Multiple Myeloma - Survival Rate Statistics by Hospital
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No Respect!  Myeloma Patient's Don't Even Get Credit For Dying!  Do The Myeloma Math.

2/29/2016

15 Comments

 
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This a subject I have thought of writing about for a very long time.  When we lost Pat Killingsworth recently it brought it back front and center for me.  Pat has had a 9 year battle with a rare presentation of multiple myeloma.  In the end he died from a brain aneurysm, aggravated by a rare form of blood disorder called TTP, and TTP was most likely caused by the chemotherapy from his myeloma fight.  He was admitted into the hospital with kidney failure.  So what was on his death certificate, kidney failure, brain aneurysm, TTP, or complications from chemotherapy, or complications from multiple myeloma.  Well, it was listed as a brain aneurysm. I am fairly certain Pat would say he died from complications due to myeloma.  This would be important to him because funding for the NCI(National Cancer Institute) uses lives lost in there allocation of funds.   So if Pat, a myeloma patient and fervent myeloma advocate, can not be considered part of the myeloma death statistics then who can.  Let's take a look at the math.  The National Cancer Institute reported the following:

  • Estimated New Cases in 2015 -  26,850 
  • Estimated Deaths in 2015        -  11,240

This would suggest the cure rate would be (26,850-11240)/26,850  =  58%, however the long term survival of myeloma patients is only 10 to 15%.  It can therefore be deducted myeloma deaths are under-reported by over 43%.  Because the most likely causes of death for myeloma patients is  pneumonia, infection, and bleedouts, these could easily be on the death certificates of many myeloma patients.  So if cure was 15%, then the number of deaths would be closer to 22,822.   Why is this important for the myeloma patient community?  The NIH (National Institute of Health) and NCI (National Cancer Institute) use deaths, and lost years of life by cancer type to rationalize the research spending for the NCI research projects.  The more deaths and  lost years of life the more spending for that form of cancer.  A study by the NIH tries to rationalize spending to the number of lives lost and years of life lost by cancer and you can read it if you CLICK HERE.  A summary slide is shown below. 


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The way to read the graph is that for prostate cancer, NCI funds three times more than the YLL(years of lost lives due to prostate cancer) can justify.  It also shows myeloma gets about 8/10 of what it should get based on its reported YLL, but we know myeloma deaths are being underrepresented.  If represented correctly the myeloma spending falls to about 1/2 of what is justified by its real YLL.   Great for leukemia which 2.2 times what its YLL would justify or lymphoma, which gets 1.4 times what its YLL would justify.  But as is the title of this post, "Myeloma Gets No Respect".  This graph shows how out of balance the spending is to the lost years of life by cancer type, and I hope the NCI uses this study to better balanced spending.  In addition, the deaths should be computed by taking the newly diagnosed number and subtracting out the projected cure rate.  Most other cancers seem to closely follow this formula when you look at the reported newly diagnosed and deaths shown on the NCI SEER web site.

We spend $124 billion on cancer treatment each year and fund the NCI with just $5 billion.  To me this is penny wise and pound foolish.  Maybe we should be funding everything at 3 times the current average funding instead of cutting anything.  That would just be $15 billion, and one would expect a much larger reduction in cancer treatment cost to offset this in the longer run.   That would mean myeloma would end up with 7 times the current amount if everyone got their YLL share.  Wishful thinking,
dreamer, yes, but reasonable and logical. 


For more information on multiple myeloma CLICK HERE and you can follow me on twitter at: https://twitter.com/grpetersen1

15 Comments
Robert Lewy
2/29/2016 07:27:41 am

Well said. Gary. It does matter that death certificates are accurate

Reply
Gary Petersen link
2/29/2016 09:21:11 am

Robert, Patti checked on the reported cause of death and had them change it from aneurysm to complications from myeloma. She knew Pat would have wanted this.

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Eric Hansen
2/29/2016 08:57:14 am

Well said, Gary! Completely agree. How the determination of cause of death is made matters a lot. But often it seems the attending physicians have little or no history with their patients at this time. So they go with what seems obvious--but isn't reality. I'm going to discuss this with my medical team so we are all on the same page- hope it works........many years from now?.........

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Gary Petersen link
2/29/2016 09:24:19 am

Eric, as a informed patient like yourself and your own best advocate, it is going to be "many years from now!". Patti made sure it was reported as she knows Pat would have wished.

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Victor Thuronyi
2/29/2016 11:37:34 am

Gary,
While you assert that myeloma deaths are underreported, I don't see any evidence in your article for that. What is the methodology by which the NCI calculates the munber of myeloma deaths? We should find out. Maybe you are right, but I am not sure.

