Yoo Shin Hye, Koh Youngil, Kim Dae-Young, Lee Jung-Hee, Lee Je-Hwan, Lee Kyoo-Hyung, Yoon Sung-Soo, Park Seonyang, Park Sung-Kyu, Hong Dae-Sik, Yi Hyeon Gyu, Kim Chul-Soo, Jang Ji Eun, Cheong June-Won, Moon Joonho, Min Yoo Hong, Sohn Sang Kyun, Kim Inho
Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, 101 Daehak-ro, Chongno-gu, Seoul, 110-744, South Korea.
Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Ann Hematol. 2017 Apr;96(4):605-615. doi: 10.1007/s00277-017-2919-8. Epub 2017 Jan 16.
Little is known about the characteristics that make patients with acute leukemia suitable for undergoing salvage therapy by allogeneic hematopoietic stem cell transplantation (allo-HSCT). Here, we analyzed the clinical outcomes of 223 patients with acute leukemia who underwent allo-HSCT while not in complete remission (CR). The primary end points were overall survival (OS) and CR rate. CR was achieved in 79.8% of patients after allo-HSCT. Acute graft-versus-host disease (GVHD) was significantly associated with CR (P = 0.045). During a median follow-up of 30.1 months, the median OS was 6.1 months. OS was significantly longer in patients with good or standard risk cytogenetic characteristics than in those with poor risk cytogenetic characteristics (P = 0.029, P = 0.030, respectively). Patients who received allo-HSCT from a matched sibling donor had better survival than those with unrelated donors (P = 0.015). Primary chemorefractoriness was not associated with poor survival (P = 0.071). The number of chemotherapies before allo-HSCT was significantly correlated with outcome (P = 0.006). Chronic GVHD was a strong predictor of a longer OS (P = 0.025). In conclusion, survival of patients with primary chemorefractory acute leukemia is not lower when treated upfront with allo-HSCT. Hence, allo-HSCT should be actively considered in such patients. Acute and chronic GVHD is associated with better outcomes patients with acute leukemia who have undergone allo-HSCT and not achieved CR.
关于使急性白血病患者适合接受异基因造血干细胞移植(allo-HSCT)挽救治疗的特征,目前所知甚少。在此,我们分析了223例未完全缓解(CR)时接受allo-HSCT的急性白血病患者的临床结局。主要终点是总生存期(OS)和CR率。allo-HSCT后79.8%的患者实现了CR。急性移植物抗宿主病(GVHD)与CR显著相关(P = 0.045)。在中位随访30.1个月期间,中位OS为6.1个月。细胞遗传学特征为良好或标准风险的患者的OS明显长于细胞遗传学特征为不良风险的患者(分别为P = 0.029,P = 0.030)。接受来自匹配同胞供体的allo-HSCT的患者比接受无关供体的患者生存情况更好(P = 0.015)。原发性化疗耐药与生存不良无关(P = 0.071)。allo-HSCT前化疗的次数与结局显著相关(P = 0.006)。慢性GVHD是OS更长的有力预测因素(P = 0.025)。总之,原发性化疗难治性急性白血病患者在接受allo-HSCT一线治疗时生存率并不低。因此,对此类患者应积极考虑allo-HSCT。急性和慢性GVHD与接受allo-HSCT且未达到CR的急性白血病患者的较好结局相关。