Grosso Dolores, Gaballa Sameh, Alpdogan Onder, Carabasi Matthew, Filicko-O'Hara Joanne, Kasner Margaret, Martinez-Outschoorn Ubaldo, Wagner John L, O'Hara William, Rudolph Shannon, Chervoneva Inna, Colombe Beth, Farley Patricia Cornett, Flomenberg Phyllis, Pro Barbara, Sharma Manish, Shi Wenyin, Weiss Mark, Flomenberg Neal
Department of Medical Oncology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania.
Department of Medical Oncology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania.
Biol Blood Marrow Transplant. 2015 Apr;21(4):646-52. doi: 10.1016/j.bbmt.2014.12.019. Epub 2014 Dec 23.
Haploidentical hematopoietic stem cell transplantation (HSCT) is an attractive alternative donor option based on the rapid availability of an acceptable donor for most patients and decreased cost compared with costs of other alternative donor strategies. The safety of haploidentical HSCT has increased in recent years, making it ethically feasible to offer to patients with earlier stage disease. We developed a 2-step approach to haploidentical HSCT that separates the lymphoid and myeloid portions of the graft, allowing fixed T cell dosing to improve consistency in outcome comparisons. In the initial 2-step trial, the subset of patients without morphologic disease at HSCT had high rates of disease-free survival. To confirm these results, 28 additional patients without evidence of their disease were treated and are now 15 to 45 (median, 31) months past HSCT. To date, the 2-year cumulative incidence of nonrelapse mortality is 3.6%, with only 1 patient dying of nonrelapse causes, confirming the safety of this approach. Based on low regimen toxicity, the probabilities of disease-free and overall survival at 2 years are 74% and 77%, respectively, consistent with the findings in the initial trial and supporting the use of this approach in earlier stage patients lacking a matched related donor.
单倍体相合造血干细胞移植(HSCT)是一种颇具吸引力的替代供体选择,因为对于大多数患者而言,可快速获得合适的供体,且与其他替代供体策略相比成本降低。近年来,单倍体相合HSCT的安全性有所提高,使得为疾病处于早期阶段的患者提供该治疗在伦理上可行。我们开发了一种用于单倍体相合HSCT的两步法,该方法分离移植物的淋巴细胞和髓细胞部分,从而实现固定的T细胞剂量,以提高结果比较的一致性。在最初的两步试验中,HSCT时无形态学疾病的患者亚组具有较高的无病生存率。为了证实这些结果,另外28例无疾病证据的患者接受了治疗,目前已过HSCT 15至45个月(中位数为31个月)。迄今为止,非复发死亡率的2年累积发生率为3.6%,仅有1例患者死于非复发原因,证实了该方法的安全性。基于较低的方案毒性,2年时无病生存和总生存的概率分别为74%和77%,与最初试验的结果一致,并支持在缺乏匹配相关供体的早期患者中使用该方法。