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Sentinel Node Biopsy

I was diagnosed with breast cancer in November 12. My first reaction to this was shock and disbelief as there was no previous history in my family.

Nancy - Aged 42

My name is Nancy. I am 42, married to a wonderful and supportive husband with two beautiful sons aged 10 and 12. I was diagnosed with breast cancer in November 12. My first reaction to this was shock and disbelief as there was no previous history in my family. I later learnt most breast cancers detected are not hereditary.

My treatment options were to have either a lumpectomy or mastectomy and axillary dissection, possibly followed by radiation therapy, chemotherapy and/or hormonal treatment depending on the outcome. My greatest fear was having the axilla dissected and the possible side effects of lymphoedema. I was resolved to having surgery to the breast but felt I needed more information about lymph node removal. This may appear a minor issue compared to having a life threatening disease but I am right-handed and my right arm would be affected.

I found a surgical oncologist who performs sentinel node biopsy, a procedure that identifies and removes the first lymph node to which the breast cancer cells might spread. The surgeon provided lots of information to read about sentinel node biopsy. I decided to proceed with it. Unfortunately my sentinel node contained some cancer cells and the recommended treatment was axillary dissection. I still felt uncomfortable with this and found there was another option for me, to enter a clinical trial being conducted at Peter MacCallum Cancer Institute. This trial was part of an international study by the American College of Surgeons Oncology Group - a randomised trial of axillary node dissection in women with a certain clinical breast cancer who have a positive sentinel node. I was a possible candidate.

My husband and I discussed the options. One was to have an axillary dissection, the other to take the risk against medical advice and not remove any more lymph nodes, the third to enter the trial. If I entered the trial and was chosen not to have the axilla dissected I would have the advantage of being closely monitored. This would be the same if I had the axilla dissected. I had to feel comfortable with someone else (a computer!) making the choice for me.

After careful consideration I decided to participate. I signed up, my details were entered into the computer and within seconds the decision was made to have the axilla dissected. It was only then I knew I had made the right decision. I had my surgery and found I had no other lymph node involvement. Of the 20 removed there was only one lymph node involved. With hindsight I would not have needed to have further surgery.

I believe this justifies my participation in the study. Peter Mac is hoping to recruit 15 Australian participants for this trial. I was only the second. I hope that very soon the Australian Standard for every woman with early stage breast cancer is to undergo sentinel node biopsy.

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In hindsight I might have chosen the sentinel node biopsy. You should at least consider it.

Russ had a choice of sentinel node biopsy. She decided to have all her lymph glands removed. They were all clear.

I was offered the sentinel node biopsy. Put very simply it is a procedure where a dye is injected into the lesion(s) and some time later is viewed under a scan (as it is radio-active) It is thought that the dye will track to its corresponding axillary node if the cancer has spread to the axillary glands. This is a pre-operative procedure, that is, on the day of the breast surgery, prior to the removal of the breast cancer.

Depending on the results of this procedure the glands in the armpit may not be removed at this time. However, some days later a second operation may be necessary to remove these glands if the more detailed pathology shows the sentinel node is malignant . This then requires another anaesthetic and the extra surgery for the removal of the glands.

After a lot of consideration I chose to have all the glands removed at the time of the removal of the two malignant lesions. Why I am relating this experience is to say that I need not have had the glands removed as they all were free of cancer – in hindsight I had made the wrong decision. I do not have regrets at this decision, as having an extra anaesthetic was an important point is my decision and other factors came into it also.

It is a procedure not adopted yet by the Royal College of Surgeons. As part of a trial, surgeons are removing all the glands and the data is being collected for a time and numbers assessed to see if Australian doctors will offer it to us here in Australia. It is being, and has been used overseas for some time. Some opinion is that we, here in Australia adopt a more aggressive role in removing all axillary glands when an unknown number of breast cancers do not require this removal of the axillary nodes.

One of the side effects of breast surgery with removal of these glands, can be lymphodema, with varying degrees of severity. So to get an opinion from a surgeon who offers this alternative –if it is appropriate to your particular breast cancer, I feel is worth knowing. My first surgeon I saw and whom I chose to do my surgery did not mention it to me- I found out about it from another information source. I did tell him I had seen the other doctor, had considered the other information in coming to my decision to have him do the surgery. Without being conversationally confronting he gathered I would have been pleased to have him tell me that there were other doctors, who do feel women should be informed of this alternative practice.

One last thing I have learnt from this cancer experience – but not everyone is the same as I,- is that we cannot have too much information in making what is the best decision for us. But everyone who attended a workshop conducted recently by the NSW cancer Council –20 to 30 odd people who had experienced various cancers, all emphasized the necessity of getting copies of all pathology results and keeping them forever with all your treasured possessions. Cancer science and treatment is forever changing and hopefully progressing with better outcomes for people with cancer and you need to know as much as possible in the detail of your particular cancer. I hope sharing “ my story” may be helpful to someone out there and that you too may find a person to walk with you during your cancer experience. I consider myself so fortunate in having my friend to support and share it with me.

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I chose Sentinel Node Surgery to maximise my chances of maintaining my preferred lifestyle after treatment.

Caroline - Aged 38

Caroline had just moved into a new home with her newly found partner. "The home was a "renovators delight" that backed onto bushland near the river. We were so excited about landscaping, building and canoeing on the river. We both love the outdoors. News of the cancer was shock enough without learning of the possibility of lymphodema as a side effect of treatment. If I had to avoid camping, insect bites and exposure to the sun, then we would probably have to move and our planned future lifestyle together would have to be dramatically altered".

Caroline was fortunate to have been referred to Dr Paul Crea who had just completed trials on the Sentinel Node Procedure. "While the risks were slightly higher that the full axilla clearance technique, it made a lot of sense to me. If it turns out the nodes are not likely to be affected - why remove them all and face the possible resultant side effects".

Caroline was very lucky. The sentinel node biopsy was clear and so surgery was minimal. "Within a week or two I had full movement in my affected arm and now I am back to canoeing, camping and travelling with work without concern. The cancer diagnosis, surgery, chemotherapy and radiotherapy all have a huge impact on your life as it is, and it's a fantastic breakthrough to have new procedures like this that improve your options and reduces the side effects".

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