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多发性骨髓瘤的异基因骨髓移植。欧洲骨髓移植组

Allogeneic bone marrow transplantation in multiple myeloma. European Group for Bone Marrow Transplantation.

作者信息

Gahrton G, Tura S, Ljungman P, Belanger C, Brandt L, Cavo M, Facon T, Granena A, Gore M, Gratwohl A

机构信息

Department of Medicine, Huddinge Hospital, Sweden.

出版信息

N Engl J Med. 1991 Oct 31;325(18):1267-73. doi: 10.1056/NEJM199110313251802.

Abstract

BACKGROUND AND METHODS

In contrast to autologous bone marrow transplants for hematologic cancers, allogeneic transplants contain no tumor cells that might cause a relapse. We report the results of such allogeneic bone marrow transplantation using HLA-compatible sibling donors in 90 patients with multiple myeloma performed in 26 European centers between 1983 and 1989.

RESULTS

At the time of the most recent follow-up, 79 months after the start of the study, 47 patients were alive and 43 were dead. The rate of complete remission after bone marrow transplantation was 43 percent for all patients and 58 percent for the patients who had engraftment. The actuarial survival at 76 months was 40 percent. The median duration of relapse-free survival among patients who were in complete remission after bone marrow transplantation was 48 months. The stage of the disease at diagnosis and the number of treatment regimens tried before bone marrow transplantation were predictive of the likelihood of complete remission after engraftment. There were trends toward longer survival among patients who were responsive to treatment before bone marrow transplantation, patients with Stage I disease at diagnosis, and patients who had received only first-line treatment before transplantation, as compared with those who were not responsive, those with Stage II or III disease at diagnosis, and those who had received three or more lines of treatment, but the differences in these factors were not statistically significant. Two post-transplantation factors predicted better long-term survival: complete remission after engraftment and grade I graft-versus-host disease, rather than grade II, III, or IV.

CONCLUSIONS

Allogeneic bone marrow transplantation with the use of HLA-matched sibling donors appears to be a promising method of treatment for some patients with multiple myeloma.

摘要

背景与方法

与用于血液系统癌症的自体骨髓移植不同,异基因移植不含可能导致复发的肿瘤细胞。我们报告了1983年至1989年间在26个欧洲中心对90例多发性骨髓瘤患者使用HLA匹配的同胞供体进行异基因骨髓移植的结果。

结果

在研究开始79个月后的最近一次随访时,47例患者存活,43例死亡。所有患者骨髓移植后的完全缓解率为43%,植入成功的患者为58%。76个月时的精算生存率为40%。骨髓移植后处于完全缓解的患者中,无复发生存期的中位数为48个月。诊断时疾病的分期以及骨髓移植前尝试的治疗方案数量可预测植入后完全缓解的可能性。与未缓解者、诊断时为II期或III期疾病者以及移植前接受过三线或更多线治疗者相比,骨髓移植前对治疗有反应的患者、诊断时为I期疾病的患者以及移植前仅接受一线治疗的患者有生存时间更长的趋势,但这些因素的差异无统计学意义。两个移植后因素预示着更好的长期生存:植入后完全缓解和I级移植物抗宿主病,而非II级、III级或IV级。

结论

使用HLA匹配的同胞供体进行异基因骨髓移植似乎是治疗某些多发性骨髓瘤患者的一种有前景的方法。

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