tend to be low grade and oestrogen receptor positive. However, this will depend on your age, health status, tumour type and stage of cancer.

Your age, stage of disease and tumour type has the greatest impact on your chance of surviving five years past your breast cancer diagnosis. For stage 1 breast cancer, the chance of surviving 5 years or beyond is nearly 100%. However, for stage 4 breast cancer, the chance of surviving 5 years or beyond drops to 22%.

Overall, the five-year survival rate for women diagnosed with breast cancer is 91.5%, and 86.4% for men.

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WHAT IS INVASIVE DUCTAL CARCINOMA?

Invasive ductal carcinoma (IDC) is a broad term used to classify cancer that began growing in a milk duct and has invaded the fibrous or fatty tissue of the breast outside the duct.

Invasive ductal carcinoma (IDC) is a type of breast cancer that originates in a milk duct and invades the surrounding fibrous or fatty tissue of the breast. From there, it has the potential to spread to other organs in the body.

How Common is Invasive Ductal Carcinoma?

Invasive ductal carcinoma accounts for around 80 percent of all breast cancer diagnoses. It is also the most common type of breast cancer that affects men.

What are the Symptoms of Invasive Ductal Carcinoma?

Some patients diagnosed with IDC may not present with any symptoms. When symptoms are present, they may include:

  • A new lump in the breast, or armpit area
  • A change in breast size or shape
  • Changes to the nipple, such as sores or crusting, an ulcer or inverted nipple
  • Clear or bloody nipple discharge
  • Changes to the skin including redness, puckering, or dimpling (an ‘orange peel’ appearance)
  • Breast tenderness or pain

How is Invasive Ductal Carcinoma Diagnosed?

Invasive ductal carcinoma is diagnosed through a combination of a physical exam, imaging tests like mammogram and ultrasound, and a biopsy where a small tissue sample is examined for cancer cells. This help doctors confirm the presence of cancer and plan the best treatment.

How is Invasive Ductal Carcinoma Treated?

The treatment of IDC depends on the stage of the cancer and the characteristics of the tumour, including its size, location, spread, and type. Treatment options may include a combination of radiation therapy, chemotherapy, hormone therapy, and/or surgery.

What are my chances of Survival (prognosis) if I am Diagnosed with Invasive Ductal Carcinoma?

In Australia and New Zealand, survival rates for invasive ductal carcinoma have improved thanks to advancements in clinical trials research, which have led to more tailored and advanced treatments, prevention strategies, and screening techniques.

However, for some people, their breast cancer will progress to an advanced or metastatic stage which greatly reduces their chances of survival.

Factors such as age, stage of disease, and tumour type can impact the likelihood of surviving five years past a breast cancer diagnosis.

Overall, the five-year survival rate for women diagnosed with breast cancer is 91.5%, and 86.4% for men.

FAQ’s

How Serious is Invasive Ductal Carcinoma?

Invasive ductal carcinoma is a serious form of breast cancer, as it has the potential to spread beyond the milk ducts where it originates. The seriousness of IDC largely depends on the grade of the cancer and the stage at which it is diagnosed.  Early detection and appropriate treatment are crucial for a better prognosis.

Is Invasive Breast Cancer Aggressive?

Yes, invasive breast cancer, including invasive ductal carcinoma, is considered aggressive because it can invade surrounding tissues and spread to other parts of the body. The level of aggressiveness can vary depending on the grade of the cancer, with invasive ductal carcinoma   grade 3 being more aggressive compared to grade 1.

What is the Difference Between DCIS and Invasive Ductal Carcinoma?

The key difference between DCIS (ductal carcinoma in situ) and invasive ductal carcinoma lies in their potential to spread. DCIS is a non-invasive cancer, meaning the cancer cells are confined within the ducts and have not invaded surrounding tissues. On the other hand, invasive ductal carcinoma breaks through the duct walls and invades the surrounding breast tissue, which can lead to metastasis if not treated effectively.

What is the Difference Between Invasive Ductal Carcinoma and Metastatic Breast Cancer?

While invasive ductal carcinoma refers to cancer that has invaded surrounding breast tissue, metastatic breast cancer occurs when the cancer cells spread from the original tumour site to distant organs of the body, such as the bones, liver, lungs, or brain. This spread, known as metastasis, marks an advanced stage and will change the treatment plan and reduces survival rates.

What is the Invasive Ductal Carcinoma Recurrence Rate?

The recurrence rate of early invasive ductal carcinoma recurrence rate varies depending on several factors including stage of diagnosis, tumour grade, hormone receptor and HER2 receptor status as well as effectiveness of the initial treatment. Generally, higher grades and stages of invasive ductal carcinoma have higher risks of recurrence.

Recurrence can happen locally (near the site of the original tumour), regionally (nearby lymph nodes), or in distant organs. Effective initial treatment and ongoing surveillance are critical in managing the risk of recurrence and improving long-term outcomes.

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HER2-POSITIVE BREAST CANCER

HER2-positive breast cancer is a type of breast cancer that tests positive for a protein called human epidermal growth factor receptor 2 (HER2). An excess amount of HER2 promotes the growth of this type of breast cancer.

What is HER2-Positive Breast Cancer?

HER2 positive breast cancer is a type of breast cancer that tests positive for a protein called human epidermal growth factor receptor 2 (HER2). This protein promotes the growth of cancer cells.

HER2-positive breast cancer tends to grow faster compared with HER2 negative ones. However, they often respond well to treatments specifically designed for HER2-positive cancers. These cancers can either be hormone-receptor (HR) positive or negative.

How Common is HER2-Positive Breast Cancer?

Around 15-20% of all types of breast cancers are HER2-positive. It is more common in younger, pre-menopausal women.

What are the Symptoms of HER2-Positive Breast Cancer?

Some patients diagnosed with HER2-positive breast cancer may not present with any symptoms. When symptoms are present, they may include:

  • A new lump in the breast, armpit area or around the collarbone
  • Thickening or hardening in the breast
  • A change in breast size or shape
  • Changes to the nipple, such as sores or crusting, an ulcer or inverted nipple
  • Clear or bloody nipple discharge
  • Changes to the skin including redness, puckering, or dimpling (an ‘orange peel’ appearance)
  • Breast tenderness or pain

If the cancer has progressed to the metastatic stage, additional symptoms may be present depending on where the cancer has spread. Learn more about metastatic breast cancer here.

How is HER2-Positive Breast Cancer Diagnosed?

HER2-positive breast cancer is diagnosed in the same way as most other breast cancers, which typically involves a mammogram and a biopsy. The biopsy is important for determining the HER2 status of the cancer, which helps to guide the treatment plan for the treating doctors. Sometimes the HER2 test is performed on the cancer tissue once it has been surgically removed.

