Petersen F B, Lynch M H, Clift R A, Appelbaum F R, Sanders J E, Bensinger W I, Benyunes M C, Doney K, Fefer A, Martin P
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
J Clin Oncol. 1993 Jul;11(7):1353-60. doi: 10.1200/JCO.1993.11.7.1353.
This study compares outcomes of autologous bone marrow transplantation (ABMT) in patients with acute myeloid leukemia (AML) in untreated first relapse (REL1) or in second complete remission (REM2).
Forty-seven patients with AML in REL1 (n = 21) or in REM2 (n = 26) were treated with busulfan (BU) and cyclophosphamide (CY) with or without total-body irradiation (TBI) followed by ABMT. All REL1 patients and four REM2 patients had marrow stored during first remission (REM1). Twenty-seven had marrow stored with and 20 without treatment in vitro with 4-hydroperoxycyclophosphamide (4-HC). Eighteen patients received BU and CY and 29 received BU, CY, and TBI. REL1 patients relapsed within a median of 9 months (range, 2 to 26) after marrow harvest and were transplanted a median of 30 days (range, 9 to 87) from detection of relapse.
With a median follow-up of 2.1 years (range, 0.4 to 5.3), 19 patients survive in remission (10 of 21 in REL1; nine of 26 in REM2). The actuarial probabilities of relapse-free survival at 2 years for patients transplanted in REL1 and REM2 were 45% +/- 22% and 32% +/- 18%, respectively (P = .33). The corresponding probabilities of relapse were 30% +/- 26% and 44% +/- 23%, respectively (P = .45). No conclusions could be drawn about the benefits of adding TBI to BU plus CY. There were no significant differences in neutrophil or platelet recovery or in posttransplant probabilities of relapse and nonrelapse mortality between patients who received marrow treated or not treated with 4-HC.
These results suggest that ABMT may produce long-term leukemia-free survival in approximately one third of patients with AML in REL1 or in REM2. There is no apparent clinical advantage in attempting to obtain second remissions in relapsed patients before ABMT if marrow has been cryopreserved during REM1. Although a strategy of transplantation in REL1 has advantages for the patient, such an approach involves the storage of marrow, which may not be used, and is impractical without the coordinated support of the treating physician, the patient, and the marrow transplant center.
本研究比较急性髓系白血病(AML)患者在首次未缓解复发(REL1)或第二次完全缓解(REM2)时进行自体骨髓移植(ABMT)的结果。
47例AML患者,其中REL1组21例,REM2组26例,接受白消安(BU)和环磷酰胺(CY)治疗,部分联合全身照射(TBI),随后进行ABMT。所有REL1患者及4例REM2患者在首次缓解期(REM1)储存了骨髓。27例患者的骨髓在体外经4 - 氢过氧环磷酰胺(4 - HC)处理,20例未处理。18例患者接受BU和CY治疗,29例接受BU、CY及TBI治疗。REL1患者在骨髓采集后中位9个月(范围2至26个月)复发,从复发检测到移植的中位时间为30天(范围9至87天)。
中位随访2.1年(范围0.4至5.3年),19例患者缓解生存(REL1组21例中的10例;REM2组26例中的9例)。REL1组和REM2组移植患者2年无复发生存的精算概率分别为45%±22%和32%±18%(P = 0.33)。相应的复发概率分别为30%±26%和44%±23%(P = 0.45)。关于在BU加CY基础上加用TBI的益处无法得出结论。接受4 - HC处理或未处理骨髓的患者,在中性粒细胞或血小板恢复、移植后复发及非复发死亡率方面无显著差异。
这些结果表明,ABMT可能使约三分之一的AML患者在REL1或REM2时获得长期无白血病生存。如果在REM1期间已冷冻保存骨髓,对于复发患者在ABMT前试图获得第二次缓解并无明显临床优势。虽然在REL1期进行移植的策略对患者有优势,但这种方法需要储存骨髓,而骨髓可能无法使用,且若无治疗医生、患者及骨髓移植中心的协调支持则不切实际。