Volume 83, Issue 11 pp. 835-839
Research Article
Free Access

Multicenter prospective trial evaluating the tolerability of imatinib for Japanese patients with chronic myelogenous leukemia in the chronic phase: Does body weight matter?

Yoshinobu Kanda

Corresponding Author

Yoshinobu Kanda

Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan

Division of Hematology, Saitama Medical Center, Jichi Medical University, 1-847 Amanuma, Omiya, Saitama-city, Saitama 330-8503, JapanSearch for more papers by this author
Shinichiro Okamoto

Shinichiro Okamoto

Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Tetsuzo Tauchi

Tetsuzo Tauchi

First Department of Internal Medicine, Tokyo Medical University, Tokyo, Japan

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Masahiro Kizaki

Masahiro Kizaki

Division of Hematology, Department of Internal Medicine, Saitama Medical Center, Saitama Medical University, Saitama, Japan

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Koiti Inokuchi

Koiti Inokuchi

Department of Hematology, Nippon Medical School, Tokyo, Japan

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Mariko Yabe

Mariko Yabe

Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Kenji Yokoyama

Kenji Yokoyama

Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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Yoshikazu Ito

Yoshikazu Ito

First Department of Internal Medicine, Tokyo Medical University, Tokyo, Japan

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Yukihiko Kimura

Yukihiko Kimura

First Department of Internal Medicine, Tokyo Medical University, Tokyo, Japan

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Masaaki Higashihara

Masaaki Higashihara

Department of Hematology, Kitasato University School of Medicine, Kanagawa, Japan

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Masami Bessho

Masami Bessho

Division of Hematology, Department of Internal Medicine, Saitama Medical University, Saitama, Japan

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Kiyoshi Ando

Kiyoshi Ando

Division of Hematology and Oncology, Department of Internal Medicine, Tokai University School of Medicine, Kanagawa, Japan

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Shigeru Chiba

Shigeru Chiba

Department of Cell Therapy and Transplantation Medicine, University of Tokyo, Tokyo, Japan

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Mineo Kurokawa

Mineo Kurokawa

Department of Hematology and Oncology, University of Tokyo, Tokyo, Japan

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Kazuo Oshimi

Kazuo Oshimi

Division of Hematology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan

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Kazuo Dan

Kazuo Dan

Department of Hematology, Nippon Medical School, Tokyo, Japan

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Kazuma Ohyashiki

Kazuma Ohyashiki

First Department of Internal Medicine, Tokyo Medical University, Tokyo, Japan

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Yasuo Ikeda

Yasuo Ikeda

Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

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First published: 21 August 2008
Citations: 13

Conflict of Interest: Nothing to report.

Abstract

Imatinib at a daily dose of 400 mg is the standard treatment for chronic myelogenous leukemia in the chronic phase. However, the feasibility of this dose for small Japanese adults has not been clarified. We prospectively investigated the toxicity and efficacy of this dose in adult Japanese patients. Among the 89 evaluable patients with a median body weight of 62.8 kg, imatinib therapy was held in 40 subjects (45%), due to Grade 3–4 toxicities in 30 patients (75%) and Grade 2 toxicities at the discretion of the attending physician in 10 patients (25%). However, treatment was resumed and the dose was gradually increased until 62 of the 89 patients tolerated a maintenance dose of 400 mg. Older age and lower body weight were significant independent risk factors for discontinuation of imatinib. After a median follow-up period of 31 months, 84 patients were alive without progression. The complete cytogenetic response rate was 60 and 90% at 6 months and 1 year after starting imatinib, respectively. Older patients and those with a lower body weight were less likely to achieve a complete cytogenetic response. These findings suggest that the body weight has a significant influence on the toxicity and efficacy of imatinib in patients with a small body size, although dose reduction in proportion to weight may result in an inadequate response to imatinib. Am. J. Hematol., 2008. © 2008 Wiley-Liss, Inc.

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