Matthias Stelljes, Utz Krug, Maria C. Sauerland, Achim Heinecke, Sandra Ligges, Tim Sauer, Petra Tschanter, Gabriela B. Thoennissen, Björna Berning, Carsten Müller-Tidow, Wolfgang E. Berdel, and Thomas Büchner, University Hospital of Muenster, Muenster; Dietrich W. Beelen, University Hospital of Essen, Essen; Jan Braess, Krankenhaus Barmherzige Brüder; Albrecht Reichle, Ernst Holler, University of Regensburg, Regensburg; Hans J. Kolb, Wolfgang Hiddeman, University of Munich-Grosshadern, Munich; Rainer Schwerdtfeger, Deutsche Klinik für Diagnostik, Wiesbaden; Renate Arnold, Charité, Universitätsmedizin Berlin, Campus Virchow-Klinikum; Bernhard J. Woermann, German Society of Hematology and Oncology, Berlin; and Christoph Scheid, University of Cologne, Cologne, Germany.
J Clin Oncol. 2014 Feb 1;32(4):288-96. doi: 10.1200/JCO.2013.50.5768. Epub 2013 Dec 23.
The majority of patients with acute myeloid leukemia (AML) who achieve complete remission (CR) relapse with conventional postremission chemotherapy. Allogeneic stem-cell transplantation (alloSCT) might improve survival at the expense of increased toxicity. It remains unknown for which patients alloSCT is preferable.
We compared the outcome of 185 matched pairs of a large multicenter clinical trial (AMLCG99). Patients younger than 60 years who underwent alloSCT in first remission (CR1) were matched to patients who received conventional postremission therapy. The main matching criteria were AML type, cytogenetic risk group, patient age, and time in first CR.
In the overall pairwise compared AML population, the projected 7-year overall survival (OS) rate was 58% for the alloSCT and 46% for the conventional postremission treatment group (P = .037; log-rank test). Relapse-free survival (RFS) was 52% in the alloSCT group compared with 33% in the control group (P < .001). OS was significantly better for alloSCT in patient subgroups with nonfavorable chromosomal aberrations, patients older than 45 years, and patients with secondary AML or high-risk myelodysplastic syndrome. For the entire patient cohort, postremission therapy was an independent factor for OS (hazard ratio, 0.66; 95% CI, 0.49 to 0.89 for alloSCT v conventional chemotherapy), among age, cytogenetics, and bone marrow blasts after the first induction cycle.
AlloSCT is the most potent postremission therapy for AML and is particularly active for patients 45 to 59 years of age and/or those with high-risk cytogenetics.
大多数达到完全缓解(CR)的急性髓系白血病(AML)患者在接受常规缓解后化疗后会复发。异基因造血干细胞移植(alloSCT)可能会提高生存率,但毒性也会增加。对于哪些患者适合 alloSCT 仍不清楚。
我们比较了来自大型多中心临床试验(AMLCG99)的 185 对匹配的患者的结果。年龄在 60 岁以下的患者在首次缓解(CR1)时接受 alloSCT 与接受常规缓解后治疗的患者进行匹配。主要匹配标准是 AML 类型、细胞遗传学风险组、患者年龄和首次 CR 时间。
在整体配对比较的 AML 人群中,alloSCT 组的 7 年总生存率(OS)预计为 58%,常规缓解后治疗组为 46%(P =.037;对数秩检验)。alloSCT 组的无复发生存率(RFS)为 52%,对照组为 33%(P <.001)。alloSCT 在非有利染色体异常、年龄大于 45 岁、继发性 AML 或高危骨髓增生异常综合征的患者亚组中 OS 显著更好。对于整个患者队列,缓解后治疗是 OS 的独立因素(风险比,0.66;95%CI,alloSCT 与常规化疗相比为 0.49 至 0.89),年龄、细胞遗传学和首次诱导周期后骨髓原始细胞计数均有影响。
alloSCT 是 AML 最有效的缓解后治疗方法,对于 45 至 59 岁及/或具有高危细胞遗传学的患者尤其有效。