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In-class transition from bortezomib-based therapy to IRd is an effective approach in newly diagnosed multiple myeloma

  • Robert M. Rifkin
  • , Caitlin L. Costello
  • , Ruemu E. Birhiray
  • , Suman Kambhampati
  • , Joshua Richter
  • , Rafat Abonour
  • , Hans C. Lee
  • , Michael Stokes
  • , Kaili Ren
  • , Dawn Marie Stull
  • , Dasha Cherepanov
  • , Kimberly Bogard
  • , Stephen J. Noga
  • , Saulius Girnius

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Aim: To compare the effectiveness of in-class transition to all-oral ixazomib-lenalidomide-dexamethasone (IRd) following parenteral bortezomib (V)-based induction versus continued V-based therapy in US oncology clinics. Patients & methods: Non-transplant eligible patients with newly diagnosed multiple myeloma (MM) receiving in-class transition to IRd (N = 100; US MM-6), or V-based therapy (N = 111; INSIGHT MM). Results: Following inverse probability of treatment weighting, overall response rate was 73.2% with IRd versus 57.5% with V-based therapy (p < 0.0001). Median duration of treatment was 10.8 versus 5.3 months (p < 0.0001). Overall, 18/24% of patients discontinued IRd/V-based therapy due to adverse events. Conclusion: IRd after V-based induction was associated with significantly improved overall response rate and duration of treatment than continued V-based combination therapy.

Original languageEnglish
Pages (from-to)131-143
Number of pages13
JournalFuture Oncology
Volume20
Issue number3
DOIs
StatePublished - 1 Jan 2024

Keywords

  • In-class transition
  • Ixazomib
  • oral therapy
  • proteasome inhibitor

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