Wu Aaron, Graf Solomon A, Burwick Nicholas, Grim Jonathan E, Dong Zhao Ming, Richard Robert E, Chauncey Thomas R
Department of Hospital and Specialty Medicine, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA.
Division of Oncology, University of Washington Medicine, Seattle, WA, USA.
Blood Res. 2020 Mar;55(1):57-61. doi: 10.5045/br.2020.55.1.57. Epub 2020 Mar 30.
Autologous stem cell transplantation (autoSCT) can extend remission of mantle cell lymphoma (MCL), but the management of subsequent relapse is challenging.
We examined consecutive patients with MCL who underwent autoSCT at Veterans Affairs Puget Sound Health Care System between 2009 and 2017 (N=37).
Ten patients experienced disease progression after autoSCT and were included in this analysis. Median progression free survival after autoSCT was 1.8 years (range, 0.3-7.1) and median overall survival after progression was only 0.7 years (range, 0.1 to not reached). The 3 patients who survived more than 1 year after progression were treated with ibrutinib.
Our findings suggest that ibrutinib can achieve relatively prolonged control of MCL progressing after autoSCT.
自体干细胞移植(autoSCT)可延长套细胞淋巴瘤(MCL)的缓解期,但后续复发的管理具有挑战性。
我们研究了2009年至2017年间在普吉特海湾退伍军人事务医疗保健系统接受autoSCT的连续性MCL患者(N = 37)。
10例患者在autoSCT后出现疾病进展,并纳入本分析。autoSCT后的无进展生存期(PFS)中位数为1.8年(范围0.3 - 7.1年),进展后的总生存期(OS)中位数仅为0.7年(范围0.1年至未达到)。3例进展后存活超过1年的患者接受了伊布替尼治疗。
我们的研究结果表明,伊布替尼可实现对autoSCT后进展的MCL的相对长期控制。