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自体造血干细胞移植治疗复发性肾母细胞瘤患者的结果:CIBMTR 回顾性分析。

Outcomes following autologous hematopoietic stem cell transplant for patients with relapsed Wilms' tumor: a CIBMTR retrospective analysis.

机构信息

Davis Cancer Center, University of California, Sacramento, CA, USA.

CIBMTR (Center for International Blood and Marrow Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Bone Marrow Transplant. 2017 Nov;52(11):1549-1555. doi: 10.1038/bmt.2017.178. Epub 2017 Sep 4.

Abstract

Despite the marked improvement in the overall survival (OS) for patients diagnosed with Wilms' tumor (WT), the outcomes for those who experience relapse have remained disappointing. We describe the outcomes of 253 patients with relapsed WT who received high-dose chemotherapy (HDT) followed by autologous hematopoietic stem cell transplant (HCT) between 1990 and 2013, and were reported to the Center for International Blood and Marrow Transplantation Research. The 5-year estimates for event-free survival (EFS) and OS were 36% (95% confidence interval (CI); 29-43%) and 45% (95 CI; 38-51%), respectively. Relapse of primary disease was the cause of death in 81% of the population. EFS, OS, relapse and transplant-related mortality showed no significant differences when broken down by disease status at transplant, time from diagnosis to transplant, year of transplant or conditioning regimen. Our data suggest that HDT followed by autologous HCT for relapsed WT is well tolerated and outcomes are similar to those reported in the literature. As attempts to conduct a randomized trial comparing maintenance chemotherapy with consolidation versus HDT followed by stem cell transplant have failed, one should balance the potential benefits with the yet unknown long-term risks. As disease recurrence continues to be the most common cause of death, future research should focus on the development of consolidation therapies for those patients achieving complete response to therapy.

摘要

尽管 Wilms 瘤 (WT) 患者的总体生存率 (OS) 有显著改善,但复发患者的预后仍然令人失望。我们描述了 1990 年至 2013 年间 253 例接受大剂量化疗 (HDT) 后进行自体造血干细胞移植 (HCT) 的复发 WT 患者的结果,并向国际血液和骨髓移植研究中心报告。无事件生存 (EFS) 和 OS 的 5 年估计值分别为 36%(95%置信区间[CI]:29-43%)和 45%(95%CI:38-51%)。81%的患者因原发性疾病复发而死亡。按移植时疾病状态、诊断至移植时间、移植年份或预处理方案进行分层后,EFS、OS、复发和移植相关死亡率没有显著差异。我们的数据表明,复发 WT 患者接受 HDT 后行自体 HCT 治疗耐受性良好,且结果与文献报道相似。由于尝试进行维持化疗与巩固治疗与 HDT 后行干细胞移植的随机试验均以失败告终,因此应权衡潜在益处与未知的长期风险。由于疾病复发仍然是最常见的死亡原因,未来的研究应集中于为那些对治疗完全有反应的患者开发巩固治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f72d/5665725/8e89db7cf0c4/nihms885619f1.jpg

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