Reporting Death by Treatment
Comments
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I just lost a friend recently diagnosed with grade 3 stage 3 IDC. She died from sepsis due to chemo lowering her WBC. This was the second person I knew who died from breast cancer treatment. My sister was the first. She had IDC and lymphoma at the same time and developed MDS, which killed her, due to all the radiation she had for the other two.
Neither was malpractice, both had capable doctors. My friend was having chemo prior to surgery.
We always hear that these cases are rare and I don’t believe they are as rare as the medical community would like us to believe. I was definitely mutilated, poisoned and burned in 2003 and suffered again in 2019 from wounds on my breast reconstruction, failing to heal properly due to prior radiation. I survived but it doesn’t make the treatment right. Thankfully in my case we now have tests like OncotypeDx that give a better indication of who will benefit from chemo. I don’t believe I needed chemo in 2003, but they didn’t have the Oncotype test then.
I plan to put everything I feel right now, the profound sadness, anger and frustration, to better use in the new year and work to raise funds for research for better, less harmful treatments.
I would like to know if death by treatment is reported to any breast cancer agency or are these lives hidden in in medical red tape? I am guessing that unless they are part of a study, they aren’t recorded as having died due to cancer treatments. Maybe it depends on the state? Maybe the medical community feels this is such a rare occurrence that they are morecomfortable not reporting these deaths as treatment related? I have a feeling due to the cause of death being recorded as sepsis, or organ failure, death from treatment is greatly under reported.
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I am so very that you have lost such dear people in your life. I doubt anyone that died from treatment or overtreatment has that listed as cause of death. That's just my opinion.
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My twin sister died (in 2008) from her first dose of Ixempra (in addition to Xeloda.) She had a choice of just Ixempra or both, but chose both because her oncologist said it should work better with the combination. She had been on chemo for almost 4 years and tried many chemos. Avastin worked for at least 2 years, but they stopped giving it to her after a study that said it didn’t extend overall survival. Her tumor markers steadily inclined after that and Ixempra had just come out so she was willing to try anything at that point. The chemo did not clear out of her body and she was in ICU for a week before she passed. It was horrific and I believe part of the problem was that she was on an anti fungal that was contraindicated. I shared this with her the night before chemo and she asked about it, but the oncologist said that it should be okay. I have no idea what was listed as the cause of death.
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Hi, Tamoxifen nearly killed me in four months. I am one of the 2.9% of women that have a hepatotoxic response. You hear about the 5% that get uterine cancer but not the smaller fraction that it nearly kills. In my case I was grade 3 obese (260lbs and 6ft tall) going into BC. I had a mildly fatty liver but all liver enzymes were normal. I had surgery and radiation with Tamox overlapping the radiation. I went from a normal functioning liver to stage 4 decompensated cirrhosis in just less than four months. I now need a transplant and that is another trip in frustration. In March (surgery date) I will be two years out but you need to be 5 years out to receive a transplant (medical ethics.) My liver will at best hang on until I am three years out at which point my doctor says 'we will have a conversation.' Both of my sons are a match thankfully as with a history of cancer I cannot receive a cadaver liver. This topic is great as my breast cancer was the best case scenario in the sense that it had not spread and was contained to the breast with an Onco of 17 but the cure nearly killed me and might yet succeed. I am angry. My transplant doctor that is monitoring me is angry too as he says more women are going into breast cancer obese (I can give you many excuses like menopause which was a ride and caring for a Mum with dementia, and a demanding job, and a sweet tooth, and a husband with lung disease and on and on) but my doctor feels that it should be standard protocol to ultrasound overweight women for the first 6 months every two months when starting Tamox then every 6 month thereafter. But my Onco says they don't want to scare women off of the treatment. I would have liked to have been informed. Mine was acute onset with ascites (fluid in the abdomen that had to be drained--not fun, and hepatic encephalopathy where ammonia not broken down by my liver crosses the blood brain barrier and you go loopy, and jaundice. The texture of my liver also changed and is now covered in nodules. It also gives me an annual 20% chance of hepatic carcinoma. Yipee! So the bottom line is---I SHOULD HAVE BEEN GIVEN THE CHOICE TO HAVE MADE AN INFORMED CHOICE.
Cheers, Liz
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Oh Liz. That is so completely fucked up. No other words can possibly cover that. I will not sanitize it either.
You deserved to 100% know, and should have been given a fully informed choice.
Shame on your oncologist.
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Thank you for not sugar coating my reality. It sucks. I should add that approximately 40% of women on Tamoxifen will get a fatty liver and not necessarily from obesity. Tamoxifen can induce a fatty liver but when given to women with an already fatty liver it can race you to the finish line for liver disease. I realize that it has saved so many lives but all of the risks should be disclosed from the outset. I am doing everything I can to hold on--I have lost 100lbs, 1000mg/day of sodium and not a gram more, fluid restriction to 1 litre/day, I take the meds, I am tolerating Letrozole well for the BC, I drink this vile protein powder daily as malnutrition due to malabsorption is a thing with a broken liver and it also helps to fight muscle wasting, I suffer the debilitating cramps you get with liver failure and all because I wasn't monitored for liver function decline. So pissed off. I was given a bottle of Tamoxifen and told see you in 6 months. I called the clinic and said I'm getting sicker and was told the side effects would settle down. I called again when my belly started to swell and was told Tamoxifen can cause abdomen bloat. I called again when I just felt awful and was told to call my family doctor as I might be suffering depression. I have been left feeling like I wasn't worth the effort. Now, however, they have rolled out the red carpet for me and nothing is too much to ask. Too little too late. I just need to hang on. I just pray the BC doesn't return as then I am well and truly fucked as my damaged liver can't tolerate chemo. And also, if the BC returns I can't have a transplant. The super stupid cherry on the cake is if I do get liver cancer that is not mets from the original BC I can have a transplant but if I have mets from BC I get a palliative ride to death and no transplant. So I pray I stay well enough for a transplant, get it, the breast cancer never returns and I live a well life.
Here's hoping anyway.
Cheers, Liz
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CanadaLiz, that is appalling and terrifying. I get CT scans about three times a year because I had breast cancer and kidney cancer at the same time. My latest scan did show a fatty liver - and I started Tamoxifen around the first of the year. When I had my surgeries, I was overweight, but now I'm obese because my weight had been down due to one or both cancers, and since I stopped smoking before the nephrectomy, it added to the weight resurgence. I assumed the liver issue had more to do with losing a kidney, since my kidney function has fluctuated in the last year. I see my primary doctor tomorrow, and my oncologist in January - now I've got some very direct questions to ask them.
Wishing all the best for you until you can get your transplant. ❤
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i haven been taking tamoxifen for 4 years. my liver blood work has been up and down. Just got my results today and they are higher than ever. I had my surgery 4 years ago diagnosed with dcis stage 0 breast cancer. Did radiation. Is anybody else having the same problems. i have joint pain all over. please help.
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Dear fernanda08,
Welcome to the BCO community. We are sorry for your diagnosis and treatment side effects but glad that you reached out. We are thinking that you might be better to post this question in the Hormonal Therapy Forum. There are a number of topics there about Tamoxifen where you can post or start your own. Hopefully you will get some ideas there.
The Mods
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Fernanda08, my fatty liver showed up on my latest CT scan, but my bloodwork has been okay. Not sure if this is normal. Heck, I don't know what anything normal is at this point!
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