Kersey J H, Weisdorf D, Nesbit M E, LeBien T W, Woods W G, McGlave P B, Kim T, Vallera D A, Goldman A I, Bostrom B
N Engl J Med. 1987 Aug 20;317(8):461-7. doi: 10.1056/NEJM198708203170801.
Chemoradiotherapy and transplantation of bone marrow from matched sibling donors have been useful for the treatment of acute lymphoblastic leukemia in patients with a poor prognosis but are not available to some two thirds of patients who do not have a matched allogeneic donor. We undertook this study to compare autologous and allogeneic marrow transplantation in the treatment of such cases. We treated 91 patients with high-dose chemoradiotherapy and followed them for 1.4 to 5 years. Forty-six patients with an HLA-matched donor received allogeneic marrow, and 45 patients without a matched donor received their own marrow taken during remission and purged of leukemic cells with use of monoclonal antibodies. Bone marrow engraftment occurred earlier in patients who received autologous marrow. Recipients of autologous marrow had shorter hospital courses, with significantly fewer peritransplantation deaths than recipients of allogeneic marrow. Post-transplantation relapse of leukemia was the most frequent cause of treatment failure; relapses occurred in an estimated 37 percent of patients with allogeneic grafts in whom graft-versus-host disease developed, 75 percent of patients with allogeneic grafts in whom graft-versus-host disease did not develop, and 79 percent of patients who received autologous grafts. The interval before relapse was significantly shorter in the autologous-marrow group than in the allogeneic-marrow group. Recipients of autologous and allogeneic marrow whose first pretransplantation remissions were short (less than 18 months) had eventual outcomes similar to those whose first remissions were longer than 18 months. Patients with a first remission lasting less than 18 months had an outcome better than that expected with chemotherapy alone. The fractions of "cured" patients were estimated to be 20 percent in the autologous-marrow group and 27 percent in the allogeneic-marrow group--not a significant difference, but because of the limited statistical power of the study, the question of long-term disease-free survival must still be considered open.
化疗放疗以及来自匹配同胞供者的骨髓移植,对于预后较差的急性淋巴细胞白血病患者的治疗是有效的,但约三分之二没有匹配的异基因供者的患者无法采用这种治疗方法。我们开展这项研究以比较自体和异基因骨髓移植在这类病例治疗中的效果。我们对91例患者进行了大剂量化疗放疗,并对他们随访了1.4至5年。46例有HLA匹配供者的患者接受了异基因骨髓移植,45例没有匹配供者的患者接受了在缓解期采集并经单克隆抗体清除白血病细胞的自身骨髓移植。接受自体骨髓移植的患者骨髓植入更早。自体骨髓移植受者的住院时间更短,移植期间死亡人数明显少于异基因骨髓移植受者。白血病移植后复发是治疗失败最常见的原因;据估计,发生移植物抗宿主病的异基因移植患者中约37%复发,未发生移植物抗宿主病的异基因移植患者中75%复发,接受自体移植的患者中79%复发。自体骨髓移植组复发前的间隔时间明显短于异基因骨髓移植组。首次移植前缓解期短(少于18个月)的自体和异基因骨髓移植受者的最终结局与首次缓解期长于18个月的受者相似。首次缓解期持续少于18个月的患者结局优于单纯化疗预期的结局。自体骨髓移植组和异基因骨髓移植组“治愈”患者的比例估计分别为20%和27%——差异不显著,但由于该研究的统计学效力有限,长期无病生存的问题仍有待探讨。