Sallan S E, Niemeyer C M, Billett A L, Lipton J M, Tarbell N J, Gelber R D, Murray C, Pittinger T P, Wolfe L C, Bast R C
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
J Clin Oncol. 1989 Nov;7(11):1594-601. doi: 10.1200/JCO.1989.7.11.1594.
Forty-four children with acute lymphoblastic leukemia (ALL) who had relapsed (N = 43) or had refractory disease (N = 1) were intensively treated with combination chemotherapy, had remission bone marrow (BM) harvested and purged in vitro with monoclonal antibodies specific for leukemia-associated antigens, underwent postharvest ablative chemotherapy and radiotherapy and subsequently were infused with their autologous marrow. Of the 44 patients treated between November 1980 and January 1988, 19 relapsed, 10 died of complications, and 15 remained in complete remission for a median of 28.5 months (range, 10+ to 94+). Event-free survival (EFS) (+/- SE) at 5 years after autologous transplantation was 29 +/- 8%. For the 26 patients whose initial remission was greater than 2 years, event-free survival was 51 +/- 10%. These results compare favorably with allogeneic transplantation and chemotherapy trials for patients with relapsed ALL, and provide an alternative transplantation option for children without histocompatible donors.
44例急性淋巴细胞白血病(ALL)复发(n = 43)或难治性疾病(n = 1)的儿童接受了强化联合化疗,采集缓解期骨髓(BM)并在体外使用针对白血病相关抗原的单克隆抗体进行净化,接受采集后清髓性化疗和放疗,随后输注自体骨髓。在1980年11月至1988年1月期间接受治疗的44例患者中,19例复发,10例死于并发症,15例持续完全缓解,中位缓解时间为28.5个月(范围为10 +至94 +)。自体移植后5年的无事件生存率(EFS)(±SE)为29 ± 8%。对于初始缓解期大于2年的26例患者,无事件生存率为51 ± 10%。这些结果与复发ALL患者的异基因移植和化疗试验相比具有优势,并为没有组织相容性供体的儿童提供了另一种移植选择。