Abe T, Takaue Y, Matsunaga K, Saito S, Hirao A, Okamoto Y, Nakanishi J, Watanabe T, Kawano Y, Ninomiya T
Department of Pediatrics, University Hospital of Tokushima.
Rinsho Ketsueki. 1991 Nov;32(11):1425-32.
Thirty children (1-16 y.o.; median, 10 y.o.) with acute leukemia or non-Hodgkin's lymphoma (NHL) associated with high-risk features underwent high-dose chemotherapy without total body irradiation and peripheral blood stem cell autografts (PBSCT). Eighteen patients had acute lymphoblastic leukemia (ALL), 6 had acute non-lymphoblastic leukemia (ANLL), 2 had mixed-lineage leukemia and 4 had NHL. Twelve patients with two or more high-risk features (WBC greater than 10 x 10(4)/microliter, T- or B-phenotypes, infancy, massive organ infiltration, or induction failure) underwent PBSCT in 1st CR. Twelve patients underwent PBSCT in 2nd CR, and 4 in the subsequent remission greater than or equal to 3rd CR). Two patients were treated at refractory relapse. After PBSCT the number of days required to achieve a granulocyte count of 0.5 x 10(9)/l and a platelet count of 50 x 10(9)/l was 6.39 (median, 13) and 9-427 (median, 16), respectively. The disease-free survival rate was 6/12 in 1st CR group (6-41 mo) and 6/16 in the patients who underwent PBSCT in 2nd or subsequent remission (2-35 mo). The data justify the incorporation of PBSCT in the design of salvage protocol for children with leukemias or NHL. However, the application of the procedure as part of initial therapy in patients still remaining in 1st CR should be regarded as highly experimental and deserve further clarification.
30名患有急性白血病或伴有高危特征的非霍奇金淋巴瘤(NHL)的儿童(年龄1 - 16岁;中位数为10岁)接受了不含全身照射的大剂量化疗及外周血干细胞自体移植(PBSCT)。18例为急性淋巴细胞白血病(ALL),6例为急性非淋巴细胞白血病(ANLL),2例为混合谱系白血病,4例为NHL。12例具有两项或更多高危特征(白细胞大于10×10⁴/微升、T或B表型、婴儿期、大量器官浸润或诱导失败)的患者在首次完全缓解(CR)时接受了PBSCT。12例患者在第二次CR时接受了PBSCT,4例在后续大于或等于第三次CR的缓解期接受了PBSCT。2例患者在难治性复发时接受了治疗。PBSCT后,粒细胞计数达到0.5×10⁹/L和血小板计数达到50×10⁹/L所需的天数分别为6.39(中位数为13)和9 - 427(中位数为16)。首次CR组的无病生存率为6/12(6 - 41个月),在第二次或后续缓解期接受PBSCT的患者中为6/16(2 - 35个月)。这些数据证明在白血病或NHL儿童的挽救方案设计中纳入PBSCT是合理的。然而,将该程序作为仍处于首次CR的患者初始治疗的一部分应用应被视为高度实验性的,值得进一步阐明。