A phase II study of ibrutinib in combination with ixazomib in patients with Waldenström macroglobulinaemia

Author:

Parrondo Ricardo D.1ORCID,Dutta Navnita2,LaPlant Betsy R.3,Elliott Jamie1,Fernandez Andre1,Zimmerman Ashley1,Cicco Gina2,Han Bing2,Heslop Keisha1,Chapin Dustin1,Sher Taimur1,Roy Vivek1,Rasheed Ahsan1,Das Saurav1ORCID,Chanan‐Khan Asher A.12ORCID,Paulus Aneel2,Ailawadhi Sikander12ORCID

Affiliation:

1. Mayo Clinic Cancer Center Jacksonville Florida USA

2. Department of Cancer Biology Mayo Clinic Jacksonville Florida USA

3. Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA

Abstract

SummaryThis phase II study evaluated time‐limited (24 cycles) treatment with ibrutinib and ixazomib in newly diagnosed (NDWM; n = 9) and relapsed/refractory (RRWM; n = 12) Waldenström macroglobulinaemia (WM). The overall response rate (ORR) was 76.2% (n = 16) in 21 evaluable patients with no patient achieving a complete response (CR). The median duration of treatment was 15.6 months, and after a median follow‐up time of 25.7 months, the median progression‐free survival (PFS) was 22.9 months. While the primary end‐point was not met (CR rate at any time) and 28.5% discontinued treatment due to toxicity, ibrutinib plus ixazomib led to a clinically meaningful ORR and PFS. Combined Bruton's tyrosine kinase (BTK) and proteasome inhibition merits further evaluation in WM.

Funder

Takeda Oncology

Publisher

Wiley

Subject

Hematology

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