If the breast cancer has spread to other organs, additional tests may be needed to determine the extent and location of the spread.

How is HER2-Positive Breast Cancer Treated?

HER2-positive breast cancer is primarily treated with HER2-targeted therapies. The most common of these in Australia and New Zealand is trastuzumab (Herceptin). The HERA clinical trial found Trastuzumab significantly reduced the likelihood of early HER2-positive breast cancer returning.

Women with early HER2-positive breast cancer may also receive this in combination with surgery, chemotherapy, other HER2-targeted treatments and radiation therapy.

For women with metastatic HER2-positive breast cancer, trastuzumab may be combined with other treatments including other HER2-targeted therapies. This will continue so long as the benefit o the patient outweighs the side effects.

If the breast cancer is also Hormone Receptor-positive (HR-positive), it will grow as a result of the female hormones oestrogen and/or progesterone. Hormone blocking (or endocrine) treatments may also be prescribed in this situation.

What are my chances of Survival (prognosis) if I am Diagnosed with HER2-Positive Breast Cancer?

The prognosis for HER2-positive breast cancer prognosis has improved significantly thanks to targeted treatments like trastuzumab (Herceptin).

Factors such as age, stage of disease, and tumour type greatly impact your chance of survival. Those diagnosed with stage one breast cancer have a 96% chance of surviving five years after diagnosis, while those diagnosed with stage four HER-2 positive breast cancer have over 50% chance of surviving five years after diagnosis of metastatic disease.

Overall, the five-year survival rate for women diagnosed with breast cancer is 91.5%, and 86.4% for men.

What Clinical Trials are Available for HER2 Breast Cancer Patients?

Clinical trials have been vital in advancing the treatment of HER2-positive breast cancer. 

To understand the experience of participating in a clinical trial, discover Laura’s story.

Supporting the latest breast cancer clinical trials today is the best way to change breast cancer outcomes – for you and your loved ones – tomorrow. Donate to improve treatment and save lives.

FAQ’s

Is HER2-Positive Breast Cancer Curable?

With the advancements in treatment, HER2-positive breast cancer is increasingly curable, especially when diagnosed early. The effective targeted therapies, like trastuzumab, have significantly improved the outcomes and life expectancy for HER-2 positive breast cancer.

What Does HER2-Positive Mean?

When a breast cancer is HER2-positive, it means that the cancer cells have an excess of the HER2 gene, leading to an overproduction of the HER2 protein. This overexpression helps the cancer cells grow and divide faster, but it also makes them more susceptible to targeted HER2 therapies.

Does HER2-Positive Breast Cancer Always Require Chemotherapy?

HER2-positive breast cancer treatment often includes chemotherapy, but it is not always required. The need for chemotherapy depends on factors such as size, grade and stage of the cancer. Targeted therapies can sometimes be used in combination with or instead of chemotherapy.

Is it Better to Have HER2-Positive or Negative Breast Cancer?

It is difficult to say whether it is better to have HER2-positive or HER2-negative breast cancer as both types have different treatment approaches and prognosis. However, HER2-positive breast cancer tends to respond well to targeted treatments, which have dramatically improved outcomes for this group.

Is HER2 Breast Cancer Aggresive?

HER2 breast cancer is typically more aggressive than other types of breast cancer due to its rapid growth rate. However, this type of cancer is also more responsive to specific targeted treatments, which can lead to better outcomes than some less aggressive, harder-to-treat cancers.

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EARLY STAGE BREAST CANCER

Early breast cancer is an invasive breast cancer that is contained in the breast and may or may not have spread to the lymph nodes in the breast or armpit. If you have been diagnosed with Stage 1 or Stage 2 breast cancer, you have early-stage breast cancer.

What is Early-Stage Breast Cancer?

Early breast cancer is an invasive breast cancer that is contained in the breast and may or may not have spread to the lymph nodes in the breast or armpit. If you have been diagnosed with Stage 1 or Stage 2 breast cancer, you have early-stage breast cancer.

 Stage 1: A stage one breast cancer means the cancer cells has not spread from the original site to fatty tissues and/or lymph nodes. The tumour will be less than 2cm.

Stage 2: The cancer is larger than Stage 1 and/or has spread to nearby lymph nodes but has not spread beyond the breast tissue or lymph nodes. In stage 2 breast cancer, the tumour is less than 2cm and has spread to 1-3 lymph nodes in the armpit, or the tumour is between 2cm-5cm and has not spread to the lymph nodes.

What are the Symptoms of Early-Stage Breast Cancer?

Some patients diagnosed with early-breast cancer may not present with any symptoms. When symptoms are present, they may include:

  • A new lump in the breast, or armpit area
  • Thickening or hardening in the breast
  • A change in breast size or shape
  • Changes to the nipple, such as sores or crusting, an ulcer or inverted nipple
  • Clear or bloody nipple discharge
  • Changes to the skin including redness, puckering, or dimpling (an ‘orange peel’ appearance)
  • Breast tenderness or pain

How is Early-Stage Breast Cancer Diagnosed?

As stage 1 breast cancer is small, it may be difficult to detect in a physical examination. Often stage one breast cancers are picked up in routine screening mammograms.

Stage 2 breast cancers are slightly larger, with the tumour measuring between 2cm to 5cm, and so it may be felt as a hard lump in the breast or under the arm during a physical examination, or self-examination. Stage two breast cancers are also often diagnosed through screening mammograms.

If early-stage breast cancer is suspected, your doctor may also request you have other scans such as an ultrasound or MRI. A biopsy of the tumour may also be needed to confirm the diagnosis and determine what type of breast cancer you have, which will help to influence your treatment regimen.

How Common is Early-Stage Breast Cancer?

According to the latest data from the Australian Institute of Health and Welfare, approximately 42% of breast cancers diagnosed each year in Australia are stage 1, and 35% are stage 2. New Zealand’s incidence rates are similar. Thanks to the successful BreastScreen Australia and BreastScreen Aotearoa programs, more breast cancers are being diagnosed in the earlier stages which is leading to higher survival rates.

Are there different kinds of Early-Stage Breast Cancer?

Yes. Early-stage breast cancer means that the breast cancer has not spread beyond the breast or nearby lymph nodes. Early-stage breast cancer can be one of four different major subtypes; Luminal A (Hormone Receptor positive, HER2 negative (HR+/HER2-) low grade), Luminal B (Hormone Receptor positive, HER2 negative or positive (HR+/HER2-/+) high grade), HER2 positive breast cancer or triple negative breast cancer.

Your treatment will often depend on what subtype of breast cancer you have.

How is Early-Stage Breast Cancer Treated?

