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

Author:

Rifkin Robert M1ORCID,Costello Caitlin L2,Birhiray Ruemu E3,Kambhampati Suman4,Richter Joshua5ORCID,Abonour Rafat6,Lee Hans C7,Stokes Michael8,Ren Kaili9,Stull Dawn Marie10,Cherepanov Dasha9,Bogard Kimberly10,Noga Stephen J10,Girnius Saulius11

Affiliation:

1. Rocky Mountain Cancer Centers/US Oncology Research, Denver, CO 80218, USA

2. Department of Medicine, Division of Blood & Marrow Transplantation, Moores Cancer Center, University of California San Diego, La Jolla, CA 92037, USA

3. Hematology Oncology of Indiana/American Oncology Network, Indianapolis, IN 46260, USA

4. Kansas City Veterans Affairs Medical Center, Kansas City, MO 64128, USA

5. Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA

6. Indiana University School of Medicine, Indianapolis, IN 46202, USA

7. M.D. Anderson Cancer Center, Houston, TX 77030, USA

8. Evidera, Data Analytics, St-Laurent, Quebec, H4T 1V6, Canada

9. Takeda Development Center Americas, Inc. (TDCA), Lexington, MA 02412, USA

10. Takeda Pharmaceuticals U.S.A., Inc., Lexington, MA 02421, USA

11. TriHealth Cancer Institute, Cincinnati, OH 45247, USA

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. Clinical Trial Registration: US MM-6: NCT03173092 ; INSIGHT MM: NCT02761187 ( ClinicalTrials.gov )

Funder

Takeda Development Center Americas, Inc. (TDCA), Lexington, MA

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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