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真实世界实践中,ponatinib 作为二线治疗用于慢性期慢性髓性白血病患者。

Ponatinib as second-line treatment in chronic phase chronic myeloid leukemia patients in real-life practice.

机构信息

Hematology, Department of Cellular Biotechnologies and Hematology, Policlinico Umberto 1, "Sapienza" University, Via Benevento 6, 00161, Rome, Italy.

S. Eugenio Hospital, Rome, Italy.

出版信息

Ann Hematol. 2018 Sep;97(9):1577-1580. doi: 10.1007/s00277-018-3337-2. Epub 2018 Apr 19.

DOI:10.1007/s00277-018-3337-2
PMID:29675611
Abstract

Scarce information is available on the use of ponatinib as second-line treatment in chronic phase chronic myeloid leukemia (CP-CML) patients resistant and/or intolerant to prior tyrosine kinase inhibitor (TKI) therapy. We collected data from 29 CML patients, with a median age of 54 years (range 32-72). Eleven patients had received dasatinib, 15 patients received nilotinib, and 3 patients received imatinib as first-line treatment. Forty-five percent of patients started ponatinib for secondary resistance, 38% for primary resistance, 7% for severe intolerance associated to a molecular warning, 7% due to the presence of a T315I mutation, and 3% for severe intolerance. Ponatinib was started at a dose of 45 mg in 60% of patients, 30 mg in 38%, and 15 mg in 2% of patients. Overall, at a median follow-up of 12 months, 85% of treated patients improved the level of response as compared to baseline, with 10 patients achieving a deep molecular response (MR4-4.5). No thrombotic events were recorded. The dose was reduced during treatment in 2 patients due to intolerance and in 8 patients in order to reduce the cardiovascular risk. Ponatinib seems a valid second-line treatment option for chronic phase CML, in particular for patients who failed a front-line second-generation TKI due to BCR-ABL-independent mechanisms of resistance.

摘要

关于既往对酪氨酸激酶抑制剂(TKI)治疗耐药和/或不耐受的慢性期慢性髓性白血病(CP-CML)患者使用波那替尼作为二线治疗的信息有限。我们从 29 例 CML 患者中收集了数据,中位年龄为 54 岁(范围 32-72)。11 例患者接受过达沙替尼治疗,15 例患者接受过尼洛替尼治疗,3 例患者接受过伊马替尼作为一线治疗。45%的患者因继发耐药而开始使用波那替尼,38%的患者因原发耐药而开始使用波那替尼,7%的患者因严重不耐受和分子预警而开始使用波那替尼,7%的患者因存在 T315I 突变而开始使用波那替尼,3%的患者因严重不耐受而开始使用波那替尼。60%的患者起始剂量为 45mg,38%的患者起始剂量为 30mg,2%的患者起始剂量为 15mg。总体而言,在中位随访 12 个月时,与基线相比,85%的治疗患者的缓解水平得到了改善,其中 10 例患者达到了深度分子缓解(MR4-4.5)。未记录到血栓事件。由于不耐受,有 2 名患者在治疗过程中减少了剂量,有 8 名患者为了降低心血管风险而减少了剂量。波那替尼似乎是慢性期 CML 的一种有效的二线治疗选择,特别是对于因 BCR-ABL 独立耐药机制而在前一线第二代 TKI 治疗失败的患者。

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