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Carfilzomib monotherapy in Japanese patients with relapsed or refractory multiple myeloma: A phase 1/2 study.

Authors :
Iida S
Watanabe T
Matsumoto M
Suzuki K
Sunami K
Ishida T
Ando K
Chou T
Ozaki S
Taniwaki M
Uike N
Shibayama H
Hatake K
Izutsu K
Ishikawa T
Shumiya Y
Tobinai K
Source :
Cancer science [Cancer Sci] 2019 Sep; Vol. 110 (9), pp. 2924-2932. Date of Electronic Publication: 2019 Aug 10.
Publication Year :
2019

Abstract

This multicenter, open-label phase 1/2 study evaluated single-agent carfilzomib in 50 heavily pretreated Japanese patients with relapsed/refractory multiple myeloma (median of five prior treatments). In phase 1, patients were dosed at three levels: 15, 20, or 20/27 mg/m <superscript>2</superscript> . Maximum tolerated dosage was not reached at the tolerability evaluation. Patients in phase 2 were treated with 20/27 mg/m <superscript>2</superscript> carfilzomib. Median duration of exposure to carfilzomib in the 20/27 mg/m <superscript>2</superscript> group at this final analysis was 4.7 months (range: 0.3-39.4). Overall response rate in the 20/27 mg/m <superscript>2</superscript> group, primary endpoint of the study, was 22.5% (n = 9) (95% confidence interval, 12.3-37.5) with 2.5% (n = 1) stringent complete response. Median progression-free survival and overall survival in the 20/27 mg/m <superscript>2</superscript> group were 5.1 months (95% CI, 2.8-13.6) and 22.9 months (95% CI, 14.1-not estimable), respectively. Frequently occurring grade ≥3 adverse events in the 20/27 mg/m <superscript>2</superscript> group included lymphopenia (72.5%), neutropenia (40.0%), and leukopenia (32.5%). Giving long-term carfilzomib monotherapy led to long-term overall survival for heavily pretreated multiple myeloma patients with a favorable safety profile. Carfilzomib monotherapy can be a good option for heavily pretreated multiple myeloma patients.<br /> (© 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.)

Details

Language :
English
ISSN :
1349-7006
Volume :
110
Issue :
9
Database :
MEDLINE
Journal :
Cancer science
Publication Type :
Academic Journal
Accession number :
31336012
Full Text :
https://doi.org/10.1111/cas.14139