PO.CL09.02 · 临床研究

利用大型国家癌症数据库评估累及肝脏和胃肠道的IV期PTCL, NOS

Evaluation of stage IV PTCL, NOS of the liver and gastrointestinal tract using a large national cancer database

海报缩略图:利用大型国家癌症数据库评估累及肝脏和胃肠道的IV期PTCL, NOS
编号 6635 展板 4 时间 4/21 02:00–05:00 区域 Section 47 主讲 Olivia Davis, MD
分会场 Real World Data to Provide Real World Evidence
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作者与单位 Authors & Affiliations

Olivia Davis1, Taha Al-Juhaishi2, Ryan Wilcox3

1Department of Internal Medicine, University of Michigan, Ann Arbor, MI,2Department of Internal Medicine, Division of Hematology/Oncology, University of Oklahoma, OU Health, Oklahoma City, OK,3Department of Internal Medicine, Division of Hematology/Oncology, University of Michigan, Ann Arbor, MI

摘要 Abstract

中文摘要
引言:外周T细胞淋巴瘤,非特指型(PTCL, NOS)是一组异质性PTCL,结外受累常见且预后差。既往研究提示,原发部位可能影响早期PTCL, NOS的总生存期(OS),胃肠道/泌尿生殖系统受累者结局更差。关于原发部位在晚期疾病中的作用以及离散性胃肠器官受累的影响,目前知之甚少。本研究的目的是利用国家癌症数据库探究伴结外受累的IV期PTCL, NOS的结局。 方法:从监测、流行病学和最终结果(SEER)数据库中提取2000年至2015年间诊断为PTCL, NOS个体的患者及疾病特征。分离出结外IV期PTCL, NOS患者并纳入最终分析,以反映广泛结外受累的病例。根据识别出的最常见原发部位,将原发部位分为11个不同类别。我们主要关注的原发部位为肝脏和管腔胃肠道,但也分析了其他原发部位,以脾脏作为对照组。采用汇总统计分析患者和疾病特征。生存分析采用Kaplan-Meier法和Cox比例风险模型。为每个病例确定治疗状态,并针对每个原发部位比较化疗组与非化疗组之间的生存。 结果:最终分析共纳入464例患者。中位年龄为63.0岁。多数患者为非西班牙裔白人(60.8%)或男性(62.3%)。13例(2.8%)累及肝脏原发病灶,70例(15.1%)累及胃肠道。累及肝脏的IV期PTCL, NOS中位OS为1个月[95% CI(0-4)]。累及胃肠道的IV期PTCL, NOS中位OS为4个月[95% CI(3-5)]。肝脏原发病灶与更差的淋巴瘤特异性生存相关[HR=2.400,95% CI(1.081-5.328);p值=0.0314]。胃肠道原发病灶与更差的淋巴瘤特异性生存[HR=2.090,95% CI(1.220-3.579);p值=0.0073]和总生存[HR=1.797,95% CI(1.121-2.881);p值=0.0149]相关。累及肝脏的PTCL, NOS治疗组间在总生存或疾病特异性生存方面未检测到统计学显著差异[HR=0.780,95% CI(0.185-3.287);p值=0.7354]。 结论:累及管腔胃肠道的IV期PTCL, NOS与更差的OS和疾病特异性生存相关。累及肝脏的IV期PTCL, NOS与更差的疾病特异性生存相关,可能被视为化疗耐药区室。
查看英文原文 English abstract
Introduction: Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) is a heterogeneous group of PTCL for which extranodal involvement is common and outcomes are poor. Previous research has suggested that primary disease site may impact overall survival (OS) for early-stage PTCL, NOS with worse outcomes for patients with gastrointestinal/genitourinary involvement. Little is known about the role of primary disease site in advanced stage disease and the impact of discrete gastrointestinal organ involvement. The purpose of this study was to investigate outcomes for stage IV PTCL, NOS with extranodal involvement using a national cancer database. Methods: Patient and disease characteristics for individuals diagnosed with PTCL, NOS between 2000 and 2015 were extracted from the Surveillance, Epidemiology, and End Results (SEER) database. Patients with extranodal stage IV PTCL, NOS were isolated and included in the final analysis to reflect cases of extensive extranodal involvement. Primary disease sites were grouped into 11 distinct categories based on the most common primary sites identified. Our main primary disease sites of interest were liver and luminal GI tract, but other primary disease sites were analyzed as well with spleen serving as the comparison group. Patient and disease characteristics were analyzed using summary statistics. Survival analyses were performed using the Kaplan-Meier method and Cox proportional hazards models. Treatment status was identified for each case, and survival was compared between chemotherapy and non-chemotherapy groups for each primary disease site. Results: A total of 464 patients were included in the final analysis. Median age was 63.0 years. Most patients were non-Hispanic white (60.8%) or male (62.3%). Thirteen cases (2.8%) involved primary disease of the liver while 70 cases (15.1%) involved the GI tract. Median OS for stage IV PTCL, NOS involving the liver was 1 month (95% CI (0-4)]. Median OS for stage IV PTCL, NOS of the GI tract was 4 months [95% CI (3-5)]. Primary disease of the liver was associated with worse lymphoma-specific survival [HR=2.400, 95% CI (1.081-5.328); p-value=0.0314]. Primary disease of the GI tract was associated with worse lymphoma-specific survival [HR=2.090, 95% CI (1.220-3.579); p-value=0.0073] and overall survival [HR=1.797, 95% CI (1.121-2.881); p-value=0.0149]. No statistically significant difference in overall survival or disease-specific survival was detected between treatment groups for PTCL, NOS of the liver [HR=0.780, 95% CI (0.185-3.287); p-value=0.7354]. Conclusions: Stage IV PTCL, NOS of the luminal GI tract was associated with worse OS and disease-specific survival. Stage IV PTCL, NOS of the liver was associated with worse disease-specific survival and may be considered a chemotherapy-resistant compartment.
利益披露 Disclosure
O. Davis, None.. T. Al-Juhaishi, None.. R. Wilcox, None.

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