Multiple Myeloma - Survival Rate Statistics by Hospital
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Multiple Myeloma - The younger you are, the better the prognosis!   A much improved life expectancy and survival rate!

10/16/2012

31 Comments

 

One of the fundamental understandings of multiple myeloma is that the younger patients do have a better life expectancy than the older patients.  This has been thought to be because the younger patients have stronger immune systems to begin with, and do not have the co-morbities (other illnesses) that come with age.  In addition, they are generally more able to take the trauma of chemotherapy and transplant.  It is common knowledge, but I have not been able to find the data anywhere that quantifies the difference.  That is until recently.  

In my research I came across a study by the United Kingdom's National Health Service.  The study data can be found at the following link: http://www.cancerresearchuk.org/cancer-info/cancerstats/types/myeloma/survival/  Because the UK has a national health system, they have some of the most robust data for most any medical condition.  The reporting of survival data is built into the system.  Whereas, we in the USA have to rely on our National Cancer Institute to obtain information, or for other private organizations like the CIBMTR (Center for International Blood and Marrow Transplant Research) to obtain this multiple myeloma data.   I therefore think that the UK's data is by definition some of the most reliable information in the world.    

There is good and bad news in their survival data.  The good news is that because it is so complete, it provides superb age related survival data.  The bad news is that the most recent survival numbers show an average 5 year life expectancy of just 37.1%, as compared to the USA's National Cancer Institutes 5 year survival of 44.5%.  One difference is that the UK data is for the years 2005 thru 2009, whereas the USA data is from 2004, but this would favor the UK data.    The 20% difference could be explained by several factors.  The USA has had earlier approval of some of the newer novel drugs, different demographics, or because our data only represents 30% of the population of the USA and the UK has a 100% sample.  However, what this does confirm is that the average survival rates of the leading myeloma specialists is 2 to 3 times better that these averages.  Which means the answer to the question; "How do you insure the longest life expectancy?" remains the same, and that is you need to have a skilled multiple myeloma specialist on your team.  

Now what does the data show about survival by age?  Below is the graph for the various age groups.  Like I mentioned previously, the average 5 year life expectancy is 37.1%.  I therefore believe you can make the case that if you are 65 years of age, your 5 year  life expectancy would be approximately 48.3%.  So you would be 1.2 times more likely to survive than the average myeloma patient.  A 55 year old myeloma patient would have a 5 year survival rate of approximately 55.8%, or be 1.4 times more likely to survive.  The last category, I will call the" less than 40 average" would be approximately 67.8%, or  2.0 times more likely to survive.  So to the younger patient of  around 40 years of age, you can expect to beat the averages by a fairly good margin.  For example if the current average by USA National Cancer Institute is 4 years and you have twice the life expectancy of the average, you could expect to live 8 years.  And if you are in the care of a skilled myeloma specialist whose average patient lives10 years or more, then you should hopefully outlive the cure.

As always, good luck and may God Bless your myeloma journey/ Gary Petersen [email protected] 

 

Figure 3.1: Myeloma (C90), Five-Year Relative Survival Rates by Age, England, 2005-2009
Picture
31 Comments
Susan Parker
12/13/2016 06:55:46 am

I found out I have Multiple Myeloma when I was 37. This coming Jan. I will celebrate 10 yrs remission. I pray I make it another 10

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Richie
6/1/2017 07:40:46 pm

This gives me hope, my girlfriend was diagnosed she is only 23yrs old.

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Theresa
6/2/2020 11:22:35 pm

Hallelujah! My brother is 42. He’s getting a stem cell transplant in the next week. I pray he gets at least 10 more years!

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Katy
10/12/2017 01:08:16 pm

2003 MGUS
2008 SMM 10% CELL IN BMB
2013 LARGE BCELL LYMPHOMA
2017 SMM 30% CELL'S FROM BMB
2017 PVNS IN KNEE]
HAS ANYONE HAD PVNS?

Reply
lawrence p. caragnano
9/20/2018 10:57:50 am

at age 77 mm diagnosis. I feel good and am being treated at Dana Farber cancer Institute in Boston. Good crew.

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Jayaprakash G
10/3/2020 11:06:25 pm

I am 71 now identified with mm
Your experience .pl share to my mail pl.

