Devine Steven M, Owzar Kouros, Blum William, Mulkey Flora, Stone Richard M, Hsu Jack W, Champlin Richard E, Chen Yi-Bin, Vij Ravi, Slack James, Soiffer Robert J, Larson Richard A, Shea Thomas C, Hars Vera, Sibley Alexander B, Giralt Sergio, Carter Shelly, Horowitz Mary M, Linker Charles, Alyea Edwin P
Steven M. Devine and William Blum, Ohio State University, Columbus, OH; Kouros Owzar, Flora Mulkey, Vera Hars, and Alexander B. Sibley, Alliance Statistics and Data Center, Duke University, Durham; Thomas C. Shea, University of North Carolina, Chapel Hill, NC; Richard M. Stone, Robert J. Soiffer, and Edwin P. Alyea, Dana-Farber Cancer Institute; Yi-Bin Chen, Massachusetts General Hospital, Boston, MA; Jack W. Hsu, University of Florida, Gainesville, FL; Richard E. Champlin, MD Anderson Cancer Research Center, Houston, TX; Ravi Vij, Washington University, St. Louis, MO; James Slack, Mayo Clinic, Scottsdale, AZ; Richard A. Larson, University of Chicago, Chicago, IL; Sergio Giralt, Memorial Sloan Kettering Cancer Center, New York, NY; Shelly Carter, The EMMES Corporation, Bethesda, MD; Mary M. Horowitz, Medical College of Wisconsin, Milwaukee, WI; and Charles Linker, University of California at San Francisco, San Francisco, CA.
J Clin Oncol. 2015 Dec 10;33(35):4167-75. doi: 10.1200/JCO.2015.62.7273. Epub 2015 Nov 2.
Long-term survival rates for older patients with newly diagnosed acute myeloid leukemia (AML) are extremely low. Previous observational studies suggest that allogeneic hematopoietic stem-cell transplantation (HSCT) may improve overall survival (OS) because of lower rates of relapse. We sought to prospectively determine the value of HSCT for older patients with AML in first complete remission.
We conducted a prospective multicenter phase II study to assess the efficacy of reduced-intensity conditioning HSCT for patients between the ages of 60 and 74 years with AML in first complete remission. The primary end point was disease-free survival at 2 years after HSCT. Secondary end points included nonrelapse mortality (NRM), graft-versus-host disease (GVHD), relapse, and OS.
In all, 114 patients with a median age of 65 years received transplantations. The majority (52%) received transplantations from unrelated donors and were given antithymocyte globulin for GVHD prophylaxis. Disease-free survival and OS at 2 years after transplantation were 42% (95% CI, 33% to 52%) and 48% (95% CI, 39% to 58%), respectively, for the entire group and 40% (95% CI, 29% to 55%) and 50% (95% CI, 38% to 64%) for the unrelated donor group. NRM at 2 years was 15% (95% CI, 8% to 21%). Grade 2 to 4 acute GVHD occurred in 9.6% (95% CI, 4% to 15%) of patients, and chronic GVHD occurred in 28% (95% CI, 19% to 36%) of patients. The cumulative incidence of relapse at 2 years was 44% (95% CI, 35% to 53%).
Reduced-intensity conditioning HSCT to maintain remission in selected older patients with AML is relatively well tolerated and appears to provide superior outcomes when compared with historical patients treated without HSCT. GVHD and NRM rates were lower than expected. Future transplantation studies in these patients should focus on further reducing the risk of relapse.
新诊断的急性髓系白血病(AML)老年患者的长期生存率极低。既往观察性研究表明,异基因造血干细胞移植(HSCT)可能因复发率较低而改善总生存期(OS)。我们试图前瞻性地确定HSCT对首次完全缓解的AML老年患者的价值。
我们进行了一项前瞻性多中心II期研究,以评估降低强度预处理HSCT对年龄在60至74岁、首次完全缓解的AML患者的疗效。主要终点是HSCT后2年的无病生存期。次要终点包括非复发死亡率(NRM)、移植物抗宿主病(GVHD)、复发和OS。
共有114例中位年龄为65岁的患者接受了移植。大多数患者(52%)接受了来自无关供者的移植,并接受了抗胸腺细胞球蛋白预防GVHD。整个组移植后2年的无病生存期和OS分别为42%(95%CI,33%至52%)和48%(95%CI,39%至58%),无关供者组分别为40%(95%CI,29%至55%)和50%(95%CI,38%至64%)。2年时的NRM为15%(95%CI,8%至21%)。9.6%(95%CI,4%至15%)的患者发生2至4级急性GVHD,28%(95%CI,19%至36%)的患者发生慢性GVHD。2年时复发的累积发生率为44%(95%CI,35%至53%)。
对于部分选定的AML老年患者,降低强度预处理HSCT维持缓解的耐受性相对较好,与未接受HSCT治疗的历史患者相比,似乎能提供更好的结果。GVHD和NRM发生率低于预期。未来针对这些患者的移植研究应侧重于进一步降低复发风险。