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多发性骨髓瘤自体和异基因造血细胞移植治疗的结果

Results of autologous and allogeneic hematopoietic cell transplant therapy for multiple myeloma.

作者信息

Arora M, McGlave P B, Burns L J, Miller J S, Barke J N, Defor T E, Weisdorf D J

机构信息

Division of Hematology, Oncology and Transplantation, Department of Medicine, and the Blood and Marrow Transplant Program, University of Minnesota, MN 55455, USA.

出版信息

Bone Marrow Transplant. 2005 Jun;35(12):1133-40. doi: 10.1038/sj.bmt.1704968.

Abstract

We compared the results of autologous and allogeneic peripheral blood hematopoietic cell transplant (HCT) in 87 patients with multiple myeloma using myeloablative preparative regimen. Autologous transplant (n=70) led to a lower 100-day transplant-related mortality (TRM) of 4% [0-9%] compared to 18% [0-36%] in allogeneic recipients (P=0.02). More frequent complete responses were seen in allogeneic recipients (64% [37-91%] vs 34% [23-45%] in autologous recipients, P=0.09). In autologous recipients, survival at 1 year was 86% [80-95%] and, it fell to 50% [47-75%] at 4 years, whereas in allogeneic recipients, survival at 1 and 4 years remained at 64% [40-87%]. In patients surviving more than one year, 4-year survival was superior in allogeneic (100%) vs autologous recipients (58% [41-75%], P=0.02). A trend toward higher relapse was seen in autologous transplant patients (73% [55-90%] vs 37% [11-63%] in allogeneic transplant patients, P=0.1). We observed good tolerance of myeloablative conditioning regimen followed by either autologous or allogeneic transplant. Although autologous HCT is associated with lower TRM, allogeneic HCT has acceptable TRM, and is more likely to provide a sustained response. Allogeneic HCT may be suitable in younger patients, soon after diagnosis, and in those with chemosensitive disease.

摘要

我们使用清髓性预处理方案比较了87例多发性骨髓瘤患者自体和异基因外周血造血细胞移植(HCT)的结果。自体移植(n = 70)导致100天移植相关死亡率(TRM)较低,为4%[0 - 9%],而异基因受体的这一比例为18%[0 - 36%](P = 0.02)。异基因受体中完全缓解更为常见(64%[37 - 91%],自体受体为34%[23 - 45%],P = 0.09)。自体受体1年生存率为86%[80 - 95%],4年时降至50%[47 - 75%],而异基因受体1年和4年生存率分别保持在64%[40 - 87%]。在存活超过1年的患者中,异基因受体的4年生存率更高(100%),高于自体受体(58%[41 - 75%],P = 0.02)。自体移植患者有更高复发率的趋势(73%[55 - 90%],异基因移植患者为37%[11 - 63%],P = 0.1)。我们观察到清髓性预处理方案后进行自体或异基因移植均有良好的耐受性。虽然自体HCT与较低的TRM相关,但异基因HCT的TRM可接受,且更有可能提供持续缓解。异基因HCT可能适用于诊断后不久的年轻患者以及对化疗敏感的疾病患者。

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