The aim of treatment for early breast cancer is to remove the breast cancer and any cancer cells that may be in the breast or armpit. Treatment may also be needed for cancer cells that may have spread to other parts of the body but cannot be detected.

Treatment can involve radiotherapy, breast surgery, chemotherapy, hormonal therapies, and targeted therapies.

What are my chances of survival (prognosis) if I am diagnosed with Early-Stage Breast Cancer?

Breast cancer survival is sometimes measured in 5-year relative survival. This means how many people diagnosed with breast cancer are still alive five years after their initial diagnosis. Many of those who are alive at 5 years will still be alive and cancer-free for many years after that point.

Breast cancer survival differs and there are many factors that can influence this such as your response to treatment, the type of breast cancer you have, medical history, overall health, age, and tumour growth. You should discuss your personal situation with your doctor and/or treatment team.

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WHAT IS DUCTAL CARCINOMA IN SITU (DCIS)?

Ductal carcinoma in situ, or DCIS, is a non-invasive breast condition which affects around 1,200 women a year in Australia. DCIS is the most common type of non-invasive breast tumour. DCIS is the name for abnormal changes in the cells in the milk ducts of the breast. It is considered non-invasive as it has not spread to any surrounding breast tissue.

What are the Symptoms of Ductal Carcinoma in Situ?

DCIS doesn’t typically present with any signs or symptoms and cannot usually be felt. It also doesn’t present with symptoms sometimes seen in invasive breast cancers. However, if you notice any irregularities in your breast, you should speak with your GP or doctor.

How is DCIS Diagnosed?

Most cases of DCIS are found following routine screening with mammograms and appear as small clusters of calcifications (areas of calcium that can be seen on the mammogram x-ray) that have irregular shapes and sizes. Calcifications can also occur without any evidence of DCIS or breast cancer, depending on the way that they look and are referred to as ‘benign’.

How is Ductal Carcinoma in Situ Treated?

Treatment of DCIS usually involves breast surgery and radiotherapy, and occasionally includes surgery to remove lymph nodes and hormonal therapies. The goal of DCIS treatment is to ensure the abnormal cells in the milk ducts of the breast do not spread and become invasive breast cancer, and to prevent it recurring.

Breast conserving surgery is often recommended for patients undergoing treatment for ductal carcinoma in situ. This is sometimes referred to as a lumpectomy, partial mastectomy, or wide local excision. Mastectomy, or the full removal of the breast, may be considered if the DCIS is widespread in the breast.

After breast surgery, radiation treatment may be recommended to lower the chance the DCIS will come back. If the patient has had a mastectomy for DCIS, radiation is not usually needed.

In addition to radiation, some patients with hormone receptor positive DCIS may take the drug tamoxifen or another hormonal therapy to lower the chance of the DCIS returning. Also, after a diagnosis of DCIS, there is a chance of another DCIS, or breast cancer occurring in one or the other breast, and this hormone blocking therapy helps reduce that risk.

Chemotherapy is not used for DCIS as the abnormal cells are contained in the breast.

DCIS can be treated successfully, and most women diagnosed and treated for DCIS will not develop a recurrence of DCIS, or invasive breast cancer.

Is DCIS Breast Cancer?

DCIS is not considered in the same category as breast cancer, as we more commonly understand it. However, a diagnosis of DCIS can increase your likelihood of developing invasive breast cancer later in life.

Is Ductal Carcinoma in Situ Life-Threatening?

Although these abnormal changes have the potential to turn into invasive cancer cells eventually, a diagnosis of DCIS is not life-threatening as a woman cannot die from DCIS. This is because the abnormal cells are contained within the milk ducts.

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HAND – FOOT SYNDROME

A side effect of some chemotherapy, and targeted therapy treatments, can be hand and foot syndrome, also known as Palmar-Plantar Erythrodysesthesia or PPE. We speak with Senior Podiatrist Rebecca Angus about the symptoms and how it’s treated.

What Is Hand Foot Syndrome?

A side effect of some chemotherapy, and targeted therapy treatments, is Hand Foot syndrome, also known as hand and foot syndrome, Palmar-Plantar Erythrodysesthesia or PPE.

It’s a condition which affects the palms of the hands and soles of the feet, and can also affect the skin on the knees and elbows.

This side effect can make it harder to go about your daily activities, but there are treatments available and methods of reducing your risk of developing this condition.

Hand foot syndrome is a side effect from some chemotherapy drugs. Not all chemotherapy drugs will present with this side effect, but it is important to be aware, so symptoms can be addressed quickly if they appear.

Rebecca Angus is a senior podiatrist with an interest in this condition as she has a personal history of breast cancer, being diagnosed with the disease in 2018. She is also a member of the Breast Cancer Trials Consumer Advisory Panel (CAP).

“I’ve seen a lot of women come through the clinic with these side effects,” she said.

“Hand foot syndrome is a condition that can occur, particularly in women, that are taking taxines and other drugs, such as Xeloda.”

“It’s about the drugs toxicity levels and how high the toxicity level of the chemotherapy is.”

Hand foot syndrome is a skin reaction that occurs when a small amount of the chemotherapy medication leaks out of the small bloody vessels (capillaries), usually on the hands and feet, and damages the surrounding tissues. The severity of this depends on the dosage and duration of treatment.

Unfortunately, it can be a painful condition which can affect your quality of life. However, there are treatments available and ways to prevent this side effect from occurring.

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We speak with Senior Podiatrist Rebecca Angus about the symptoms of hand foot syndrome and how it’s treated.

What Are The Symptoms Of Hand Foot Syndrome?

Symptoms may appear shortly after starting treatment or can occur weeks after. Less commonly, it can occur after being on a drug for months.

Symptoms can include:

  • A lifting of the nails in the hands and feet
  • Peeling or cracked skin
  • Blisters and/or calluses which can be painful
  • Swelling of the hands and feet
  • Infections of the nails
  • Itching
  • Rash
  • A feeling of tightness or stiffness in the skin
  • Numbness
  • Redness
  • Pain
  • Tingling, burning, or itching
  • Difficultly walking or using your hands

How is Hand and Foot Syndrome Treated?

In the first instance, you should make your doctor and/or treatment team aware of any side effects from your treatment. They may wish to change you treatment schedule or dosages to help reduce your discomfort. They may also prescribe corticosteroids to reduce any inflammation.

You may also be referred to an allied health professional like a podiatrist who will work with your treatment team to ensure you can continue with your treatment.

Ms Angus said a podiatrist can work with you to help ease any discomfort and pain, and help reduce the risk of infection or any further issues associated with hand foot syndrome.

“The way we treat it is with general nail care,” said Ms Angus.

