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一线尼洛替尼治疗的临床疗效和安全性及基于 FRET 的药物敏感性试验的临床实用性评估。

Clinical efficacy and safety of first-line nilotinib therapy and evaluation of the clinical utility of the FRET-based drug sensitivity test.

机构信息

Department of Hematology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Blood Disorders Center, Aiiku Hospital, S4W25, Chuo-ku, Sapporo, 064-0804, Japan.

出版信息

Int J Hematol. 2019 Oct;110(4):482-489. doi: 10.1007/s12185-019-02696-w. Epub 2019 Jun 25.

Abstract

Nilotinib is widely used for primary treatment of patients with chronic myelogenous leukemia (CML). We previously reported that use of an FRET-based drug sensitivity test at diagnosis efficiently predicts the response to treatment with imatinib or dasatinib. Here, we conducted a phase-II study to evaluate the efficacy and safety of nilotinib treatment and identify useful biomarkers, including results of the FRET-based drug sensitivity test, for predicting treatment response. Data from 42 patients were used in the analysis. Major molecular response (MMR), MR4, and MR4.5 rates at 12 months were 64.3, 42.9, and 28.6%, respectively. Grade 3/4 non-hematologic adverse events occurred in 11 patients (26.2%). The dose intensity of nilotinib (> 76.44%) and halving time (HT, < 13.312 days) were identified as significant factors for MMR at 12 months. However, when we focused on patients whose dose intensity of nilotinib was > 76.44%, the FRET-based drug sensitivity test became a predictive factor of MR4 achievement at 12 months. Our study reconfirmed the efficacy and safety of nilotinib treatment in CML patients. Moreover, our results suggest that the FRET-based drug sensitivity test is an independent predictor for achievement of MR4 in patients treated with a sufficient dose intensity of nilotinib.

摘要

尼洛替尼被广泛用于慢性髓性白血病(CML)患者的一线治疗。我们之前曾报道,在诊断时使用基于荧光共振能量转移(FRET)的药物敏感性测试能够有效地预测伊马替尼或达沙替尼治疗的反应。在此,我们进行了一项 II 期研究,以评估尼洛替尼治疗的疗效和安全性,并确定有用的生物标志物,包括基于 FRET 的药物敏感性测试结果,以预测治疗反应。分析中使用了 42 名患者的数据。12 个月时的主要分子反应(MMR)、MR4 和 MR4.5 率分别为 64.3%、42.9%和 28.6%。11 名患者(26.2%)发生 3/4 级非血液学不良事件。尼洛替尼的剂量强度(>76.44%)和减半时间(HT,<13.312 天)被确定为 12 个月时 MMR 的显著因素。然而,当我们关注尼洛替尼剂量强度>76.44%的患者时,基于 FRET 的药物敏感性测试成为 12 个月时达到 MR4 的预测因素。我们的研究再次证实了尼洛替尼治疗 CML 患者的疗效和安全性。此外,我们的结果表明,对于接受足够尼洛替尼剂量强度治疗的患者,基于 FRET 的药物敏感性测试是达到 MR4 的独立预测因素。

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