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Nancy Avery
10/22/2018 05:29:57 pm

I was diagnosed Feb 2007 at 62 yrs old. I received treatment at UAMS and have been in remission for 11 years. I am now 74 years old and sell Real Estate full time. I am also an artist and sell my art work. I feel very blessed and purposeful and enjoy an awesome life at St. Simons Island, GA

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abdul bahab
8/1/2019 03:08:38 am

can you email me on your treatment and story of success with myloma thanks

Reply
abdul bahab
8/31/2019 07:08:52 pm

like to know more about disease as i have it

Gary Petersen link
9/12/2019 05:19:21 pm

Abdul, At the bottom of the home page of www.myelomasurvival.com has a number of great links to improve your understanding of myeloma. Myeloma Crowd, the IMF and MMRF are my favorites. A good first read would be at the link: http://myelomasurvival.com/myeloma-blog/multiple-myeloma-2018-update-why-do-people-beat-the-average-myeloma-life-expectancy-prognosis-or-how-to-improve-your-multiple-myeloma-survival-rate Good luck and God Bless your myeloma journey/Gary

abdul bahab
10/12/2020 09:03:36 am

have my stem cell done in december doing fine so far having all my shots back and having bone stregetner . seeing my oconolgist every 3 months .

Andrew Fillo
3/25/2021 12:54:20 pm

Nancy,

I am 55. I was diagnosed 3 weeks ago. It has been traumatic and life changing as you well know. I am frightened but also hopeful. Bone marrow biopsy on April 2nd at Emory's Winship Cancer Center. Bone scan detects small tumors in my skull, right arm and vertebrae. I fractured 4 vertebrae from sneezing and coughing. Lost 3 inches in height. Thanks, Andy Atlanta GA

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Sylvia
9/28/2021 03:42:42 pm

Can you tell me what chemotherapy you were given and how often. I just started Dex/Bortezombib/cyclophosphamide once per week.
How are you currently doing?
I am 54 year old female

Nancy Avery
10/22/2018 05:41:45 pm

MM survivor for 11 years. I am 74 yrs. old and sell Real Estate full time.

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Tony Avila
6/8/2019 01:24:48 pm

My mother was diagnosed with stage 3 mm in 1994 when she was 58. She received autologous stem cell transplant immediately after. She is still alive 25 years later at 83 years old.

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Lorraine link
5/11/2020 02:41:07 pm

Hi. Did your mother have chemo or any other treatment besides the stem cell treatment? Thank you.

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Tony
6/5/2020 03:40:23 am

Sorry, I missed your question for a while. I also forgot about this previous comment of mine. Getting old! The only treatment she had was autologous stem cell transplant in 1994, and then she relapsed in 2007 for which she received Thalidomide for a few years and now that treatment has been stopped as it led to remission again. I believe she is just a rare outlier and her success is due to more than just early diagnosis, although no one in the medical field has offered an explanation concerning her longevity. Genetics, antioxidants, etc.?

Tony
6/5/2020 03:24:40 am

My mother was diagnosed with MM by the Moffet Cancer Center in Tampa, Florida in 1994. She was 58 at the time and Stage 3. 26 years later she is still living independently in her own home. I live 5 miles away from her and can run over anytime she needs help, but that is not often needed, she is very independent. I am an only child and my father passed away 30 years ago. I often joke with her that I have taken care of her longer than she took care of me as a child. I am now 65 and joke with her that she might outlive me. I am healthy but have Diabetes and often find it hard to eat like I should (as in very bland and tasteless). Having survived 26 years so far, there is probably more going on in her case than just being young at diagnosis. She may very well be an outlier, and if so, I hope I have inherited that from her!

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Albert Rodriguez
6/9/2020 10:30:43 am

Nancy Avery
What Cancer drug are you taking, Dose, and was a Stem Cell implant involved?
Thank you. Albert R.
I’m taking Revlimid 2.5 now.

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Charlene
7/1/2020 09:29:08 am

reading these comments.. i have hope.. i just found out I have Multiple Myeloma. My CT scan says my organs are all good. Having a bone marrow biopsy & PET scan next week. I'm 55 and before this, I was healthy with no underlying issues. I'm feeling so hopeful now.

