Triplet vs doublet lenalidomide-containing regimens for the treatment of elderly patients with newly diagnosed multiple myeloma.

نویسندگان

  • Valeria Magarotto
  • Sara Bringhen
  • Massimo Offidani
  • Giulia Benevolo
  • Francesca Patriarca
  • Roberto Mina
  • Antonietta Pia Falcone
  • Lorenzo De Paoli
  • Giuseppe Pietrantuono
  • Silvia Gentili
  • Caterina Musolino
  • Nicola Giuliani
  • Annalisa Bernardini
  • Concetta Conticello
  • Stefano Pulini
  • Giovannino Ciccone
  • Vladimír Maisnar
  • Marina Ruggeri
  • Renato Zambello
  • Tommasina Guglielmelli
  • Antonio Ledda
  • Anna Marina Liberati
  • Vittorio Montefusco
  • Roman Hajek
  • Mario Boccadoro
  • Antonio Palumbo
چکیده

Lenalidomide-dexamethasone improved outcome in newly diagnosed elderly multiple myeloma patients. We randomly assigned 662 patients who were age ≥65 years or transplantation-ineligible to receive induction with melphalan-prednisone-lenalidomide (MPR) or cyclophosphamide-prednisone-lenalidomide (CPR) or lenalidomide plus low-dose dexamethasone (Rd). The primary end point was progression-free survival (PFS) in triplet (MPR and CPR) vs doublet (Rd) lenalidomide-containing regimens. After a median follow-up of 39 months, the median PFS was 22 months for the triplet combinations and 21 months for the doublet (P = .284). The median overall survival (OS) was not reached in either arms, and the 4-year OS was 67% for the triplet and 58% for the doublet arms (P = .709). By considering the 3 treatment arms separately, no difference in outcome was detected among MPR, CPR, and Rd. The most common grade ≥3 toxicity was neutropenia: 64% in MPR, 29% in CPR, and 25% in Rd patients (P < .0001). Grade ≥3 nonhematologic toxicities were similar among arms and were mainly infections (6.5% to 11%), constitutional (3.5% to 9.5%), and cardiac (4.5% to 6%), with no difference among the arms. In conclusion, in the overall population, the alkylator-containing triplets MPR and CPR were not superior to the alkylator-free doublet Rd, which was associated with lower toxicity. This study was registered at www.clinicaltrials.gov as #NCT01093196.

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عنوان ژورنال:
  • Blood

دوره 127 9  شماره 

صفحات  -

تاریخ انتشار 2016