AI Article Synopsis

  • Data on treating octogenarian patients with newly diagnosed multiple myeloma (NDMM) is limited, and this study examines a retrospective cohort of 74 such patients treated with bortezomib and dexamethasone.
  • The treatment involved initial induction therapy, followed by dose escalation with other drugs if patients didn't respond, leading to an overall response rate of 73%.
  • Despite the good response rate, median progression-free survival was 13.2 months, and overall survival was 26.9 months, with worse outcomes for patients with poor ECOG performance status, and there were significant early mortality rates during treatment.

Article Abstract

Data on octogenarian patients with MM are scarce, and optimal management remains controversial. We report a retrospective cohort of unselected octogenarian patients with NDMM treated with bortezomib dexamethasone (Vd). Seventy-four patients were treated with an initial doublet therapy (Vd regimen, 2−3 cycles, induction). A dose escalation with an adjunction of melphalan or cyclophosphamide was proposed for patients who had an insufficient response after induction and who could tolerate it. In responders, the treatment was continued until progression or a plateau response for 6 months (consolidation). The overall response rate was 73%. After a median follow-up of 31.4 months, median progression-free survival (PFS) and overall survival (OS) were 13.2 and 26.9 months, respectively. PFS and OS of patients with ECOG PS < 3 (25.4 and 54.9 months, respectively) were better in comparison to PFS and OS of patients with ECOG PS ≥ 3 (9.3 and 11.3 months, respectively). Thirteen patients (17.6%) died during induction. Twelve patients (16.2%) died during consolidation. In conclusion, a conservative therapeutic strategy based on Vd resulted in a good response rate. However, the survival remains poor in the population of patients with an ECOG PS ≥ 3, mainly because of early mortality not related to progressive disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564122PMC
http://dx.doi.org/10.3390/cancers14194741DOI Listing

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