PofoliaShared via Pofolia

New England Journal of Medicine· 2017Q1

Lenalidomide, Bortezomib, and Dexamethasone with Transplantation for Myeloma

Michel Attal, Valérie Lauwers‐Cancès, Cyrille Hulin, Xavier Leleu et al.

Short summary

High-dose chemotherapy plus stem-cell transplantation combined with lenalidomide, bortezomib, and dexamethasone (RVD) therapy resulted in significantly longer progression-free survival (50 months vs. 36 months) compared to RVD therapy alone in newly diagnosed multiple myeloma patients.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Stem-cell transplantation plus RVD therapy extended median progression-free survival to 50 months vs. 36 months for RVD alone (hazard ratio for progression/death, 0.65; P<0.001).
  • Complete response rates were higher with transplantation (59% vs. 48%), as was minimal residual disease negativity (79% vs. 65%).
  • Overall survival at 4 years was similar between the transplantation group (81%) and the RVD-alone group (82%).
  • The transplantation group had significantly higher rates of grade 3 or 4 neutropenia (92% vs. 47%) and gastrointestinal disorders (28% vs. 7%).

AI-generated from the title and abstract; the full text is not read.

Abstract

BACKGROUND: High-dose chemotherapy plus autologous stem-cell transplantation has been the standard treatment for newly diagnosed multiple myeloma in adults up to 65 years of age. However, promising data on the use of combination therapy with lenalidomide, bortezomib, and dexamethasone (RVD) in this population have raised questions about the role and timing of transplantation. METHODS: We randomly assigned 700 patients with multiple myeloma to receive induction therapy with three cycles of RVD and then consolidation therapy with either five additional cycles of RVD (350 patients) or high-dose melphalan plus stem-cell transplantation followed by two additional cycles of RVD (350 patients). Patients in both groups received maintenance therapy with lenalidomide for 1 year. The primary end point was progression-free survival. RESULTS: Median progression-free survival was significantly longer in the group that underwent transplantation than in the group that received RVD alone (50 months vs. 36 months; adjusted hazard ratio for disease progression or death, 0.65; P<0.001). This benefit was observed across all patient subgroups, including those stratified according to International Staging System stage and cytogenetic risk. The percentage of patients with a complete response was higher in the transplantation group than in the RVD-alone group (59% vs. 48%, P=0.03), as was the percentage of patients in whom minimal residual disease was not detected (79% vs. 65%, P<0.001). Overall survival at 4 years did not differ significantly between the transplantation group and the RVD-alone group (81% and 82%, respectively). The rate of grade 3 or 4 neutropenia was significantly higher in the transplantation group than in the RVD-alone group (92% vs. 47%), as were the rates of grade 3 or 4 gastrointestinal disorders (28% vs. 7%) and infections (20% vs. 9%). No significant between-group differences were observed in the rates of treatment-related deaths, second primary cancers, thromboembolic events, and peripheral neuropathy. CONCLUSIONS: Among adults with multiple myeloma, RVD therapy plus transplantation was associated with significantly longer progression-free survival than RVD therapy alone, but overall survival did not differ significantly between the two approaches. (Supported by Celgene and others; IFM 2009 Study ClinicalTrials.gov number, NCT01191060 .).

The authors' abstract, as published at the source. New England Journal of Medicine, 2017 · DOI ↗

TakeawaysPremium
Ask the paperFree account

Continue with a free account

Ask the paper: 3 free questions a day about this paper; save it, get its citation, new summaries every day for your field. Takeaways are Premium.

Continue free on the web

Sign in with Google or Apple; no card needed. You come back to this paper.

On your phone:

Field: Hematology

HematologyMedicine