Blau I W, Basara N, Bischoff M, Günzelmann S, Römer E, Kirsten D, Schmetzer B, Kiehl M G, Fauser A A
Clinic for Bone Marrow Transplantation and Hematology/Oncology, Idar-Oberstein, Germany.
Bone Marrow Transplant. 2000 Jan;25(1):41-5. doi: 10.1038/sj.bmt.1702101.
We report 27 patients with relapsed acute or chronic leukemia who underwent a second hematopoietic stem cell transplant (HSCT) from a related or unrelated donor. Seventeen patients were diagnosed with acute myelogenous leukemia (AML), six with acute lymphocytic leukemia (ALL) and four with chronic myeloid leukemia (CML). Ages ranged from 22 to 49 years (median 37); 13 patients were female and 14 male. Relapse was diagnosed between 1 and 45 months after the first HSCT. Sixteen patients who relapsed had received an autologous transplant initially and 11 an allogeneic transplant. Ten patients relapsed within 6 months and 17 patients later than 6 months. Chemotherapy was used as reinduction for relapse after HSCT in 16 patients who had received an autologous transplant and in three who had received an allogeneic transplant, since the latter did not respond to reduction of immunosuppression to induce a graft-versus-leukemia (GVL) reaction. Five of these 19 patients (26%) achieved complete remission (CR), seven patients did not respond to chemotherapy and seven achieved a partial remission (PR). The stem cell source for the second HSCT included bone marrow (n = 12) and PBSC (n = 4) from genotypically identical unrelated donors, PBSC (n = 7) and bone marrow (n = 3) from related donors. Currently eight of the 27 patients are alive and disease-free after the second HSCT. One patient is alive and disease-free after two allogeneic transplants (day +1538), eight patients, who relapsed after an autologous transplant followed by an allogeneic transplant (days +248 to +1140), acute myeloid leukaemia (n = 6) and chronic myeloid leukemia (n = 2) are alive and disease-free. The overall disease-free survival is 30% (8/27). The overall disease-free survival of autologous transplant patients subsequently undergoing an allogeneic transplant is 43% (P = 0.049). It is suggested that a second HSCT is possible for patients with leukemia relapse following the first autologous transplant. A second transplant might also be offered to patients relapsing after the first allogeneic HSCT. Bone Marrow Transplantation (2000) 25, 41-45.
我们报告了27例复发的急性或慢性白血病患者,他们接受了来自相关或无关供者的第二次造血干细胞移植(HSCT)。17例患者被诊断为急性髓性白血病(AML),6例为急性淋巴细胞白血病(ALL),4例为慢性髓性白血病(CML)。年龄范围为22至49岁(中位数37岁);13例为女性,14例为男性。复发在首次HSCT后1至45个月被诊断。16例复发患者最初接受了自体移植,11例接受了异基因移植。10例患者在6个月内复发,17例在6个月后复发。16例接受自体移植和3例接受异基因移植的患者在HSCT后复发时接受了化疗作为再诱导治疗,因为后者对降低免疫抑制以诱导移植物抗白血病(GVL)反应无反应。这19例患者中有5例(26%)达到完全缓解(CR),7例对化疗无反应,7例达到部分缓解(PR)。第二次HSCT的干细胞来源包括来自基因相同的无关供者的骨髓(n = 12)和外周血干细胞(PBSC,n = 4)、来自相关供者的PBSC(n = 7)和骨髓(n = 3)。目前,27例患者中有8例在第二次HSCT后存活且无疾病。1例患者在两次异基因移植后存活且无疾病(+1538天),8例在自体移植后复发随后接受异基因移植的患者(+248至+1140天),急性髓性白血病(n = 6)和慢性髓性白血病(n = 2)存活且无疾病。总体无病生存率为30%(8/27)。随后接受异基因移植的自体移植患者的总体无病生存率为43%(P = 0.049)。提示对于首次自体移植后复发的白血病患者,第二次HSCT是可行的。对于首次异基因HSCT后复发的患者也可考虑进行第二次移植。《骨髓移植》(2000年)25卷,41 - 45页 。