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Isatuximab monotherapy in relapsed/refractory multiple myeloma: A Japanese, multicenter, phase 1/2, safety and efficacy study.
Sunami, Kazutaka; Suzuki, Kenshi; Ri, Masaki; Matsumoto, Morio; Shimazaki, Chihiro; Asaoku, Hideki; Shibayama, Hirohiko; Ishizawa, Kenichi; Takamatsu, Hiroyuki; Ikeda, Takashi; Maruyama, Dai; Kaneko, Hitomi; Uchiyama, Michihiro; Kiguchi, Toru; Iyama, Satoshi; Murakami, Hirokazu; Takahashi, Keishiro; Tada, Keisuke; Macé, Sandrine; Guillemin-Paveau, Hélène; Iida, Shinsuke.
Affiliation
  • Sunami K; Department of Hematology, National Hospital Organization, Okayama Medical Center, Okayama, Japan.
  • Suzuki K; Myeloma/Amyloidosis Center, Japanese Red Cross Medical Center, Tokyo, Japan.
  • Ri M; Department of Hematology and Oncology, Nagoya City University Institute of Medical and Pharmaceutical Sciences, Nagoya, Japan.
  • Matsumoto M; Department of Hematology, National Hospital Organization Shibukawa Medical Center, Shibukawa, Japan.
  • Shimazaki C; Department of Hematology, Japan Community Health care Organization Kyoto Kuramaguchi Medical Center, Kyoto, Japan.
  • Asaoku H; Department of Hematology, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Hiroshima, Japan.
  • Shibayama H; Department of Hematology and Oncology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Ishizawa K; Department of Third Internal Medicine, Division of Hematology and Cell Therapy, Yamagata University Faculty of Medicine, Yamagata, Japan.
  • Takamatsu H; Department of Hematology, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.
  • Ikeda T; Division of Hematology and Stem Cell Transplantation, Shizuoka Cancer Center, Shizuoka, Japan.
  • Maruyama D; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
  • Kaneko H; Department of Hematology, Japanese Red Cross Osaka Hospital, Osaka, Japan.
  • Uchiyama M; Department of Hematology, Japanese Red Cross Society Suwa Hospital, Suwa, Japan.
  • Kiguchi T; Department of Hematology, Chugoku Central Hospital, Fukuyama, Japan.
  • Iyama S; Department of Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Murakami H; Department of Laboratory Sciences, Gunma University Graduate School of Health Sciences, Maebashi, Japan.
  • Takahashi K; Research and Development, Sanofi K.K., Tokyo, Japan.
  • Tada K; Research and Development, Sanofi K.K., Tokyo, Japan.
  • Macé S; Research and Development, Sanofi, Vitry, France.
  • Guillemin-Paveau H; Research and Development, Sanofi, Vitry, France.
  • Iida S; Department of Hematology and Oncology, Nagoya City University Institute of Medical and Pharmaceutical Sciences, Nagoya, Japan.
Cancer Sci ; 111(12): 4526-4539, 2020 Dec.
Article in En | MEDLINE | ID: mdl-32975869
Isatuximab, an anti-CD38 monoclonal antibody, targets cells that strongly express CD38 including malignant plasma cells. This open-label, single-arm, multicenter, phase 1/2 trial investigated the tolerability/safety and efficacy of isatuximab monotherapy in Japanese patients with heavily pretreated, relapsed/refractory multiple myeloma (RRMM). In Phase 1, patients were sequentially assigned to receive isatuximab once weekly (QW) in cycle 1 (4 weeks) and every 2 weeks (Q2W) in subsequent cycles. Cohort 1 (n = 3) received 10 mg/kg QW/Q2W; cohort 2 (n = 5) received 20 mg/kg QW/Q2W. No dose-limiting toxicities occurred; the recommended dose for the single-arm phase 2 study (n = 28) was 20 mg/kg QW/Q2W. The overall safety profile was consistent with the current knowledge of isatuximab. The most common adverse events were infusion reactions (42.9%; 12/28); all were grade 1/2 and generally occurred during the first infusion. The overall response rate with 20 mg/kg QW/Q2W isatuximab was 36.4% (12/33); patients with high-risk cytogenetic abnormalities had comparable results. In phase 2, the median progression-free survival was 4.7 (95% confidence interval, 3.75 to not reached) months. Median overall survival was not reached. Isatuximab monotherapy was well tolerated and effective in patients with heavily pretreated RRMM including high-risk cytogenetic patients. This trial is registered at ClinicalTrials.gov as NCT02812706.
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Full text: 1 Database: MEDLINE Main subject: Antibodies, Monoclonal, Humanized / Multiple Myeloma / Antineoplastic Agents Type of study: Clinical_trials Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Cancer Sci Year: 2020 Type: Article Affiliation country: Japan

Full text: 1 Database: MEDLINE Main subject: Antibodies, Monoclonal, Humanized / Multiple Myeloma / Antineoplastic Agents Type of study: Clinical_trials Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Cancer Sci Year: 2020 Type: Article Affiliation country: Japan