“I’m usually trimming the patients nails and if they do have onycholysis (nail detaching from the nail bed), I’m trimming them back.”

“I’m also treating and swabbing for bacterial infections because once you start getting that onycholysis of the nail, you are then exposed to infections,” she said.

“So additional side effects can arise due to an infection, with some patients having to  have antibiotics and stop their treatment, and from my perspective, I would love to see that prevented.”

Other treatment options include using a 10% urea cream on the hands and feet, and regional cooling – using mitts on the feet and hands to prevent peripheral neuropathy and hand and foot syndrome.

Ms Angus said she also educates her patients on the best choice of footwear.

“I ensure my patients have good quality footwear, that actually fit properly, and I use things like neoprene uppers and stretchy materials to try and ensure there is no pressure on the skin.”

“The other thing that I’m doing with patients is making sure their socks are fitting properly,” she said.

“So it’s a process in which they come into the practice, we do that cursory neurological examination, and then we start looking at doing our routine general treatment and then giving them foot-care education afterwards.”

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Ms Rebecca Angus

Rebecca Angus is a Senior Podiatrist working in Sydney and is a member of the Breast Cancer Trials Consumer Advisory Panel. She was diagnosed with breast cancer in 2018.

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BRCA1, CLINICAL TRIALS & SUPPORTIVE COMMUNITIES

Dimity Paul knew she carried an 80% risk of developing breast cancer since she was 21 years old, although it still came as a huge shock when she was diagnosed with breast cancer at 31.

Being BRCA1 & Diagnosed With Breast Cancer At 31

Dimity Paul knew she carried an 80% risk of developing breast cancer since she was 21 years old.

Her mother had been diagnosed with breast cancer when she was a child, and her grandmother had passed away from ovarian cancer.

Dimity’s mother carried the BRCA1 gene mutation and unfortunately passed this down to her daughter.

But Dimity was proactive upon discovering she carried the gene mutation and booked in to get yearly breast MRIs.

“I decided at 21 I wanted to know about my BRCA gene status, so I could make decisions in life and have a small element of control of something that I couldn’t control,” she said.

“I just wanted to make sure that I could give myself the best chance possible going forward in my life.”

Though Dimity was 21 when she received the news that she had the BRCA1 gene mutation, it wasn’t recommended she start screening until she was in her late 20s.

“At 27 I started having a yearly MRI and I had three of those.”

“In one of those MRIs, I had a thing called a PASH that came up, which is an irregularity that’s not a cancer. But then with my fourth MRI, they picked up my cancer.”

Dimity was only 31 years old when she received her breast cancer diagnosis.

“It was a shock,” she said. “And it sounds weird, you know, you have this gene where you have an 80% chance of getting breast cancer, and yet you’re still shocked when you get it.”

Dimity had plans to undergo preventative measures as she got older, however, her diagnosis came before she had the chance.

“You think, I’ll be fine or it’s not going to happen to me or I’ll have all the surgeries before it happens. Because that was definitely my plan.”

“I definitely planned to have a double mastectomy at 35 and my ovaries out at 40. That was the plan.”

“And even though I had that plan, it didn’t go to plan.”

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Dimity Paul speaks with us about her experience with the BRCA1 gene mutation, her participation on the OlympiA clinical trial and how being a part of a supportive workplace helped her through her treatment.

Participating In The OlympiA Clinical Trial

Dimity was diagnosed with triple negative breast cancer.

She underwent chemotherapy, followed by a double mastectomy and a full node clearance.

However, treatment is limited to prevent recurrence in those with triple negative breast cancer.

Though researchers are working to ensure there is new and better treatment options for those with this kind of breast cancer.

The OlympiA clinical trial is one example of this.

The OlympiA trial investigated if the drug olaparib reduced breast cancer retuning in women with early-stage disease, who had a BRCA1 or BRCA2 gene mutation.

Dimity was offered a place in this clinical trial and didn’t hesitate to join.

“Being able to be part of the OlympiA trial was not only about potentially giving me a treatment option, whether or not I got the placebo, it was also a way to contribute to research.”

“So, if I didn’t get the drug, at the very least I’d be helping find the next thing that might be able to treat that next generation of women with triple negative breast cancer.”

Results from the OlympiA trial show that the drug olaparib reduces the chance of recurrence by 42% in patients with early-stage breast cancer who have an inherited BRCA1 of BRCA2 gene mutation. The researchers involved in the study say these results are significant and provide a new treatment option for patients with early-stage breast cancer.

The Benefits Of Participating In A Clinical Trial

There are many benefits to participating in a clinical trial, such as the potential to access a new treatment and helping to further research into breast cancer. Another lesser-known benefit is that those who participate in a clinical trial often get more time with their treatment team.

“It’s like an army of people, and that’s probably the best thing about being on a trial,” said Dimity.

“It’s not just your oncologist, you have a whole team of trial nurses and they were just the best.”

“They are the loveliest people that check in on you and make sure that all of your side effects weren’t really affecting your quality of life.”

Unfortunately, Dimity did experience some side-effects including nausea and fatigue while on the trial, however she said the level of care and attention she received from her treatment team ensured it was dealt with quickly.

She said she worked with her treatment team to find a new nausea drug that worked for her. As this drug caused some tiredness, they decided as a team that it would best for Dimity to take it in the evening so she could continue to work.

“It was collaborative and it really felt like I was part of my care.”

The Importance Of A Supportive Workplace

Dimity continued to work throughout her treatment but said it wouldn’t have been possible if her workplaces were not as supportive as they were.

Dimity changed jobs while undergoing treatment and she said both workplaces went above and beyond to ensure she was supported.

“I travelled a lot for work, and my employer, during my standard treatment, made sure that I didn’t have to travel as much and if I did travel, which I still wanted to do because I still wanted to participate in life, they made it really flexible.”

“So, flexibility is key when you’re going through chemo as you have good days where you can work and you have days where you’re a space cadet, like you have no idea what’s going on and with your workplace just knowing some days they’re going to get ‘good you’ and other days they’re going to get ‘really tired or challenged you’ and they’re okay with that.”

Though Dimity loved that workplace and greatly appreciated the support they provided, she moved onto a new position to progress in her career.

“When I went for an interview with my current job, I was actually still having chemo and I remember in that first initial engagement, I said, oh by the way, I’ve got this cancer thing, but I’m going to be fine, and my potential employer went ‘okay’ and didn’t blink.”

“You can imagine how many people would just say we don’t want to take that risk.”

She said she was called and offered an interview while still in the hospital bed recovering from her double mastectomy. She told them of her situation and asked if they could push the interview back, which they did without hesitation.

She was successful in her interview and was honest about how she was feeling at the time. She told them of her nausea and fatigue and told them how she was dealing with these side effects. She said the organisation was incredibly understanding and her colleagues were respectful of her situation.

“That workplace made my ability to participate in the trial possible.”

“You could have had all the family support in the world, but they’re not sitting there holding your hand at work,” she said.

“Having a supportive workplace is next level because if people can’t afford to go on a trial because they’re not working, we have less participants in trials and we have fewer positive outcomes coming out of them.”

She said having supportive workplaces means those undergoing cancer treatment are still able to remain social through their work, and they’re able to stay financially stable in the present and also in the future.

“You’re helping them stay financially viable, you’re still contributing to their super, which means in retirement they’re not ending up in a really bad situation.”

“I think what a lot of people don’t talk about when it comes to breast cancer, and it comes to cancer in general, is the financial impact isn’t just clinical costs.”

“So, if you can be a workplace and you can be flexible and you can work around a patient, not only will their financial outcomes be better, but you’ll also give them the opportunity to lean in some extra treatments or lean into trials and have better outcomes for everyone in general,” she said.

“You’re part of something bigger when you keep employing someone who’s going through cancer treatment.”

Dimity’s Hope For The Future

Dimity participated in a clinical trial for herself and for the greater good of all breast cancer patients.

She said she hopes to see a reduction of death from breast cancer in the future and understands that clinical trials are vital in that.

“We can’t get there without science, and we can’t get there without patients being willing to participate in the science.”

“So, we need our researchers, we need our doctors and we need our patients all to work together to get to that outcome,” said Dimity.

“One person can’t do it on their own.”

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BRCA-P: TAKING CHARGE OF YOUR BREAST CANCER RISK

Samantha was 21 years old when she found out she had the BRCA1 gene mutation. She speaks with us about her decision to be proactive in managing her risk by joining the BRCA-P Clinical Trial.

Sam’s Experience With The BRCA1 Gene Mutation

Samantha was 21 years old when she found out she had the BRCA1 gene mutation. This means she has a 70% risk of developing breast cancer and a 40% risk of developing ovarian cancer.

She inherited this genetic mutation from her mother, who was diagnosed with breast cancer when Samantha was 12 years old.

“I watched her go through treatment, but because I was so young, I didn’t really understand what was going on,” said Samantha.

“I was about 18 when I found out about the genetic mutation and it was when I was about 20 that I fully understood what was going on and started the process of finding out that I had the BRCA1 mutation.”

At 27 years of age, Samantha decided she wanted to be proactive in reducing her risk of developing the disease. As she was getting older, she had become more concerned about her risk.

“At the start, I was okay with it, knowing that there were options for me,” she said when asked about her reaction to discovering she had the BRCA1 gene mutation.

“But a bit into the future, I started to get a bit anxious about every little pain, thinking it could be something a lot worse than it actually was.”

The options for women with a BRCA1 gene mutation are limited, with the most effective being a mastectomy which involves the surgical removal of both healthy breasts.

“It’s quite an invasive surgery,” said Samantha. “And at 27, it’s not something that I wanted to be doing.”

“I don’t feel that, personally, I was mature enough to have such an invasive thing happen to me.”

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Listen to our conversation with Sam about her experience on the BRCA-P clinical trial.

The BRCA-P Clinical Trial

Samantha’s genetic counsellor knew she didn’t want to have a surgery while still in her 20’s and instead encouraged her to engage in yearly screening to monitor her breast health.

“I had just gotten a phone call saying that my last MRI screening was clear, and from there she explained, that because surgery was off the cards for me, there was a trial I could go on.”

This was when Samantha was introduced to the BRCA-P clinical trial.

BRCA-P is a world-first prevention clinical trial which has the potential to be a game-changer in the way we manage breast cancer risk, by preventing the disease from developing in women with the BRCA1 gene mutation. It’s testing the effectiveness of a drug called Denosumab which has been shown to switch off the culprit cell that gives rise to breast cancer in women with the BRCA1 gene mutation.

Eligibility is carefully assessed for those interested in participating in the BRCA-P clinical trial and includes the following criteria:

  • Women who carry a BRCA1 gene mutation and are aged 25-55 years and unaffected by breast or ovarian cancer – meaning they have never personally been diagnosed with either cancer
  • May either be pre- or post-menopausal
  • Are not pregnant
  • Have not had preventative breast surgery (mastectomy)
  • Not taking any breast cancer prevention agents such as Tamoxifen or an Aromatase Inhibitor

After a physical examination and some blood tests, Samantha was told she met this eligibility criteria. After being taken through the consent forms, and a lengthy discussion with her doctor and support system, she decided she would participate.

Participating in the BRCA-P Clinical Trial

The BRCA-P clinical trial is a randomised, double-blind, placebo-controlled study, which means participants and their study doctor, do not know if they are receiving the trial drug Denosumab or a placebo. A placebo is a treatment that looks just like the active medication but has no effect.

Though Samantha had a 50/50 chance of receiving the placebo drug, she said the benefits of participating far outweighed the possibility she may not receive the trial drug.

“I’m not fazed if I’m on the placebo or the actual medication because I am getting that six-monthly check-up, and that is way more than I would be doing if I was not on the trial.”

“You’re getting the screening, you’re getting the support, you’re getting your questions answered, and that was something truly less invasive than a double mastectomy.”

Samantha is now a year into her participation on the trial.

She said her six-month appointments are very easy and her clinical trial team is very supportive of her, answering any question she may have about the clinical trial.

“So, every six months, I get routine blood tests, just to make sure everything’s all clear.”

“I also get a physical exam and a few little (quality of life) questions that they ask, just to make sure everything’s going okay.”

Samantha also receives her injection of the trial drug at this appointment.

“It’s not painful. It’s kind of a non-event,” she said.

“The injection goes into the tummy, which at first was daunting, but you cannot feel it whatsoever.”

“It’s pretty easy, much less painful than a very big surgery, and it’s also less painful than a routine blood test.”

Trial participants are asked to commit to these six-monthly injections for five years, which Samantha was happy to do.

“Five years is pretty minimal compared to life of being BRCA1 positive.”

Why Samantha is Participating in the BRCA-P Clinical Trial

Samantha said she is very open about her participation with her family, friends, and colleagues. She believes that the more people are aware of BRCA gene mutations and their effect on breast and ovarian cancer risk, the better.

“I feel that the more awareness out there that breast cancer is not an older persons disease and younger people are at risk as well, the better.”

“So I do have an open conversation with friends and definitely colleagues about having the BRCA1 gene mutation and how that affects my risk of developing breast cancer in the future.”

Samantha hopes her participation in the BRCA-P clinical trial, and her openness in discussing this participation, will benefit women now and in the future.

