Real-world long-term outcomes in multiple myeloma with VRD induction, Mel200-conditioned auto-HCT, and lenalidomide maintenance.
Mahmoud R GaballaJunsheng MaMark R TannerTaha Al-JuhaishiQaiser BashirSamer A SrourNeeraj Y SainiJeremy L RamdialYago NietoRegan MurphyKatayoun RezvaniGuillin TangHans C LeeKrina K PatelGregory P KaufmanElisabet E ManasanchMuhammad R UllahPartow KebriaeiSheeba K ThomasDonna M WeberRobert Z OrlowskiElizabeth J ShpallRichard E ChamplinMuzaffar H QazilbashPublished in: Leukemia & lymphoma (2021)
Standard-of-care for newly-diagnosed, autologous hematopoietic stem cell transplantation (auto-HCT)-eligible, multiple myeloma (MM) patients includes bortezomib, lenalidomide, and dexamethasone (VRD) induction followed by melphalan 200 mg/m2 (Mel200)-conditioned auto-HCT and lenalidomide maintenance. We completed a retrospective case series assessing outcomes of 187 MM patients who received this regimen at our institution. The 100-day non-relapse mortality incidence was zero. Before auto-HCT, 9.6 and 52.9% of patients achieved a complete response (CR) or ≥ very good partial response (VGPR), respectively. At day-100 post-transplant, 29.4 and 74.9% had achieved a CR/stringent-CR (sCR) or ≥ VGPR, respectively. At the last evaluation, 57.2% of patients had CR/sCR and 87.1% had ≥ VGPR. Median follow-up, progression-free survival (PFS), and overall survival (OS) were 63.2, 50, and 101.7 months, respectively. The 5-year PFS and OS were 43.1 and 79%. High-risk cytogenetics was associated with worse outcomes. This study illustrates that VRD induction, Mel200-conditioned auto-HCT, and lenalidomide maintenance are associated with good outcomes in MM.
Keyphrases
- newly diagnosed
- multiple myeloma
- end stage renal disease
- free survival
- ejection fraction
- chronic kidney disease
- high dose
- type diabetes
- cardiovascular disease
- stem cell transplantation
- metabolic syndrome
- cell cycle arrest
- stem cells
- signaling pathway
- skeletal muscle
- cell death
- patient reported outcomes
- palliative care
- adipose tissue
- cardiovascular events
- mesenchymal stem cells
- cell proliferation
- coronary artery disease
- patient reported
- platelet rich plasma