eJHaem (Feb 2022)

Daratumumab combined with dexamethasone and lenalidomide or bortezomib in relapsed/refractory multiple myeloma (RRMM) patients: Report from the multiple myeloma GIMEMA Lazio group

  • Francesca Fazio,
  • Luca Franceschini,
  • Valeria Tomarchio,
  • Angela Rago,
  • Maria Grazia Garzia,
  • Luca Cupelli,
  • Velia Bongarzoni,
  • Alessandro Andriani,
  • Svitlana Gumenyuk,
  • Agostino Tafuri,
  • Agostina Siniscalchi,
  • Alfonso Piciocchi,
  • Paolo De Fabritiis,
  • Luca De Rosa,
  • Tommaso Caravita di Toritto,
  • Ombretta Annibali,
  • Maria Cantonetti,
  • Maria Teresa Petrucci

DOI
https://doi.org/10.1002/jha2.359
Journal volume & issue
Vol. 3, no. 1
pp. 121 – 128

Abstract

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Abstract The multiple myeloma (MM) treatment has changed over the last years due to the introduction of novel drugs. Despite improvements in the MM outcome, MM remains an incurable disease. Daratumumab is a human IgGK monoclonal antibody targeting CD38 with tumor activity associated with immunomodulatory mechanism. In combination with standard of care regimens, including bortezomib (Vd) or lenalidomide (Rd), daratumumab prolonged progression‐free survival (PFS) in patients (pts) with relapsed/refractory multiple myeloma (RRMM) and in new diagnosis MM. We report the data of the MM GIMEMA Lazio group in 171 heavily treated pts who received daratumumab, lenalidomide and dexamethasone (DRd) or daratumumab, velcade and dexamethasone (DVd). The overall response rate was 80%, and the overall survival (OS) and PFS were 84% and 77%, respectively. In addition, pts treated with DRd showed a better median PFS compared to pts treated with DVd, at 12 and 24 months, respectively. The most common hematologic treatment‐emergent adverse events (TAEs) were neutropenia, thrombocytopenia, and anemia. The most common nonhematologic TAEs were peripheral sensory neuropathy and infections. Our data confirmed that DRd or DVd therapy is effective and safe in RRMM pts, and our real‐life analysis could support the physicians regarding the choice of optimal therapy in this setting of pts.

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