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沙利度胺对日本骨髓瘤患者的维持治疗:一项多中心II期临床试验(COMET研究)。

Thalidomide maintenance therapy in Japanese myeloma patients: a multicenter, phase II clinical trial (COMET study).

作者信息

Murakami Hirokazu, Kasamatsu Tetsuhiro, Murakami Jun, Kiguchi Toru, Kanematsu Takeshi, Ogawa Daisuke, Takamatsu Hiroyuki, Handa Hiroshi, Ozaki Shuji, Miki Hirokazu, Takahashi Takeshi, Takeo Takaaki, Yamauchi Tatsuya, Morishita Takanobu, Kosugi Hiroshi, Shimizu Kazuyuki

机构信息

Department of Laboratory Sciences, Gunma University Graduate School of Health Sciences, Maebashi, Japan.

Department of Hematology, Toyama University Hospital, Toyama, Japan.

出版信息

Int J Hematol. 2019 Apr;109(4):409-417. doi: 10.1007/s12185-019-02607-z. Epub 2019 Jan 31.

Abstract

A prospective, multicenter, phase II study was performed to assess the efficacy and safety of thalidomide maintenance therapy at different doses in Japanese multiple myeloma (MM) patients. This study included 34 patients (median age, 74 years) who were previously treated with not more than three prior therapies and whose response status was evaluated as at least stable disease. They were randomized into Group A (no maintenance; 12 patients), Group B (50 mg thalidomide maintenance; 12 patients), and Group C (100 mg thalidomide maintenance; 10 patients), respectively. Thalidomide maintenance therapy resulted in improved depth of response in three cases (13.6%) and sustained response after induction therapy in eight cases (36.4%). Two-year progression-free survival (PFS) was 25.0%, 33.3%, and 77.8% in Groups A, B, and C, respectively, and was significantly higher in Group C than in Group A (p = 0.005). There was no difference in the incidence of hematological or non-hematological adverse events between Groups B and C. The current study demonstrates that maintenance with daily thalidomide at 100 mg, but not 50 mg, improved depth of response and prolonged PFS, and that this treatment was feasible for use in Japanese MM patients.

摘要

一项前瞻性、多中心、II期研究旨在评估沙利度胺维持治疗在不同剂量下对日本多发性骨髓瘤(MM)患者的疗效和安全性。该研究纳入了34例患者(中位年龄74岁),这些患者之前接受的治疗不超过三种,且反应状态评估为至少疾病稳定。他们被分别随机分为A组(无维持治疗;12例患者)、B组(沙利度胺50mg维持治疗;12例患者)和C组(沙利度胺100mg维持治疗;10例患者)。沙利度胺维持治疗使3例患者(13.6%)的反应深度得到改善,8例患者(36.4%)在诱导治疗后获得持续反应。A组、B组和C组的两年无进展生存期(PFS)分别为25.0%、33.3%和77.8%,C组显著高于A组(p = 0.005)。B组和C组血液学或非血液学不良事件的发生率没有差异。当前研究表明,100mg而非50mg的每日沙利度胺维持治疗可改善反应深度并延长PFS,且该治疗对日本MM患者可行。

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