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Pomalidomide-bortezomib-dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM.
Sunami, Kazutaka; Matsue, Kosei; Suzuki, Kenshi; Takezako, Naoki; Shinagawa, Atsushi; Sakurai, Sanae; Tamakoshi, Hiromi; Biyukov, Tsvetan; Peluso, Teresa; Richardson, Paul.
Afiliação
  • Sunami K; Department of Hematology, National Hospital Organization Okayama Medical Center, Okayama, Japan.
  • Matsue K; Department of Hematology, Kameda Medical Center, Chiba, Japan.
  • Suzuki K; Department of Hematology, Japanese Red Cross Medical Center, Tokyo, Japan.
  • Takezako N; Department of Hematology, National Hospital Organization Disaster Medical Center, Tokyo, Japan.
  • Shinagawa A; Department of Hemato-Oncology, Hitachi General Hospital, Ibaraki, Japan.
  • Sakurai S; Department of Clinical Research & Development Study, Celgene KK, a Bristol-Myers Squibb Company, Tokyo, Japan.
  • Tamakoshi H; Department of Clinical Research & Development Study, Celgene KK, a Bristol-Myers Squibb Company, Tokyo, Japan.
  • Biyukov T; Department of Clinical R&D Management, Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland.
  • Peluso T; Department of Clinical R&D Management, Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland.
  • Richardson P; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Cancer Sci ; 111(6): 2116-2122, 2020 Jun.
Article em En | MEDLINE | ID: mdl-32297407
ABSTRACT
In the phase 3 OPTIMISMM trial, pomalidomide, bortezomib and dexamethasone (PVd) significantly improved the progression-free survival (PFS) and the overall response rate (ORR) vs bortezomib and dexamethasone (Vd) in patients with relapsed or refractory multiple myeloma. All patients were previously treated with lenalidomide (70% refractory to lenalidomide) and had received one to three prior regimens. Here we report the first efficacy and safety analysis of PVd vs Vd in Japanese patients with relapsed or refractory multiple myeloma. Seventeen patients enrolled in the OPTIMISMM trial in Japan. With a median follow-up of 14.8 months, the median PFS was 17.6 months with PVd (n = 12) vs 4.4 months with Vd (n = 5), and the ORR was 100% vs 60.0%, respectively. The safety profile was as expected for PVd. Toxicities were managed with dose reductions and interruptions, and no patients discontinued PVd due to treatment-emergent adverse events. These results are consistent with those in the overall OPTIMISMM patient population and confirm the clinical benefit of PVd in Japanese patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Mieloma Múltiplo País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Mieloma Múltiplo País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão