Rowe Jacob M, Buck Georgina, Burnett Alan K, Chopra Raj, Wiernik Peter H, Richards Susan M, Lazarus Hillard M, Franklin Ian M, Litzow Mark R, Ciobanu Niculae, Prentice H Grant, Durrant Jill, Tallman Martin S, Goldstone Anthony H
Department of Hematology and Bone Marrow Transplantation, Rambam Medical Center and Technion, Israel Institute of Technology, Haifa 31096, Israel.
Blood. 2005 Dec 1;106(12):3760-7. doi: 10.1182/blood-2005-04-1623. Epub 2005 Aug 16.
The international acute lymphoblastic leukemia (ALL) study was designed to prospectively define the optimal therapy for adults 60 years of age or younger with newly diagnosed ALL. All patients received identical induction therapy, and 91% achieved complete remission (CR). Patients 50 years of age or younger with a compatible sibling were assigned to undergo allogeneic transplantation; the others were randomly assigned to autologous transplantation or to consolidation/maintenance therapy for 2.5 years. Patients who did not achieve CR after induction had an overall survival rate of 5% compared with 45% for patients who achieved CR. Factors at diagnosis predictive of overall survival and disease-free survival were age (P = .001), white blood cell count less than 30 x 10(9)/L for B lineage or less than 100 x 10(9)/L for T lineage (P = .001) and immunophenotype, T lineage versus B lineage (P = .001). The data demonstrate that achieving CR with induction therapy is indispensable for long-term survival in adult patients with ALL. Furthermore, with a response rate greater than 90%, the induction regimen was highly efficacious as remission-inducing therapy. This large database has validated several previously identified independent prognostic factors in ALL, such as age, white blood cell count at presentation, cytogenetics, and immunophenotype. However, the achievement of CR within 4 weeks does not appear to be an independent prognostic factor.
国际急性淋巴细胞白血病(ALL)研究旨在前瞻性地确定60岁及以下新诊断ALL成年患者的最佳治疗方案。所有患者均接受相同的诱导治疗,91%的患者实现完全缓解(CR)。50岁及以下有匹配同胞供者的患者被分配接受异基因移植;其他患者则被随机分配接受自体移植或进行2.5年的巩固/维持治疗。诱导治疗后未达到CR的患者总生存率为5%,而达到CR的患者为45%。诊断时预测总生存和无病生存的因素包括年龄(P = .001)、B系白细胞计数低于30×10⁹/L或T系低于100×10⁹/L(P = .001)以及免疫表型,T系与B系(P = .001)。数据表明,诱导治疗实现CR对于ALL成年患者的长期生存不可或缺。此外,诱导方案作为缓解诱导治疗,缓解率大于90%,疗效显著。这个大型数据库验证了ALL中几个先前确定的独立预后因素,如年龄、就诊时白细胞计数、细胞遗传学和免疫表型。然而,4周内达到CR似乎不是一个独立的预后因素。