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Charles Babcock
10/11/2020 06:16:31 pm

Hi I'm Charlie, just had my bone marrow biopsy last week. My doctor believes I have it. Purple horses certified in oncology hematology and I forget the third one 72 years. Born again Christian believer. Maybe I'll see Jesus sooner than I think. God bless you all and me also.

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Andrew s fillo
3/25/2021 01:05:43 pm

Charlene,

I am 55. I was diagnosed 3 weeks ago with mm. My kidneys and liver are ok. I have bone marrow biopsy next week. I'm a bit traumatized. I've broken 4 vertebrae in my spine b/c of tumors and osteoporosis. I lied. I Very traumatized.

Any feedback on how the process is going will be appreciated.

Andy

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Charlene Mottola
10/21/2021 05:06:54 am

Sorry took so long..I’m now on Revlimid 10mg. 10 months post SCT and I feel eh..achy most of the time. But I guess that’s better than some

Alan
9/27/2020 11:37:03 am

I was diagnosed with multi myeloma cancer in 2019 received bone marrow transplant at age 71 I am completing my first year of recovery I was very lucky I was treated at the Multiple myeloma clinic New York’ Citi which is part of New York Presbyterian Hospital Weil Cornell

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Lynette Hedderman
12/12/2020 03:10:18 am

I am 71 yrs & just been diagnosed with MGus with kappa light chains
& booked in to see a hematologist on the 20/1/2021 for more tests.
I live in Sydney,NSW.Australia.
I am so worried about my outcome,thinking I have cancer.

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Danny Mcmillan
2/25/2021 09:35:15 pm

I was diagnosed with early Stage 1 Light Chain MM in October 2019. Had Stem Cell Transplant in Oct 2020. Now in remission, no organ damage, currently 2.5% Plasma Involvement, Kappa LC at 5.5. Going on maintenance therapy now. I plan on living 25+ years. Medical technology WILL find a cure soon

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Brian
5/25/2021 12:19:45 pm

Not sure how often this page is read but thought I would share. My wife of 19 years at age 48 has been diagnosed with MM. She had bone and kidney biopsies in the last week and also PET scan. Just had call PET scan came back looking clear so that's good. Kidney DR believes caught in time that after treatment will be no problems with Kidneys. Have apt for 2nd opinion 2 days from now at Froedert in Milwaukee WI. Keeping faith as when I first started looking I feared the worse for her but now feeling more optimistic. If you have anything you think would help with our journey please let me know.
Oh - found out she had this by having a terrible reaction to the COVID shot and getting very sick. After 2 days bed riden took to urgent care where she was given fluids and blood test. The blood test came back with the high protein numbers that finally let to the MM diagnosis (approx 2 months latter). Kidney dr said without getting sick she would probably have been in bad shape in 6 months as currently she is healthy and feeling fine and would've never been checked for this.
Thanks.

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Janet Ngan
8/11/2021 10:32:12 am

My husband just diagnosed Iga myeloma today.
Anyone can share some experiences to me?

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Hortencia
2/17/2022 08:16:03 am

I was diagnosed with MM in 2011 and have undergo stem cell transplant. Currently, I am on maintenance treatment once per month. At first I did not understand what MM was and my outcome. Notice to all is follow your Hematology recommendation. As well as, there is a lot of education on the Leukemia and lymphoma society website.

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wlj
8/20/2022 12:36:32 am

It's August 20th. I'm 52 years and 8 months old. I was just diagnosed with MM. I'm not scared, mainly shocked and confused. The hospital is getting ready for more tests to determine the stage, but I'm almost positive it's stage III. I'm just here to read about others' experience and/or success stories. I don't feel very confident in what my prognosis will be. Any feedback or advice would be wel. Thank you

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Dave Charles
9/7/2022 11:21:30 am

Diagnosed in April; on RVD since May; scheduled for Stem Cell Transplant in October UPenn. Was doing long distance cycling, sailing, and in general overall great health. Rib pain sent me to my GP, who did a blood test and that's how I found out I had stage 2 MM. Went from feeling like a 45 year old to feeling like a 88 year old (I'm only 68). The treatments are gnarly and I just want to be able to do the things I used to do...Looking for any encouragement at all.

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    Author

    Gary R. Petersen
    [email protected]
    CLICK HERE for my myeloma journey

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