Parsons S K, Castellino S M, Lehmann L E, Eickhoff C E, Tarbell N J, Sallan S E, Weinstein H J, Billett A L
Division of Hematology@Oncology, Children's Hospital, Boston, MA, USA
Bone Marrow Transplant. 1996 May;17(5):763-8.
The therapy of choice for relapsed childhood acute lymphoblastic leukemia is controversial. We retrospectively compared the outcome of 57 patients who received autologous bone marrow transplantation (BMT) with 17 patients who underwent allogeneic BMT for B cell lineage acute lymphoblastic leukemia after at least one marrow relapse. The allogeneic BMT cohort included only those who would also have been eligible for autologous BMT had they not had a matched sibling donor. Specifically, patients who were not in complete remission, those with T cell positive leukemia, t(9;22) or those with only an extramedullary relapse were excluded from both groups. Conditioning regimens included total body irradiation and chemotherapy. Age, white blood count at diagnosis, and duration of first and longest complete remissions were comparable for the two groups. The median follow-up of the event-free survivors was 4.8 years for those who received an autologous BMT (n = 26) and 4.6 years for those who received an allogeneic BMT (n = 8). The relapse rate was higher in the autologous BMT group and the incidence of non-leukemic deaths higher in the allogeneic BMT group. Event-free survival at 3 years was comparable for the two groups (47% +/- 7 vs 53% +/- 12, autologous vs allogeneic, respectively; P = 0.77). Based upon these findings, we concluded that the outcome for autologous BMT was equivalent to allogeneic BMT for relapsed childhood B cell lineage acute lymphoblastic leukemia in selected clinical situations.
复发性儿童急性淋巴细胞白血病的首选治疗方法存在争议。我们回顾性比较了57例接受自体骨髓移植(BMT)的患者与17例在至少一次骨髓复发后接受异基因BMT治疗B细胞系急性淋巴细胞白血病的患者的预后。异基因BMT队列仅包括那些如果没有匹配的同胞供体也有资格接受自体BMT的患者。具体而言,两组均排除未完全缓解的患者、T细胞阳性白血病患者、t(9;22)患者或仅发生髓外复发的患者。预处理方案包括全身照射和化疗。两组患者的年龄、诊断时的白细胞计数以及首次和最长完全缓解的持续时间具有可比性。接受自体BMT的无事件生存者的中位随访时间为4.8年(n = 26),接受异基因BMT的为4.6年(n = 8)。自体BMT组的复发率较高,异基因BMT组的非白血病死亡率较高。两组的3年无事件生存率相当(自体组和异基因组分别为47%±7和53%±12;P = 0.77)。基于这些发现,我们得出结论,在特定临床情况下,复发性儿童B细胞系急性淋巴细胞白血病的自体BMT预后与异基因BMT相当。