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造血干细胞移植对复发或难治性套细胞淋巴瘤患者的影响。

Impact of hematopoietic stem cell transplantation in patients with relapsed or refractory mantle cell lymphoma.

机构信息

Department of Hematology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, 1-8-1 Jigyohama, Chuo-Ku, Fukuoka, 810-8563, Japan.

Department of Internal Medicine, The University of New Mexico, Albuquerque, NM, USA.

出版信息

Ann Hematol. 2018 Aug;97(8):1445-1452. doi: 10.1007/s00277-018-3318-5. Epub 2018 Apr 2.

Abstract

Rituximab has been shown to improve outcomes in patients with B-cell lymphoma. However, patients with relapsed or refractory (R/R) mantle cell lymphoma (MCL) still have a poor prognosis, and the choice between high-dose therapy with autologous hematopoietic cell transplantation (HCT) and allogeneic HCT remains controversial in these patients. We retrospectively analyzed the risk factors for outcomes in 162 R/R MCL patients who received autologous (n = 111) or allogeneic (n = 51) HCT between 2004 and 2014. The median overall survival (OS) rates were 48 and 65 months in the autologous and allogeneic HCT groups, respectively (P = 0.20). Significant risk factors for overall survival in R/R MCL patients after autologous HCT were > 60 years of age at HCT (P = 0.017), higher score of HCT-specific comorbidity index at HCT (P = 0.033), and receiving MCEC (ranimustine + carboplatin + etoposide + cyclophosphamide) regimen (P = 0.017), while higher performance status at HCT (P = 0.011) and longer interval from diagnosis to HCT (P = 0.0054) were risk factors after allogeneic HCT. Strategies that carefully select R/R MCL patients for autologous HCT may allow the identification of individuals suitable for allogeneic HCT.

摘要

利妥昔单抗已被证明可改善 B 细胞淋巴瘤患者的预后。然而,复发或难治性(R/R)套细胞淋巴瘤(MCL)患者的预后仍然较差,在这些患者中,高剂量治疗联合自体造血细胞移植(HCT)与异基因 HCT 之间的选择仍存在争议。我们回顾性分析了 162 例 R/R MCL 患者在 2004 年至 2014 年期间接受自体(n=111)或异基因(n=51)HCT 的结果的危险因素。自体和异基因 HCT 组的中位总生存期(OS)分别为 48 个月和 65 个月(P=0.20)。R/R MCL 患者自体 HCT 后总生存的显著危险因素为 HCT 时年龄>60 岁(P=0.017)、HCT 时 HCT 特异性合并症指数评分较高(P=0.033)和接受 MCEC(喷司他丁+卡铂+依托泊苷+环磷酰胺)方案(P=0.017),而异基因 HCT 后较高的 HCT 表现状态(P=0.011)和从诊断到 HCT 的间隔时间较长(P=0.0054)是危险因素。仔细选择适合自体 HCT 的 R/R MCL 患者的策略可能有助于确定适合异基因 HCT 的个体。

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