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Gary Petersen link
2/29/2016 02:29:40 pm

Victor, the NCI obtains there mortality information from the National Center for Health Statistics. You can see a overview of the SEER data at the link: http://seer.cancer.gov/about/overview.html
My assertion is based on the logic that the deaths should equal the number of newly diagnosed - the number of projected cured. This holds true for most cancers which are within 10%, but is 48% off for myeloma. Gary

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Dianna Chiles
3/1/2016 07:52:16 am

Thank you Gary for continuing to write about the issues for Myeloma patients. Keep up the good work.
Thank you to Pattie Killingsworth for changing cause of death for Pat. It is the various treatments that ultimately cause one to lose the fight against this very difficult disease to treat.

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Gary Petersen link
3/2/2016 10:06:56 am

Thank you Diane, hope you are fleeing better. See you at the next IMF support group meeting.

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Ray link
3/3/2016 07:18:28 am

Maybe there's an assumption that the rate of all cancer related deaths are equally unreported in a similar way. I don't know that myeloma is that unique in that way. There are some where yes the cancer kills you directly but others are similar to myeloma. One should look at all the numbers to accurately compare. Hopefully it's fixed some day but it should be fixed for all and not just one.

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Gary Petersen link
3/7/2016 04:13:24 am

Ray, great idea, and it can be done. Newly Diagnosed can be adjusted down by the number cured and also adjusted for the average age of each cancer type to get a New Relative Survival number. Even with this method it would show myeloma is the one cancer that is grossly underreported.

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JES
3/6/2016 05:38:16 am

we are completely devastated by the untimely loss of my father, who was so careful with his health that he surely had some good years ahead of him. Unfortunately, I watched my father slowly dying with his declining condition in the past few years as multiple myeloma progressed undiagnosed.
My father , himself a physician, trusted and believed in his providers, never questioning their care... until the end. At which point, it was too late. A simple blood test, a simple "connect the dots" of his condition would have meant life for him and a father for us to enjoy for a few more years. His tragic
loss due to avoidable kidney failure should serve as a caveat to us all....
there is nothing more bitter than to call the doctor and request the test for multiple myeloma myself as it was not ordered years, months or even days before.

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Donna C link
3/7/2017 09:41:52 am

This makes me so sad.

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Gary Petersen link
3/7/2016 04:18:32 am

So sorry for your loss. Stories like yours are all too frequent. Myeloma UK reports 20% of patients die within the first 2 months of diagnosis. I believe many of these could have been prevented by a good GP. Sometimes I think it is gross negligence and may require a legal remedy. Gary

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David Langston
3/8/2016 09:48:47 am

As I understand it, no one really dies of myeloma. The big three killers are respiratory infections, sepsis, and kidney failure. A fourth killer group is sort of a miscellaneous grouping, but even in aggregate is smaller than the big three. That said, it is understandable how death certificates might not identify correctly myeloma as the primary cause of death in all cases.

Speaking of death caused by kidney failure, I'm of the belief that as long as you continue to undergo proper dialysis, minimize fluid gain, and maintain proper electrolyte and albumin levels, there can be no death by kidney failure. This doesn't rule out other fatal secondary complications from dialysis though. I suspect that most or all reported deaths by kidney failure are simply due to withdrawal from dialysis treatment. This goes for all dialysis patients, not just those with myeloma.

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Jean O link
3/4/2024 11:30:04 pm

Very informative article. Thank you for making me aware of this. It makes me question what they truly base funding on.

I do not know how MM rates as far as expense goes in relation to other types of cancers. It must be fairly high based upon the medications and treatments my husband has received so far. I have also read about the disparities in obtaining a diagnosis. Even more so, the disparities in treatment and care. Before reading this, I would have thought these disparities would have contributed more to this than lives lost.
I advocate very strongly for my husband or at least have been told this more than once. I am sure I have unintentionally ruffled a few feathers along the way. I have been told several times that I ask difficult, but well thought out questions. We have had some sticky situations because of this which has caused us to get second opinions and once a different center all together. I try not to be demanding or intimidating with my questions and always try to find answers myself before asking the doctors. I have asked doctors to change or correct things in their notes which I feel are misleading or just flat out wrong. I have more respect for a doctor who tells me he doesn't know an answer, looks it up, corrects or explains something in his notes versus ones who have answers for everything.
I mention this because I feel most family members would say their loved one died from multiple myeloma or cancer before an anyursym

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