Hematology and Transplantation, Saint Louis Hospital, Paris, France.
Cellular Biology, Saint Louis Hospital, Paris, France; University of Paris, INSERM U1131, Paris, France.
Biol Blood Marrow Transplant. 2020 Jun;26(6):1160-1170. doi: 10.1016/j.bbmt.2020.02.019. Epub 2020 Feb 28.
BCR-ABL-negative myeloproliferative neoplasms (MPNs) in transformation have a dismal prognosis, and allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the sole curative therapeutic option. We retrospectively analyzed 53 molecularly annotated patients treated at Saint Louis Hospital, Paris, diagnosed with MPN in transformation between 2008 and 2018. The median patient age was 65 years, and the median interval between MPN diagnosis and MPN transformation was 46 months. The median overall survival (OS) of the entire cohort after transformation was 7.1 months. OS was better for patients treated with hypomethylating agents (HMAs) or with chemotherapy compared than for those treated by best supportive care or single-agent targeted therapy (median, 9.1 months versus 1.5 months; P < .001). Patients treated with chemotherapy more often achieved complete remission compared with those treated with HMAs (68% versus 29%; P = .02), and were more often candidates for transplantation (59% versus 14%; P = .02), but the median OS was similar in the 2 groups. We then compared the outcomes in transplant recipients and nonrecipients using the Mantel-Byar methodology and found that allo-HSCT did not improve survival. In multivariate analysis, independent factors in prognosis were performance status at transformation (P < .01), initial treatment with HMAs or chemotherapy (P = .02), and the ability to achieve complete remission during follow-up (P < .01). Our data demonstrate that the indication for allo-HSCT for high-risk MPN should be discussed before transformation, because transplantation rescues few patients after transformation.
BCR-ABL 阴性骨髓增殖性肿瘤(MPN)转化后的预后较差,异基因造血干细胞移植(allo-HSCT)被认为是唯一的治愈性治疗选择。我们回顾性分析了 2008 年至 2018 年间在巴黎圣路易医院诊断为 MPN 转化的 53 例分子注释患者。患者中位年龄为 65 岁,MPN 诊断与 MPN 转化之间的中位间隔为 46 个月。整个转化后队列的中位总生存期(OS)为 7.1 个月。与接受最佳支持治疗或单一靶向治疗的患者相比,接受低甲基化剂(HMAs)或化疗治疗的患者的 OS 更好(中位,9.1 个月比 1.5 个月;P<0.001)。与接受 HMAs 治疗的患者相比,接受化疗的患者更常达到完全缓解(68%比 29%;P=0.02),更常适合移植(59%比 14%;P=0.02),但两组的中位 OS 相似。然后,我们使用 Mantel-Byar 方法比较了移植患者和非移植患者的结果,发现 allo-HSCT 并不能改善生存。多变量分析显示,预后的独立因素是转化时的体能状态(P<0.01)、初始接受 HMAs 或化疗(P=0.02)以及随访期间达到完全缓解的能力(P<0.01)。我们的数据表明,对于高危 MPN,应在转化前讨论 allo-HSCT 的适应证,因为移植在转化后仅能挽救少数患者。