Institute of Hematology, Davidoff Cancer Centre, Beilinson Hospital, Rabin Medical Centre, Petah-Tiqva, Israel; Sackler School of Medicine, Tel Aviv University, Ramat-Aviv, Israel.
Department of Hematology, Hadassah-Hebrew University Medical Centre, Jerusalem, Israel.
Clin Lymphoma Myeloma Leuk. 2018 Jul;18(7):e295-e301. doi: 10.1016/j.clml.2018.05.002. Epub 2018 May 7.
The strict recruitment criteria of patients for clinical trials often lead to reduced generalizability of the findings. We studied how ponatinib is used outside clinical trials in patients with chronic myeloid leukemia (CML).
The present retrospective study included all patients with a diagnosis of CML who had received ponatinib in 7 medical centers in Israel.
From 2011 to 2016, we identified 37 patients with CML who had received ponatinib, 21 in the chronic phase and 16 in the advanced phase. Only 9 patients (26%) harbored the T315I (threonine to isoleucine mutation at position 315) mutation. All patients had received ≥ 1 previous tyrosine kinase inhibitor. The median age in our cohort was 43 years (range, 9-82 years), significantly younger than expected for patients with relapsed or refractory CML and 20 years younger than the median age of patients who participated in the PACE (ponatinib Philadelphia-positive acute lymphoblastic leukemia and CML evaluation) trial. During a median follow-up of 14 months (range, 1-51 months), the overall response rate was 85%. Of 34 patients, 16 (47%) experienced at least a major molecular response. Of the 37 total patients, another 16 patients (43%) discontinued treatment because of disease progression (n = 6), vascular complications (n = 1), severe cytopenia (n = 2), or for other reasons (n = 7).
In real life, ponatinib is a "niche-drug" reserved for a unique population of exceptionally young patients with CML with or without the T315I mutation. In this highly selected group, very different from the PACE cohort, ponatinib achieved high overall response rates.
临床试验对患者的严格招募标准往往导致研究结果的普遍性降低。我们研究了在慢性髓性白血病(CML)患者中,波那替尼在临床试验之外的使用情况。
本回顾性研究纳入了在以色列 7 家医疗中心接受波那替尼治疗的所有 CML 患者。
2011 年至 2016 年,我们共发现 37 例接受波那替尼治疗的 CML 患者,慢性期 21 例,晚期 16 例。仅 9 例(26%)存在 T315I(第 315 位苏氨酸至异亮氨酸突变)突变。所有患者均接受过≥1 种酪氨酸激酶抑制剂治疗。本队列的中位年龄为 43 岁(范围 9-82 岁),明显低于复发或难治性 CML 患者的预期年龄,比参与 PACE(波那替尼费城阳性急性淋巴细胞白血病和 CML 评估)试验的患者中位年龄年轻 20 岁。中位随访 14 个月(范围 1-51 个月)期间,总体缓解率为 85%。34 例患者中,16 例(47%)至少达到主要分子缓解。37 例患者中,16 例(43%)因疾病进展(n=6)、血管并发症(n=1)、严重血细胞减少(n=2)或其他原因(n=7)而停止治疗。
在现实生活中,波那替尼是一种“利基药物”,仅适用于存在或不存在 T315I 突变的极少数年轻 CML 患者。在这个高度选择的群体中,与 PACE 队列非常不同,波那替尼取得了很高的总体缓解率。