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成人实体器官移植受者移植后淋巴细胞增殖性疾病生存的预后分析

Prognostic analysis for survival in adult solid organ transplant recipients with post-transplantation lymphoproliferative disorders.

作者信息

Ghobrial Irene M, Habermann Thomas M, Maurer Matthew J, Geyer Susan M, Ristow Kay M, Larson Timothy S, Walker Randall C, Ansell Stephen M, Macon William R, Gores Gregory G, Stegall Mark D, McGregor Christopher G

机构信息

Division of Hematology, Department of Internal Medicine, Mayo Clinic and Mayo Foundation, 200 First St, SW, Rochester, MN 55905, USA.

出版信息

J Clin Oncol. 2005 Oct 20;23(30):7574-82. doi: 10.1200/JCO.2005.01.0934. Epub 2005 Sep 26.

Abstract

PURPOSE

The objective of this study was to determine prognostic factors for overall survival in patients with post-transplantation lymphoproliferative disorders (PTLDs).

PATIENTS AND METHODS

This study focused on the 107 adult solid organ transplantation patients who were diagnosed with PTLDs at Mayo Clinic (Rochester, MN) between December 1970 and May 2003.

RESULTS

The median age at the time of diagnosis was 48 years (range, 15 to 75 years). Extranodal disease including grafted organ involvement was present in 85 patients (80%). The graft organ was involved in 30 patients (28%). At the time of these analyses, 62 patients (58%) had died. The median survival for the entire cohort was 31.5 months (95% CI, 10.7 to 72.5 months). The median follow-up of living patients was 51.8 months (range, 5.6 to 202.6 months). In univariate analyses for overall survival from the time of PTLD diagnosis, the following poor prognostic factors were identified: poor performance status with Eastern Cooperative Oncology Group levels 3 and 4 (P < .0001), grafted organ involvement (P = .0005), the presence of one or more extranodal sites (P = .005), both nodal and extranodal disease (P = .002), high International Prognostic Index (P = .006), advanced stage (P = .001), and elevated lactate dehydrogenase (P = .03). A final multivariable model for survival was constructed using three factors: poor performance status (3 to 4), monomorphic disease, and graft organ involvement.

CONCLUSION

A prognostic model has been developed for PTLD patients using one center's 30 years of experience. We propose additional confirmation and validation of these prognostic factors in larger prospective studies.

摘要

目的

本研究的目的是确定移植后淋巴细胞增生性疾病(PTLD)患者总生存的预后因素。

患者与方法

本研究聚焦于1970年12月至2003年5月间在梅奥诊所(明尼苏达州罗切斯特)被诊断为PTLD的107例成人实体器官移植患者。

结果

诊断时的中位年龄为48岁(范围15至75岁)。85例患者(80%)存在结外病变,包括移植器官受累。30例患者(28%)的移植器官受累。在进行这些分析时,62例患者(58%)已经死亡。整个队列的中位生存期为31.5个月(95%可信区间,10.7至72.5个月)。存活患者的中位随访时间为51.8个月(范围5.6至202.6个月)。在从PTLD诊断时起的总生存单因素分析中,确定了以下不良预后因素:东部肿瘤协作组(ECOG)3级和4级的不良表现状态(P <.0001)、移植器官受累(P =.0005)、存在一个或多个结外部位(P =.005)、同时存在淋巴结和结外病变(P =.002)、高国际预后指数(P =.006)、晚期(P =.001)以及乳酸脱氢酶升高(P =.03)。使用三个因素构建了最终的生存多变量模型:不良表现状态(3至4级)、单形性疾病和移植器官受累。

结论

利用一个中心30年的经验为PTLD患者开发了一种预后模型。我们建议在更大规模的前瞻性研究中对这些预后因素进行进一步的确认和验证。

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