4.5 Article

Two-year outcomes of tirabrutinib monotherapy in Waldenstrom's macroglobulinemia

Journal

CANCER SCIENCE
Volume 113, Issue 6, Pages 2085-2096

Publisher

WILEY
DOI: 10.1111/cas.15344

Keywords

Bruton's tyrosine kinase inhibitor; Japanese; phase II; two-year follow-up; Waldenstrom's macroglobulinemia

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Funding

  1. Ono Pharmaceutical

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The phase II study of tirabrutinib monotherapy showed promising efficacy and acceptable safety profile for the treatment of Waldenstrom's macroglobulinemia. Most disease-related symptoms improved and patient-reported quality of life was mostly maintained.
The phase II study of tirabrutinib monotherapy at a daily dose of 480 mg under fasting conditions for treatment-naive and relapsed/refractory Waldenstrom's macroglobulinemia (ONO-4059-05 study) demonstrated a promising efficacy and tolerable safety profile. We conducted an unplanned analysis with a median follow-up of 24.8 months to update the efficacy and safety results and to report patient-reported quality of life. Of 27 enrolled patients, 22 patients continued receiving the study drug. The major response assessed by an independent review committee was observed in 25 patients (93%), including one and five patients who newly achieved complete response and very good partial response, respectively, after the primary analysis. The progression-free and overall survival rates at 24 months were 92.6% and 100%, respectively. Serum IgM levels in all patients except one declined and were maintained at low levels, although transient increases occurred after temporal interruption of the study drug. The disease-related symptoms including recurrent fever and hyperviscosity mostly disappeared. Health-related quality of life, assessed by cancer-specific questionnaires, was mostly maintained. Grade 3-4 neutropenia, lymphopenia, and leukopenia were newly recognized in three, two, and one patient, respectively. Grade 3 treatment-related hypertriglyceridemia was also recognized. Nine patients experienced grade 1-2 bleeding events (33%), one patient experienced grade 2 treatment-related atrial fibrillation, and one patient experienced grade 1 treatment-related hypertension. Treatment-related skin adverse events were observed in 14 patients (52%). Taken together, tirabrutinib has durable efficacy with an acceptable safety profile for treatment-naive and refractory/relapsed Waldenstrom's macroglobulinemia.

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