“Whether you have breast cancer now or a have an increased risk of getting breast cancer, the more treatments and preventions that are out there give women more options and control over their life, the better.”

Samantha strongly encourages those who are eligible to consider participating in a clinical trial, and for those who cannot, to support research undertaken by Breast Cancer Trials in other ways.

“The more people backing it up and supporting the research and donating, the more women we can help.”

If you are interested in participating in this clinical trial, head to Breastolution or call 1800 777 253 to find out more.

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WHAT IS PARTIAL BREAST IRRADIATION?

We spoke with Professor Julia White about partial breast irradiation and explore the different types of this treatment, who it is best suited for and the continuing research in this area.

What Is Partial Breast Irradiation?

Radiation therapy, also called radiotherapy, is a common breast cancer treatment used to kill cancer cells and shrink tumours.

However, for some women with breast cancer, studies have shown there is no increased benefit of whole breast irradiation. Instead, they could be eligible to have partial breast irradiation.

Professor Julia White, a tenured Professor of Radiation Oncology and Koltz Sisters Chair for Cancer

Research at The Ohio State University, said partial breast irradiation helps safely reduce treatment for some breast cancer patients.

“Partial breast irradiation is a de-escalation strategy.”

“Historically when breast conservation treatment started, the whole breast was treated.”

“So, instead of surgically removing the entire breast, you remove the cancer from the breast (a lumpectomy), and then irradiate the entire breast and that’s what made the treatment equivalent to breast removal or mastectomy.”

“But we learned over time that women who undergo a lumpectomy alone or lumpectomy plus breast radiotherapy, that the most common place for them to have an in-breast recurrence is around where the original tumour was in the breast,” said Professor White.

“So that really raises the question: do you need to treat the whole breast or can we just treat where most of the recurrence happens and that’s what partial breast irradiation is.”

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We spoke with Professor Julia White, a tenured Professor of Radiation Oncology and Koltz Sisters Chair for Cancer Research at the Ohio State University, about partial breast irradiation.

What Are The Different Types Of Partial Breast Irradiation?

Professor White said there are several different types of partial breast irradiation.

“Accelerated partial breast irradiation is where treatments, usually between five and ten treatments, are delivered in five to eight treatment days, either twice a day or once a day.”

“There’s inter-operative partial breast irradiation that’s done while the lumpectomy cavity is still open prior to closure.”

“And then there’s partial breast irradiation that’s done in a protracted (longer) fashion over three weeks, almost the same time scale as whole breast irradiation,” said Professor White.

“But our focus has really been on accelerated partial breast irradiation that reduces the course of treatment down to five to eight treatment days to reduce burden of care on patients.”

Who Is Best Suited For Partial Breast Irradiation?

Partial breast irradiation is not suitable for all breast cancer patients according to Professor White.

“Like all de-escalation, it’s really focused on luminal type breast cancers.”

“So those breast cancers that are hormone sensitive, lymph node negative, HER2 negative in women who are committed to taking their endocrine treatment for at least five years,” said Professor White.

According to Professor White, partial breast irradiation isn’t considered a ‘better’ treatment option for those patients. But a ‘non-inferior’ treatment option.

“Studies have shown that it’s non-inferior, meaning it will give comparable event rates,” said Professor White.

She said in her clinic at Ohio State University, around 20% of patients are undergoing accelerated partial breast irradiation.

“Particularity women who are still working, taking the time off daily for three to four weeks of radiation is burdensome.”

“They would rather come in and get it done in five days,” she said.

“It helps for women who live far away, they only need to find housing or lodging for about three days if we put the weekend in between and they can travel home on the weekend.”

“We really are catering to a niche group of women who want to keep their breasts, who want a low cancer event rate and who have hormone sensitive HER2 negative stage one breast cancer.”

Partial Breast Irradiation Clinical Trials Research?

Professor White advises that research is still ongoing into this de-escalated treatment.

“There have been several randomised clinical trials looking at the efficacy of accelerated partial breast irradiation, meaning the cancer recurrence rate is the same as with whole breast irradiation.”

“Those trials have all shown that a short course of radiation, in a population of women that are on average about 60 to 62 years old, post-menopausal and arepredominantly stage one hormone sensitive breast cancer, the likelihood of recurrence is very similar to whole breast irradiation. So, non-inferior.”

Professor White said a clinical trial ran at her institution studied partial breast irradiation for women in their mid-50s and younger who had grade three disease.

“We asked the question: can it replace whole breast irradiation and what we found is that partial breast irradiation was not equivalent to whole breast irradiation for that entire group of women undergoing breast conservation therapy.”

“So if you put those two studies together you come up with, I believe, a picture that tells you that partial breast irradiation is a good alternative to whole beast irradiation and will give you similar cancer recurrence rates in women who have hormone sensitive HER2 negative anatomic stage one breast cancer. So their lymph nodes are negative, and the tumour is less than 2cms and women are dedicated to taking their endocrine therapy for at least five years.”

“But that’s a large group of women. That’s probably 25-30% of women undergoing breast conservation.”

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THE CAPTURE CLINICAL TRIAL

The CAPTURE clinical trial aims to improve survival rates for women and men with ER+, HER2- breast cancer. We spoke with the CAPTURE study chair, Professor Sarah-Jane Dawson, about this important clinical trial.

What Is The Aim Of The Capture Clinical Trial?

Around 70% of all breast cancers are oestrogen receptor positive.

Endocrine or hormone treatments for these cancers have been effective, but when the cancer advances, the treatment is no longer effective. Therefore, other ways of treating these resistant cancers are needed.

The Breast Cancer Trials CAPTURE clinical trial is attempting to help find a new treatment for these patients.

CAPTURE is open to women and men with oestrogen (ER) positive, HER2 negative metastatic breast cancer with a PIK3CA mutation, that has returned after treatment with a CDK4/6 inhibitor such as ribociclib, palbociclib or abemaciclib.

CAPTURE is investigating if treatment with a PI3K inhibitor (alpelisib), in combination with fulvestrant, will improve outcomes for patients with metastatic breast cancer when compared with standard treatment.

Medical Oncologist and Breast Cancer Trials researcher Professor Sarah Jane Dawson, is leading this clinical trial in Australia.

She said the study could potentially offer a new treatment option for a significant portion of ER positive breast cancer patients whose cancer has progressed after standard treatment.

“We know that when patients progress on those therapies, their breast cancer is showing resistance to endocrine therapies, and the mainstay of treatment for patients in that situation is often chemotherapy.”

“We’re comparing patients that are going to be treated with alpelisib and fulvestrant, to a group of patients treated with a standard chemotherapy drug called capecitabine.”

