Hematology, Department of Cellular Biotechnologies and Hematology, Policlinico Umberto 1, "Sapienza" University, Via Benevento 6, 00161, Rome, Italy.
S. Eugenio Hospital, Rome, Italy.
Ann Hematol. 2018 Sep;97(9):1577-1580. doi: 10.1007/s00277-018-3337-2. Epub 2018 Apr 19.
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.
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。