Black multiple myeloma patients can have better survival rates compared to their white patient counterparts when treated equally, according to new research from the Medical College of Wisconsin.
Using the SEER Medicare database with data from 1999 and 2017, the researchers reviewed differences in survival between non-Hispanic Black patients (3319) and non-Hispanic white patients (20,831) with multiple myeloma. They then broke Black patients into four subgroups areas based on: 1) demographics 2) socioeconomic status 3) presentation factors (socioeconomic factors plus comorbidities) and treatment factors (presentation variables plus myeloma therapies received.)
Black patients were younger on average (76.1 vs 77.1) and more likely to be female (60% vs. 48%) and to be unmarried at diagnosis (42% vs. 25.2%). Black patients also had lower socioeconomic status but had more comorbidities (pre-existing health conditions).
Treatments that were included in the data included: chemotherapy (melphalan, doxorubicin, vincristine, cyclophosphamide, etoposide, bendamustine, and carmustine), proteasome inhibitors (bortezomib, carfilzomib and ixazomib), immunomodulators (thalidomide, lenalidomide and pomalidomide) and stem cell transplant. Newer drugs like daratumumab, isatuximab and other immunotherapies were not included.
When it came to treatments, Black patients were less likely to use the following treatments (when matching for socioeconomic status and comorbidities):
Key findings of the study included:
This means that if Black patients have the same socioeconomic factors, similar pre-existing health conditions and the same treatment, they will live longer than whites.
As a myeloma patient community, it is imperative that we ensure that all patients know about their treatment options available at every stage of disease. There is no reason that all patients should not receive equal care and their best possible outcomes. With equal care, Black patients could live longer, better lives.
about the author
Jennifer Ahlstrom
Myeloma survivor, patient advocate, wife, mom of 6. Believer that patients can help accelerate a cure by weighing in and participating in clinical research. Founder of HealthTree Foundation (formerly Myeloma Crowd).
Subscribe to the weekly "HealthTree Community for Myeloma Newsletter" for Myeloma news, life with Myeloma stories, Myeloma clinical trials, Myeloma 101 articles and events with Myeloma experts.