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New England Journal of Medicine· 2012Q1

Lenalidomide after Stem-Cell Transplantation for Multiple Myeloma

Philip L. McCarthy, Kouros Owzar, Craig C. Hofmeister, David D. Hurd et al.

Short summary

Lenalidomide maintenance therapy after autologous stem-cell transplantation significantly extended the median time to disease progression (46 vs. 27 months) and improved overall survival in multiple myeloma patients, despite increased toxicity and second cancers.

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Key points

  • Lenalidomide maintenance therapy extended median progression-free survival to 46 months vs. 27 months for placebo (P<0.001).
  • Overall survival was improved, with 37% of lenalidomide patients experiencing progression or death vs. 58% for placebo at 34 months median follow-up.
  • Lenalidomide use was associated with increased grade 3/4 hematologic and nonhematologic adverse events.
  • Second primary cancers occurred in 8% of lenalidomide patients vs. 3% of placebo patients.

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

Abstract

BACKGROUND: Data are lacking on whether lenalidomide maintenance therapy prolongs the time to disease progression after autologous hematopoietic stem-cell transplantation in patients with multiple myeloma. METHODS: Between April 2005 and July 2009, we randomly assigned 460 patients who were younger than 71 years of age and had stable disease or a marginal, partial, or complete response 100 days after undergoing stem-cell transplantation to lenalidomide or placebo, which was administered until disease progression. The starting dose of lenalidomide was 10 mg per day (range, 5 to 15). RESULTS: The study-drug assignments were unblinded in 2009, when a planned interim analysis showed a significantly longer time to disease progression in the lenalidomide group. At unblinding, 20% of patients who received lenalidomide and 44% of patients who received placebo had progressive disease or had died (P<0.001); of the remaining 128 patients who received placebo and who did not have progressive disease, 86 crossed over to lenalidomide. At a median follow-up of 34 months, 86 of 231 patients who received lenalidomide (37%) and 132 of 229 patients who received placebo (58%) had disease progression or had died. The median time to progression was 46 months in the lenalidomide group and 27 months in the placebo group (P<0.001). A total of 35 patients who received lenalidomide (15%) and 53 patients who received placebo (23%) died (P=0.03). More grade 3 or 4 hematologic adverse events and grade 3 nonhematologic adverse events occurred in patients who received lenalidomide (P<0.001 for both comparisons). Second primary cancers occurred in 18 patients who received lenalidomide (8%) and 6 patients who received placebo (3%). CONCLUSIONS: Lenalidomide maintenance therapy, initiated at day 100 after hematopoietic stem-cell transplantation, was associated with more toxicity and second cancers but a significantly longer time to disease progression and significantly improved overall survival among patients with myeloma. (Funded by the National Cancer Institute; ClinicalTrials.gov number, NCT00114101.).

The authors' abstract, as published at the source. New England Journal of Medicine, 2012 · DOI ↗

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Field: Hematology

HematologyMedicine