Hosing C, Bassett R, Dabaja B, Talpur R, Alousi A, Ciurea S, Popat U, Qazilbash M, Shpall E J, Oki Y, Nieto Y, Pinnix C, Fanale M, Maadani F, Donato M, Champlin R, Duvic M
Department of Stem Cell Transplantation and Cellular Therapy
Department of Biostatistics.
Ann Oncol. 2015 Dec;26(12):2490-5. doi: 10.1093/annonc/mdv473. Epub 2015 Sep 28.
Cutaneous T-cell lymphomas (CTCLs) and its common variants mycosis fungoides (MF) and leukemic Sézary syndrome (SS) are rare extranodal non-Hodgkin's lymphomas. Patients who present with advanced disease and large-cell transformation (LCT) are incurable with standard treatments. In this article, we report the largest single-center experience with allogeneic stem-cell transplantation (SCT) for advanced CTCL.
This is a prospective case series of 47 CTCL patients who underwent allogeneic SCT after failure of standard therapy between July 2001 and September 2013. The Kaplan-Meier method was used to estimate overall survival (OS) and progression-free survival (PFS) curves. The method of Fine and Gray was used to fit regression models to the same covariates for these cumulative incidence data.
The Kaplan-Meier estimates of OS and PFS at 4 years were 51% and 26%, respectively. There was no statistical difference in the OS in patients who had MF alone, SS, MF with LCT, or SS with LCT. PFS at 4 years was superior in patients who had SS versus those who did not (52.4% versus 9.9%; P = 0.02). The cumulative incidences of grade 2-4 acute graft-versus-host disease (GVHD) and chronic GVHD were 40% and 28%, respectively. The cumulative nonrelapse mortality rate was 16.7% at 2 years.
Allogeneic SCT may result in long-term remissions in a subset of patients with advanced CTCL. Although post-SCT relapse rates are high, many patients respond to immunomodulation and achieve durable remissions.
NCT00506129.
皮肤T细胞淋巴瘤(CTCL)及其常见变异型蕈样肉芽肿(MF)和白血病性Sezary综合征(SS)是罕见的结外非霍奇金淋巴瘤。出现晚期疾病和大细胞转化(LCT)的患者无法通过标准治疗治愈。在本文中,我们报告了同种异体干细胞移植(SCT)治疗晚期CTCL的最大单中心经验。
这是一项前瞻性病例系列研究,纳入了2001年7月至2013年9月间47例标准治疗失败后接受同种异体SCT的CTCL患者。采用Kaplan-Meier方法估计总生存期(OS)和无进展生存期(PFS)曲线。使用Fine和Gray方法对这些累积发病率数据的相同协变量拟合回归模型。
4年时OS和PFS的Kaplan-Meier估计值分别为51%和26%。单纯MF、SS、MF合并LCT或SS合并LCT的患者在OS方面无统计学差异。4年时,SS患者的PFS优于非SS患者(52.4%对9.9%;P = 0.02)。2-4级急性移植物抗宿主病(GVHD)和慢性GVHD的累积发病率分别为40%和28%。2年时累积非复发死亡率为16.7%。
同种异体SCT可能使一部分晚期CTCL患者获得长期缓解。虽然SCT后复发率较高,但许多患者对免疫调节有反应并实现持久缓解。
NCT00506129。