Zaretsky Y, Rifkind J, Lockwood G, Tsang R, Kiss T, Hasegawa W, Fyles G, Tejpar I, Loach D, Minden M, Messner H, Lipton J H
Department of Medical Oncology and Hematology, University of Toronto Allogeneic Blood and Marrow Transplant Program, Toronto, Ontario, Canada.
Bone Marrow Transplant. 2007 Sep;40(5):423-30. doi: 10.1038/sj.bmt.1705755. Epub 2007 Jul 2.
We evaluated long-term toxicities and outcomes in 96 patients with chronic phase chronic myeloid leukemia treated with a single bone marrow allograft regimen. Conditioning was cytosine arabinoside, cyclophosphamide (120 mg/kg) and single fraction total body irradiation (500 cGy). Median follow-up was 12.8 years (0.4-19.9 years). Graft failure occurred in one patient, nonfatal veno-occlusive disease in 13 patients (14%). Overall incidences of acute (a) and chronic (c) graft-vs-host disease (GVHD) were 77 and 63%. The 100-day and 1-year transplant-related mortality (TRM) were 1 and 9.2%, respectively, with no change through 5 years. Five- and 10-year event-free survival rates were 56 and 49%, overall survival (OS) rates 72 and 70%, respectively. Forty patients have relapsed: 8 cytogenetic (20%), 10 hematologic (25%) and 22 molecular (55%). Most have been salvaged with donor-leukocyte infusion, second transplants and/or imatinib therapy. Survival was worse for patients transplanted >2 years from diagnosis (10-year OS 56 vs 78%, P=0.01), for patients over 50 years old (10-year OS 44 vs 75%, P=0.05) and for patients without cGVHD (10-year OS 53 vs 86%, P<0.001). This regimen resulted in successful engraftment, low risk of TRM and long-term survival. In an era when imatinib is first line therapy, this regimen offers a potentially low-toxicity, highly successful alternative in the event of poor imatinib response.
我们评估了96例接受单一骨髓同种异体移植方案治疗的慢性期慢性髓性白血病患者的长期毒性和预后。预处理方案为阿糖胞苷、环磷酰胺(120mg/kg)及单次全身照射(500cGy)。中位随访时间为12.8年(0.4 - 19.9年)。1例患者发生移植失败,13例患者(14%)发生非致命性静脉闭塞性疾病。急性(a)和慢性(c)移植物抗宿主病(GVHD)的总体发生率分别为77%和63%。100天和1年的移植相关死亡率(TRM)分别为1%和9.2%,5年内无变化。5年和10年无事件生存率分别为56%和49%,总生存率(OS)分别为72%和70%。40例患者复发:8例为细胞遗传学复发(20%),10例为血液学复发(25%),22例为分子学复发(55%)。大多数患者通过供者淋巴细胞输注、二次移植和/或伊马替尼治疗得到挽救。诊断后超过2年接受移植的患者生存率较差(10年OS为56% vs 78%,P = 0.01),50岁以上患者(10年OS为44% vs 75%,P = 0.05)以及无慢性GVHD的患者(10年OS为53% vs 86%,P < 0.001)。该方案导致成功植入、TRM风险低且长期生存。在伊马替尼作为一线治疗的时代,对于伊马替尼反应不佳的情况,该方案提供了一种潜在低毒性、高度成功的替代方案。