A phase II study of ibrutinib in combination with ixazomib in patients with Waldenström macroglobulinaemia.
Ricardo D ParrondoNavnita DuttaBetsy R LaPlantJamie ElliottAndre FernandezAshley ZimmermanGina CiccoBing HanKeisha HeslopDustin ChapinTaimur SherVivek RoyAhsan RasheedSaurav DasAsher A Chanan-KhanAneel PaulusSikandar AilawadhiPublished in: British journal of haematology (2024)
This 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.
Keyphrases
- tyrosine kinase
- phase ii study
- newly diagnosed
- free survival
- open label
- epidermal growth factor receptor
- acute myeloid leukemia
- locally advanced
- randomized controlled trial
- acute lymphoblastic leukemia
- squamous cell carcinoma
- radiation therapy
- chronic lymphocytic leukemia
- combination therapy
- case report
- diffuse large b cell lymphoma
- rectal cancer