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来那度胺维持治疗异基因造血细胞移植后的高危多发性骨髓瘤。

Lenalidomide maintenance for high-risk multiple myeloma after allogeneic hematopoietic cell transplantation.

作者信息

Alsina Melissa, Becker Pamela S, Zhong Xiaobo, Adams Alexia, Hari Parameswaran, Rowley Scott, Stadtmauer Edward A, Vesole David H, Logan Brent, Weisdorf Daniel, Qazilbash Muzaffar, Popplewell Leslie L, McClune Brian, Bensinger William, Riches Marcie, Giralt Sergio A, Pasquini Marcelo C

机构信息

Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.

Division of Hematology, University of Washington School of Medicine/Fred Hutchinson Cancer Research Center, Seattle, Washington.

出版信息

Biol Blood Marrow Transplant. 2014 Aug;20(8):1183-9. doi: 10.1016/j.bbmt.2014.04.014. Epub 2014 Apr 21.

Abstract

Allogeneic hematopoietic cell transplantation (alloHCT) with reduced-intensity conditioning is an appealing option for patients with high-risk multiple myeloma (MM). However, progression after alloHCT remains a challenge. Maintenance therapy after alloHCT may offer additional disease control and allow time for a graft-versus-myeloma effect. The primary objective of this clinical trial was to determine the tolerability and safety profile of maintenance lenalidomide (LEN) given on days 1 to 21 of 28 days cycles, with intrapatient dose escalation during 12 months/cycles after alloHCT. Thirty alloHCT recipients (median age, 54 years) with high-risk MM were enrolled at 8 centers between 2009 and 2012. The median time from alloHCT to LEN initiation was 96 days (range, 66 to 171 days). Eleven patients (37%) completed maintenance and 10 mg daily was the most commonly delivered dose (44%). Most common reasons for discontinuation were acute graft-versus-host disease (GVHD) (37%) and disease progression (37%). Cumulative incidence of grades III to IV acute GVHD from time of initiation of LEN was 17%. Outcomes at 18 months after initiation of maintenance were MM progression, 28%; transplantation-related mortality, 11%; and progression-free and overall survival, 63% and 78%, respectively. The use of LEN after alloHCT is feasible at lower doses, although it is associated with a 38% incidence of acute GVHD. Survival outcomes observed in this high-risk MM population warrant further study of this approach.

摘要

采用减低剂量预处理的异基因造血细胞移植(alloHCT)是高危多发性骨髓瘤(MM)患者的一个有吸引力的选择。然而,alloHCT后的疾病进展仍然是一个挑战。alloHCT后的维持治疗可能提供额外的疾病控制,并为移植物抗骨髓瘤效应争取时间。本临床试验的主要目的是确定在28天周期的第1至21天给予来那度胺(LEN)进行维持治疗的耐受性和安全性,在alloHCT后的12个月/周期内进行患者内剂量递增。2009年至2012年期间,8个中心招募了30例高危MM的alloHCT受者(中位年龄54岁)。从alloHCT到开始使用LEN的中位时间为96天(范围66至171天)。11例患者(37%)完成了维持治疗,最常用的给药剂量是每日10 mg(44%)。停药的最常见原因是急性移植物抗宿主病(GVHD)(37%)和疾病进展(37%)。从开始使用LEN起,III至IV级急性GVHD的累积发生率为17%。维持治疗开始后18个月时的结果为:MM进展28%;移植相关死亡率11%;无进展生存率和总生存率分别为63%和78%。alloHCT后使用LEN在较低剂量下是可行的,尽管它与38%的急性GVHD发生率相关。在这个高危MM人群中观察到的生存结果值得对这种方法进行进一步研究。

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