“We’re expecting and hoping to see that patients that are treated with the targeted therapy alpelisib will have improved survival compared to patients that are treated with the standard chemotherapy alone,” said Professor Dawson.

However, this clinical trial is only open to patients who carry a specific genetic mutation called PIK3CA.

“So, the CAPTURE clinical trial is looking at trying to identify a group of patients that harbour this genetic alteration, PIK3CA, and make a new therapeutic option available to them in the form of a drug called alpelisib, which is a very specific inhibitor of the PI3K signalling pathway,” said Professor Dawson.

She said potentially eligible patients will be required to undergo a blood test to see if they are carriers of the PIK3CA mutation.

“A novel aspect of the CAPTURE trial is that we’re assessing that information through a blood test. We’re utilising a technology called circulating tumour DNA.”

“Currently, this test is not routine. So, the CAPTURE clinical trial really involves testing to identify the presence of this alteration and to match that with a targeted therapy that hopefully will lead to improved outcomes for patients with this type of breast cancer.”

Though 140 patients will be enrolled onto this clinical trial, many more will be screened to find those with a PIK3CA mutation.

“Oestrogen receptor positive breast cancer is the most common type of breast cancer,” said Professor Dawson.

“Around 40% of patients with ER positive HER2 negative breast cancer would carry a PIK3CA gene mutation in their breast cancer.”

“It’s a large patient group, and we’re hoping this trial will really offer a new therapeutic alternative for those individuals.”

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Listen to our conversation with Professor Sarah-Jane Dawson about the CAPTURE Clinical Trial.

How Can I Get Involved In The CAPTURE Clinical Trial?

Professor Dawson advises patients who are interested in participating in the CAPTURE clinical trial should discuss their eligibility with their oncologist and/or treatment team.

Alternatively, if you have any further questions about this clinical trial, you can reach out to us at Breast Cancer Trials.

Or, if you would like to help support this important clinical trial, you can donate to our life-saving research here.

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SUPPORT SERVICES THROUGH A BREAST CANCER DIAGNOSIS

Being able to access support services after a breast cancer diagnosis is an importance part of the recovery process for some patients.

Why Support Services & Groups Matter For Breast Cancer Patients

Being able to access support services after a breast cancer diagnosis is an important part of the recovery process for some patients, as having access meet and relate with others in a similar situation can aid in alleviating some feelings of anxiety and isolation.

Breast Cancer Network Australia (BCNA) helps to connect those with breast cancer with support services in-person and online.

BCNA Chief Executive Officer Kirsten Pilatti said those who have been diagnosed seek the reassurance and warmth a support group or support person offers.

“I think support is something that everyone needs in very different ways and we know that for many people in Australia, they want to join support group.”

“Women say that they want to connect with someone else who’s made it through treatment, and who’s made it twenty years past their diagnosis.”

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Listen to our conversation with BCNA’s CEO Kirsten Pillatti about the importance of support groups and services.

While BCNA helps to connect those recently diagnosed with in-person or online support groups and services, they also provide an online tool to help those recently diagnosed.

Ms Pillatti notes this is especially helpful for those who may not feel up to a group support setting.

“The My Journey online tool helps people to navigate a really complex system” said Ms Pilatti.

“What I hope is that we can continue to build the resources that we have to help people in the way that’s right for them.”

“The way we helped and supported people ten years ago is very different to how we support people now.”

“Everyone’s breast cancer treatment options are so different, so we need to provide a really tailored support program for people and it’s tricky” said Ms Pilatti.

“But we want to be there for every Australian and we want to make sure that we really are the voice for the people who find it hard to be connected and supported in their local communities.”

You can learn more about connecting with a support group in your area, or the online My Journey tool at bcna.org.au

 

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ESMO 2021: BREAST CANCER RESEARCH SUMMARY

The latest research and advancements in cancer treatment, prevention and care are presented at the ESMO Congress.

European Society of Medical Oncology Congress (ESMO) 2021

For the second year in a row, the European Society of Medical Oncology (ESMO) has held its annual Congress online, allowing researchers and clinicians worldwide to connect despite travel restrictions in place due to the ongoing COVID-19 pandemic. The ESMO Congress is one of the largest and most important cancer conferences worldwide, and brings together around 30,000 clinicians, researchers, patient advocates and healthcare industry representatives from approximately 140 countries.

The latest research and advancements in cancer treatment, prevention and care are presented at the ESMO Congress, which allows medical professionals to work together and translate these results into better patient care worldwide.

We have collated some of the important breast cancer research presented at ESMO 2021 and provided a summary below:

DESTINY – Breast03 – A Phase III Clinical Trial For Metastatic HER2 Positive Breast Cancer

Results from the DESTINY – Breast03 clinical trial showed a statistically significant improvement in survival without worsening of cancer, for patients with metastatic HER2 positive breast cancer. These promising initial results are expected to lead to a new standard treatment for patients with HER2 positive metastatic breast cancer.

Currently the first-line standard treatment for patients with metastatic HER2 positive breast cancer is HER2 antibody therapy with pertuzumab/trastuzumab, plus chemotherapy. If the cancer worsens, the treatment will often switch to trastuzumab emtansine (T-DM1) which is an antibody-drug combination comprised of trastuzumab and a chemotherapy drug.

DESTINY-Breast03 is a global clinical phase III clinical trial evaluating the safety and efficacy of a drug called trastuzumab deruxtecan (T-DXd) compared to the current standard treatment of T-DM1 in patients with HER2 positive metastatic breast cancer who have received two or more prior anti-HER2 based treatments. TDX is a HER2-targeted antibody that delivers high concentrations of chemotherapy directly to cancer cells that have excess HER2 receptors on their surface.

Results from DESTINY-Breast03 showed treatment with T-DXd led to a 72% reduction in the risk of disease progression in comparison with treatment with T-DM1. 12-months after starting treatment, 76% of patients who received the trial drug T-DXd had no evidence of cancer worsening, compared with 34% of patients in the control group who were receiving T-DM1. As well as improved progression-free survival, 80% of those receiving the new T-DXd treatment saw their tumours shrink compared with 34% on the control group being treated with T-DM1. Additionally, 16% of patients treated with T-DXs had their disease completely disappear on scans. Side effects were generally mild and manageable, with no substantial differences between groups.

These results show that treatment with T-DXd is significantly better than T-DM1 for patients whose cancer has progressed after treatment with trastuzumab and chemotherapy. Overall survival results will be reported in the near future.

Researchers conducting this clinical trial have suggested that this positive result will likely change the standard treatments for patients with metastatic HER2 breast cancer whose disease has progressed after first line treatment. Next, researchers will investigate the benefit of treatment with T-DXd in the first-line metastatic setting, and for those with early-stage disease.

