Bordigoni P, Vernant J P, Souillet G, Philippe N, Maraninchi D
Arch Fr Pediatr. 1986 Dec;43(10):765-8.
Sixty-five children with acute lymphoblastic leukemia (ALL) underwent allogenic bone marrow transplantation (BMT) from an HLA identical donor, following cytoreduction with cyclophosphamide and total body irradiation (TBI): 15 were transplanted in 1st remission, 43 in 2nd and 7 in 3rd or in 4th. The Kaplan Meier estimate of surviving disease free at 4 years post BMT was 49.9% and the probability of continued remission at 4 years was 63.3%. Fourteen patients relapsed between 90 and 690 days (mean: 240 +/- 88) post BMT. The other causes of BMP failure included: graft versus host disease, veno-occlusive disease and sepsis. No interstitial pneumonitis has been reported. Patients who had a relapse while on chemotherapy had a higher probability of relapse than those who had a relapse while off therapy (p less than 0.01). We conclude that allogeneic BMT is the treatment of choice for children with ALL in second hematologic remission, the interval between diagnosis and first relapse being the most significant prognostic factor. Patients with poor prognosis might benefit from a more intensive chemotherapy/total body irradiation schedule or a BMT earlier in the course of their disease.
65名急性淋巴细胞白血病(ALL)患儿接受了来自HLA配型相同供者的异基因骨髓移植(BMT),移植前先用环磷酰胺和全身照射(TBI)进行了细胞减灭:15例在第1次缓解期移植,43例在第2次缓解期移植,7例在第3次或第4次缓解期移植。BMT后4年无病生存的Kaplan-Meier估计值为49.9%,4年持续缓解的概率为63.3%。14例患者在BMT后90至690天(平均:240±88天)复发。BMT失败的其他原因包括:移植物抗宿主病、静脉闭塞性疾病和败血症。未报告间质性肺炎。化疗期间复发的患者比未接受治疗时复发的患者复发概率更高(p<0.01)。我们得出结论,异基因BMT是血液学第2次缓解期ALL患儿的首选治疗方法,诊断至首次复发的间隔时间是最重要的预后因素。预后不良的患者可能从更强化的化疗/全身照射方案或疾病进程中更早进行的BMT中获益。