Recently Diagnosed or Relapsed? Stop Looking For a Miracle Cure, and Use Evidence-Based Therapies To Enhance Your Treatment and Prolong Your Remission

Multiple Myeloma an incurable disease, but I have spent the last 25 years in remission using a blend of conventional oncology and evidence-based nutrition, supplementation, and lifestyle therapies from peer-reviewed studies that your oncologist probably hasn't told you about.

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Salvage Transplant in Myeloma?

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Does salvage transplant in myeloma help MM patients live longer? According to the research linked below, no, salvage ASCT shows no survival benefit.

To be clear, a salvage ASCT is not an FDA standard-of-care therapy ASCT that follows induction therapy for all NDMM patients. A salvage ASCT is not a tandem ASCT. A salvage ASCT is that ASCT that follows both an immediate ASCT, remission and then relapse.

I found the top finding below to be contradictory to all other findings regarding the benefit of salvage transplantation. The only difference I can determine is with the history of salvage ASCT findings, and the findings below are that “continuous dexamethasone/lenalidomide is a superior therapy for relapsed MM patients when compared to salvage ASCT.

I am a long-term MM survivor. Email me at David.PeopleBeatingCancer@gmail.com with questions about your MM.

Good luck,

David Emerson

  • MM Survivor
  • MM Cancer Coach
  • Director PeopleBeatingCancer

Myeloma: Does Salvage Transplant Show Benefit?

TOPLINE:

After a median follow-up of 99 months, salvage high-dose chemotherapy and autologous stem cell transplantation (sHDCT/ASCT) showed no survival benefit compared with continuous lenalidomide/dexamethasone in relapsed multiple myeloma. The absence of benefit was consistent across all subgroups, including patients with time to progression after frontline transplant beyond 48 months.

METHODOLOGY:

  • Researchers randomized 277 patients with relapsed and/or refractory multiple myeloma equally to receive either lenalidomide/dexamethasone reinduction followed by sHDCT/ASCT and lenalidomide maintenance or continuous lenalidomide/dexamethasone.
  • Participants received lenalidomide 25 mg on days 1-21 and dexamethasone 40 mg weekly in 4-week cycles, with the transplant arm receiving melphalan 200 mg/m2for sHDCT followed by lenalidomide maintenance at 10 mg daily.
  • Analysis included 94% of patients who had received frontline HDCT/ASCT, with 38% having received frontline tandem HDCT/ASCT, and 11% having previous lenalidomide exposure.

TAKEAWAY:

  • Median progression-free survival was 20.5 months (95% CI, 15.9-27.2) in the transplant arm vs 19.3 months (95% CI, 14.9-25.4) in the control arm (hazard ratio [HR], 0.98; 95% CI, 0.76-1.27; P = .9).
  • Overall survival showed no significant difference between arms, with median 67.1 months (95% CI, 59.2-85.4) vs 62.7 months (95% CI, 49.6-86.0) for the transplant arm vs the control arm (HR, 0.89; 95% CI, 0.66-1.20; P = .44).
  • Time to progression after frontline transplant did not predict benefit from salvage transplant, with no significant differences in survival even among patients with progression time beyond 48 months.
  • A 29% dropout rate was observed in the transplant arm before sHDCT/ASCT, primarily due to disease progression, adverse events, and withdrawal of consent.

Outcomes of Salvage Autologous Stem Cell Transplantation in Relapsed Multiple Myeloma: A Meta-Analysis

Background: Salvage autologous stem cell transplant (SAT)is an alternative treatment option for relapsed multiple myeloma patients that offers additional progression-free survival (PFS2) and overall survival (OS2) advantage over salvage chemotherapy. We conducted a meta-analysis to evaluate the outcomes of salvage transplant in patients with relapsed multiple myeloma after initial transplant…

Conclusion: SAT approach had favorable outcomes of achieving durable PFS and OS in relapsed myeloma patients. A Higher TRM was observed with salvage transplant than in upfront transplant. Prospective randomized trials are needed to define benefits of SAT in comparison with “best non-ASCT” therapy in patients with MM who relapse after primary therapy.”

 

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