MONALEESA-2 Clinical Trial: Improved Survival for HR Positive, HER2 Negative Advanced Breast Cancer

In late breaking results presented at ESMO 2021, the MONALEESA-2 trial showed adding a CDK 4/6 inhibitor to first-line hormonal treatment prolongs survival by one year for post-menopausal women with HR positive, HER2 negative advanced breast cancer.

The MONALEESA-2 clinical trial allocated 668 patients to take either ribociclib, a CDK 4/6 inhibitor, plus the aromatase inhibitor letrozole or to take placebo plus letrozole. Patients who had previously received a CDK 4/6 inhibitor, chemotherapy or endocrine therapy for their advanced breast cancer were NOT included in this study.

Patients on the trial drug combination had a statistically significant and clinically meaningful improvement in median survival at 63.9 months survival compared with 51.4 months on the standard care arm. Follow-up at six and a half years, the longest for any CDK 4/6 inhibitor trial to date, showed that patients who took the new treatment lived for one year longer than those who took letrozole alone. MONALEESA-2 also showed that after five years, patients treated with ribociclib plus letrozole had more than a 50% chance of remaining alive. This drug combination maintains quality of life, without major side effects.

This treatment combination is currently in use in Australia in this patient population based on earlier results of this and other trials. These results give greater promise for patients diagnosed with advanced HR-positive breast cancer.

Research and analysis are continuing to determine if there were any specific groups of patients in the study that benefitted more or less from this treatment. The study researchers have told the ESMO 2021 audience that this is the first CD4/6 inhibitor to demonstrate an overall survival benefit in this first-line patient population so far, but they are still awaiting results for clinical trials investigating other CDK 4/6 inhibitors palbociclib and abemaciclib (such as the BCT PATINA clinical trial).

Triple Negative Breast Cancer Research

The BARBICAN Clinical Trial for Women with Triple Negative Breast Cancer

The BARBICAN clinical trial is a randomised phase II study which is aiming to determine the contribution of the drug ipatasertib to neoadjuvant chemotherapy plus atezolizumab in women with early stage triple negative breast cancer.

144 patients took part in this clinical trial, with an equal number receiving the trial treatment of ipatasertib with atezolizumab and chemotherapy, and atezolizumab and chemotherapy alone. Unfortunately, there was no difference in pathological complete response (pCR) between the two groups.

While this result isn’t what the researchers were hoping for, ipatasertib is being used in other clinical trials for different types of breast cancer. Further analysis of this and other trials using this drug will look at blood and cancer samples to find if there is a marker to indicate a group of patients more likely to benefit from it. Not every treatment is suitable for different types of breast cancer, and researchers often trial drugs across several different breast cancer types and stages to find where it can work best. So, while there was no clinically significant result found in the BARBICAN clinical trial, this does not mean ipatasertib will not benefit other breast cancer patients.

For example, the Breast Cancer Trials FINER clinical trial, due to open to patients in 2021, is looking at using a combination of ipatasertib and fulvestrant for patients with metastatic or advanced ER positive, HER2 negative breast cancer which has grown or spread despite treatment with a CDK4/6 inhibitor and an aromatase inhibitor. Our researchers are hoping this combination will help to keep the cancer under control for longer.

BrighTNess Clinical Trial: A Triple Negative Breast Cancer Trial

Long term follow-up of the phase III randomised BrighTNess clinical trial has shed light on what works, and what doesn’t, when treating early stage triple negative breast cancer.

Initial results from the trial showed that the pathological complete response rate (the disappearance of all invasive cancer in the breast) was significantly higher among participants who were assigned to receive veliparib (a PARP inhibitor) plus carboplatin (a chemotherapy drug) alongside paclitaxel (another chemotherapy drug) compared with those given paclitaxel alone. However, the rates did not differ significantly between patients who received all three treatments, to those who received the combination of the two chemotherapy drugs. In other words, the improvement appeared mostly due to carboplatin chemotherapy at that early time point.

Results presented at the ESMO Congress 2021 were from a median follow-up of 4.5 years and backed up these initial findings. The likelihood of remaining alive and cancer-free at four years was 78.2% for those who received all three drugs, 79.3% for those who received the carboplatin and paclitaxel, and 68.5% for those who received only the paclitaxel.

The study researchers concluded that their findings support the inclusion of carboplatin in neoadjuvant chemotherapy for stage II-III triple negative breast cancer. This is a topic that doctors have been debating for some time, and should help resolve that debate.

Results for the KEYNOTE-355 Clinical Trial for Metastatic or Inoperable Triple Negative Breast Cancer

The final results of the KEYNOTE -355 clinical trial show that there is a significant overall survival benefit to adding pembrolizumab (an immunotherapy drug) to chemotherapy for advanced triple negative breast cancer.

These final results show that the patients who received pembrolizumab plus chemotherapy had a median overall survival of 23 months, versus 16.1 months for those patients on placebo plus chemotherapy. The combination of pembrolizumab and chemotherapy reduced the risk of death by 27%. The benefit appeared restricted to patients whose tumours had higher levels of the PD-L1 tumour marker. The researchers involved in this study said this is an important result as it’s the first study showing overall survival benefit in the metastatic setting for this poor prognosis type of breast cancer. Immunotherapy has yet to become incorporated into routine practice in breast cancer in Australia, however that may well change after these results.

COVID-19 & Cancer Research

OnCOVID Study: 15% of Patients with Cancer Experience ‘Long Haul’ COVID-19

A study which drew patient data from 35 different institutions across six European countries from February 2020 to February 2021, found that one in six cancer patients who recovered from COVID-19 experience long-term effects, or ‘long-COVID’. It has been increasingly recognised that people who contract COVID and then recover from the acute effects may experience ill effects for months or longer afterward. Cancer patients are more likely to contract COVID, and also more likely to become sicker or die as a result.

The OnCOVID study results presented at ESMO 2021 found that 234 cancer patients (15%) had at least one post-COVID-19 complication. The most commonly reported problems included respiratory problems (49.6%), fatigue (41%), neurological or cognitive issues (7.3%) and weight loss (5.6%). Factors associated with an increased risk of ‘long COVID’ included being 65 years of age or older, two or more other health problems, a history of smoking, increased rates of prior complicated COVID-19 and requiring therapy and/or hospitalisation for COVID-19.

Patients with cancer (or a history of cancer), are recommended to receive their COVID vaccine after a discussion with their doctor(s). Cancer Australia has up-to-date information about COVID-19 for those affected by breast cancer, and a comprehensive list of FAQs about the COVID-19 Vaccine for those with cancer, noting that all adults in Australia and New Zealand are now eligible to receive a COVID-19 vaccine.

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