Kohno Akio, Morishita Yoshihisa, Iida Hiroatsu, Yanada Masamitsu, Uchida Toshiki, Hamaguchi Motohiro, Sawa Masashi, Sugiura Isamu, Yamamoto Kazuhito, Mizuta Shuichi, Sao Hiroshi, Naoe Tomoki, Miyamura Koichi
Division of Hematology and Oncology, JA Aichi Showa Hospital, 46 Nobaku, Nobaku-cho, Konan, Aichi, 483-8703, Japan.
Department of Hematology, Meitetsu Hospital, Nagoya, Japan.
Int J Hematol. 2008 Mar;87(2):210-216. doi: 10.1007/s12185-008-0020-8. Epub 2008 Feb 28.
Acute promyelocytic leukemia (APL) is the most curable subtype of acute myeloid leukemia. Second complete remission (CR2) can be easily achieved with several therapeutic options even after relapse. However, the optimal strategy to treat APL in CR2 is still controversial. We retrospectively compared the outcome of autologous (auto) and allogeneic (allo) hematopoietic stem cell transplantation (HSCT) for patients with APL in CR2 or CR3. Fifteen patients received auto and 13 received allo HSCT between 1999 and 2004 at eight hospitals belonging to the Nagoya Blood and Marrow Transplantation Group. Four-year disease-free survival (DFS) and overall survival (OS) for autografted patients were 68.9 and 75.8%, whereas those for allografted patients were 46.2 (P = 0.350) and 46.2% (P = 0.185), respectively. Three autografted patients and one allografted patient relapsed, and one autografted patient and five allografted patients died without leukemia relapse. Among 14 autografted patients who were evaluated for MRD with molecular analysis, relapse occurred in one with positive MRD (n = 2) and two with negative MRD (n = 12). These data suggest that auto HSCT is very effective for APL in CR2 or CR3, and may be preferable to allo HSCT for a portion of patients. Prospective studies are required to define the role of auto HSCT in the treatment of relapsed APL.
急性早幼粒细胞白血病(APL)是急性髓系白血病中最可治愈的亚型。即使复发后,通过多种治疗方案也能轻松实现第二次完全缓解(CR2)。然而,治疗处于CR2期的APL的最佳策略仍存在争议。我们回顾性比较了自体(auto)和异基因(allo)造血干细胞移植(HSCT)对处于CR2或CR3期的APL患者的疗效。1999年至2004年期间,在名古屋血液和骨髓移植组所属的八家医院中,15例患者接受了自体HSCT,13例患者接受了异基因HSCT。自体移植患者的4年无病生存率(DFS)和总生存率(OS)分别为68.9%和75.8%,而异基因移植患者的4年DFS和OS分别为46.2%(P = 0.350)和46.2%(P = 0.185)。3例自体移植患者和1例异基因移植患者复发,1例自体移植患者和5例异基因移植患者在无白血病复发的情况下死亡。在14例接受分子分析评估微小残留病(MRD)的自体移植患者中,1例MRD阳性(n = 2)和2例MRD阴性(n = 12)的患者复发。这些数据表明,自体HSCT对处于CR2或CR3期的APL非常有效,对于一部分患者可能比异基因HSCT更可取。需要进行前瞻性研究来确定自体HSCT在复发APL治疗中的作用。