首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Permanent Impairment-Free, Relapse-Free Survival: A Novel Composite Endpoint to Evaluate Long-Term Success in Allogeneic Transplantation
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Permanent Impairment-Free, Relapse-Free Survival: A Novel Composite Endpoint to Evaluate Long-Term Success in Allogeneic Transplantation

机译:永久性无损,无复发生存:一种新型复合终点,以评估同种异体移植的长期成功

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Permanent impairment (PI) of vital organs is one of the transplantation-related health problems affecting the quality of life and morbidity even in patients who do not develop graft-versus-host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (allo-HCT), but no data are available on PI of multiple organs. This retrospective study aimed to estimate a novel composite endpoint of PI-free, relapse-free survival (PIRFS) in 164 allo-HCT recipients. We defined PI as >26% to 30% impairment of the whole person in 6 vital organs using the whole person impairment rating. Conventional GVHD-free/relapse-free survival (GRFS) and PIRFS at 5 years were 33.8% (95% confidence interval [CI], 26.5% to 41.3%) and 40.6% (95% CI, 32.6% to 48.4%), respectively. In the whole cohort, PIRFS was higher than GRFS at any time after allo-HCT. However, PIRFS was lower than GRFS after day 397 post-transplantation in patients who underwent umbilical cord blood transplantation (UCBT). In UCBT recipients, 5-year GRFS and PIRFS were 47.6% (95% CI, 34.3% to 59.7%) and 39.2% (95% CI, 26.6% to 51.5%), respectively. The cumulative incidence of PI after 5 years was 20.9% (95% CI, 13.7% to 29.0%) in patients surviving for >= 6 months without relapse. The multivariate analysis revealed that high disease risk (hazard ratio [HR], 1.91; 95% CI, 1.26 to 2.88; P < .01) and Karnofsky Performance Status score <= 90% at transplantation (HR, 1.73; 95% CI, 1.14 to 2.63; P = .01) were correlated with the lower PIRFS, whereas UCBT (HR, 2.35; 95% CI, 1.11 to 4.99; P = .03), grade III-IV acute GVHD by day 180 (HR, 3.59; 95% CI, 1.04 to 12.4; P = .04), and thrombotic microangiopathy by day 180 (HR, 2.74; 95% CI, 1.10 to 6.87; P = .03) were significantly correlated with a higher incidence of PI. More than 20% of long-term survivors had PI. Our data suggest that PIRFS is a useful endpoint for assessing long-term transplantation success from a different perspective than has been established previously. (C) 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
机译:重要的器官的永久性损伤(PI)是在同种异体造血干细胞移植(Allo-Hct)后没有发展移植物与宿主疾病(GVHD)的患者中,即使在不开发移植物与宿主病(GVHD)的患者中,也是影响生活质量和发病率的移植相关健康问题之一),但多个器官的PI上没有任何数据。这种回顾性研究旨在估算164个Allo-HCT受体中的无皮,无复发存活(PIRFS)的新型复合终点。我们使用整个人的减值评级定义了6个重要机构在6个重要机构中的PI标准损害。 5岁的常规GVHD /复发存活(GRF)和PIRFS为33.8%(95%置信区间[CI],26.5%至41.3%)和40.6%(95%CI,32.6%至48.4%),分别。在整个队列中,PIRFS在Allo-Hct后的任何时间都高于GRF。然而,在接受脐带血液移植(UCBT)的患者后,PIRFS在移植后的第397天后低于GRF。在UCBT受者中,5年的GRF和PIRFS分别为47.6%(95%CI,34.3%至59.7%)和39.2%(95%CI,26.6%至51.5%)。 5年后Pi的累积发病率为20.9%(95%CI,13.7%至29.0%),患者存活> = 6个月而不会复发。多变量分析显示出高疾病风险(危害比[HR],1.91; 95%CI,1.26至2.88; P <.01)和Karnofsky性能状态得分<= 90%,在移植下(HR,1.73; 95%CI, 1.14至2.63; p = .01)与下部PiRF相关,而UCBT(HR,2.35; 95%CI,1.11至4.99; P = .03),III-IV级急性GVHD在180天(HR,3.59 ; 95%CI,1.04至12.4; p = .04),并在180天(HR,2.74; 95%CI,1.10至6.87; p = .03)与pi的发病率显着相关。超过20%的长期幸存者有PI。我们的数据表明,PIRFS是一种有用的端点,用于评估不同的角度而不是先前建立的长期移植成功。 (c)2020年美国移植和细胞疗法协会。 elsevier公司发布

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