A review of second primary malignancy in patients with relapsed or refractory multiple myeloma treated with lenalidomide. Academic Article uri icon

Overview

abstract

  • In a retrospective pooled analysis of 11 clinical trials of lenalidomide-based therapy for relapsed/refractory multiple myeloma (MM; N = 3846), the overall incidence rate (IR, events per 100 patient-years) of second primary malignancies (SPMs) was 3.62. IR of invasive (hematologic and solid tumor) SPMs was 2.08, consistent with the background incidence of developing cancer. In a separate analysis of pooled data from pivotal phase 3 trials of relapsed or refractory MM (N = 703), the overall IR of SPMs was 3.98 (95% confidence interval [CI], 2.51-6.31) with lenalidomide/dexamethasone and 1.38 (95% CI, 0.44-4.27) with placebo/dexamethasone; IRs of nonmelanoma skin cancers were 2.40 (95% CI, 1.33-4.33) and 0.91 (95% CI, 0.23-3.66), respectively; IRs of invasive SPMs were 1.71 (95% CI, 0.86-3.43) and 0.91 (95% CI, 0.23-3.66), respectively. The risk of SPMs must be taken into account before initiating lenalidomide treatment. In the context of the observed survival benefit in relapsed or refractory MM patients, the benefit/risk profile of lenalidomide/dexamethasone remains positive.

publication date

  • February 9, 2012

Research

keywords

  • Antineoplastic Agents
  • Multiple Myeloma
  • Neoplasms, Second Primary
  • Thalidomide

Identity

Scopus Document Identifier

  • 84858858229

Digital Object Identifier (DOI)

  • 10.1182/blood-2011-08-373514

PubMed ID

  • 22323483

Additional Document Info

volume

  • 119

issue

  • 12