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对于反应性骨髓瘤患者,使用美法仑加全身照射(MEL-TBI)或环磷酰胺(MEL-CY)作为预处理方案并进行第二次自体移植,与仅接受美法仑串联移植的历史对照相比效果较差。

Melphalan plus total body irradiation (MEL-TBI) or cyclophosphamide (MEL-CY) as a conditioning regimen with second autotransplant in responding patients with myeloma is inferior compared to historical controls receiving tandem transplants with melphalan alone.

作者信息

Desikan K R, Tricot G, Dhodapkar M, Fassas A, Siegel D, Vesole D H, Jagannath S, Singhal S, Mehta J, Spoon D, Anaissie E, Barlogie B, Munshi N

机构信息

Myeloma and Transplantation Research Center, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

出版信息

Bone Marrow Transplant. 2000 Mar;25(5):483-7. doi: 10.1038/sj.bmt.1702167.

Abstract

The role of more intense conditioning for second transplant was evaluated in myeloma patients achieving at least partial remission (PR) after first transplant with melphalan at 200 mg/m2. Forty-three patients received more intensive conditioning for the second transplant. Nineteen patients received cyclophosphamide 120 mg/kg along with melphalan 200 g/m2 (MEL-CY; group 1) while 24 patients received total body irradiation (1125 cGy) in conjunction with melphalan 140 mg/m2 (MEL-TBI; group 2). Forty-three matched control patients were identified from 450 patients receiving melphalan alone for second transplant (MEL200; group 3). Engraftment and toxicities were comparable among the groups with the exception of increased treatment-related mortality of 8% in group 2 compared to none in groups 1 and 3 (P = 0.07). Despite identical CR rates of 74, 71 and 70%, respectively, in groups 1, 2 and 3 (P = 1.0), event-free survival (median: 27, 15 and 61; P < 0.0001) and overall survival (median: 39, 25 and 76 months; P = 0.003) were significantly decreased in patients receiving more intensive conditioning (groups 1 and 2). Lymphocyte recovery, evaluated as a surrogate for immune recovery, was inferior in more intensively treated patients (groups 1 and 2 compared to group 3). Our findings suggest that more intense conditioning appears to have no benefit in patients responding to their first cycle of high-dose therapy and may even be detrimental in this setting. Bone Marrow Transplantation (2000) 25, 483-487.

摘要

在接受200mg/m²马法兰首次移植后至少达到部分缓解(PR)的骨髓瘤患者中,评估了更强烈预处理方案对二次移植的作用。43例患者接受了更强烈的二次移植预处理。19例患者接受120mg/kg环磷酰胺联合200mg/m²马法兰(MEL-CY;第1组),而24例患者接受全身照射(1125cGy)联合140mg/m²马法兰(MEL-TBI;第2组)。从450例接受单纯马法兰二次移植的患者中确定了43例匹配对照患者(MEL200;第3组)。除第2组与第1组和第3组中无治疗相关死亡相比有8%的治疗相关死亡率增加外(P = 0.07),各组间的植入和毒性相当。尽管第1、2和3组的完全缓解率分别相同,均为74%、71%和70%(P = 1.0),但接受更强烈预处理的患者(第1组和第2组)的无事件生存期(中位数:27、15和61;P < 0.0001)和总生存期(中位数:39、25和76个月;P = 0.003)显著降低。作为免疫恢复替代指标评估的淋巴细胞恢复情况,在接受更强烈治疗的患者中较差(第1组和第2组与第3组相比)。我们的研究结果表明,更强烈的预处理对首次高剂量治疗有反应的患者似乎没有益处,甚至在这种情况下可能有害。《骨髓移植》(2000年)25卷,483 - 487页 。

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