Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Acta Haematol. 2021;144(1):48-57. doi: 10.1159/000506146. Epub 2020 Mar 11.
Treatment options are limited for patients with advanced forms of myeloproliferative neoplasms (MPN) including blast-phase disease (MPN-BP). Decitabine has frequently been deployed but its efficacy and safety profile are not well described in this population. We retrospectively reviewed 42 patients treated with decitabine either alone or in combination with ruxolitinib at our institution: 16 with MPN-BP, 14 with MPN accelerated-phase (MPN-AP), and 12 with myelofibrosis with high-risk features (MF-HR). The median overall survival (OS) for the MPN-BP patients was 2.6 months, and for those who received ≥2 cycles of decitabine therapy, it was 6.7 months (3.8-29.8). MPN-BP patients with a poor performance status and who required hospitalization at the time of the initiation of decitabine had a dismal prognosis. After a median follow-up of 12.4 months for MPN-AP patients, and 38.7 months for MF-HR patients, the median OS was not reached for either cohort, with 1 and 2 patients alive at 60 months, respectively. The probability of spleen length reduction and transfusion independence within 12 months of initiating decitabine was 28.6 and 23.5%, respectively. The combination of decitabine and ruxolitinib appeared to improve overall survival versus single-agent decitabine (21 and 12.9 months, respectively). Decitabine, alone or in combination with ruxolitinib, appears to have clinical benefit for patients with advanced phases of MPN when initiated early in the disease course prior to the development of MPN-BP.
治疗选择有限,对于患有骨髓增生性肿瘤(MPN)晚期形式,包括爆发性疾病(MPN-BP)的患者。地西他滨经常被部署,但它的疗效和安全性在这一人群中描述得并不清楚。我们回顾性地审查了在我们机构接受地西他滨单独或与鲁索利替尼联合治疗的 42 名患者:16 名患有 MPN-BP,14 名患有 MPN 加速期(MPN-AP),12 名患有伴有高危特征的骨髓纤维化(MF-HR)。MPN-BP 患者的中位总生存期(OS)为 2.6 个月,接受≥2 个周期地西他滨治疗的患者中位 OS 为 6.7 个月(3.8-29.8)。在开始地西他滨治疗时,体能状态差且需要住院的 MPN-BP 患者预后不良。在 MPN-AP 患者的中位随访 12.4 个月和 MF-HR 患者的中位随访 38.7 个月后,两个队列的中位 OS 均未达到,分别有 1 名和 2 名患者在 60 个月时存活。在开始地西他滨治疗的 12 个月内,脾脏长度缩小和输血独立的概率分别为 28.6%和 23.5%。地西他滨联合鲁索利替尼似乎比单用地西他滨改善了总生存期(分别为 21 个月和 12.9 个月)。单独用地西他滨或与鲁索利替尼联合使用,在疾病早期(在发展为 MPN-BP 之前)开始时,对于患有 MPN 晚期的患者似乎具有临床获益。