严重淋巴细胞减少预示着接受新辅助放化疗的直肠癌患者较差的生存率。

IF 2.6 4区 医学 Q3 ONCOLOGY
Daniel W Kim, Grace Lee, Elise M Cai, David P Ryan, Aparna R Parikh, Jill N Allen, Bruce J Giantonio, David L Berger, Hiroko Kunitake, Rocco Ricciardi, James C Cusack, Hannah J Roberts, Theodore S Hong, Jennifer Y Wo
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引用次数: 0

摘要

目的:放化疗引起的淋巴细胞减少症在多发性实体恶性肿瘤中很常见,并与较差的生存率相关。然而,直肠癌放化疗相关淋巴细胞减少与生存结果之间的关系尚不清楚。本研究的目的是评估淋巴细胞减少症及其预测因素对接受新辅助放化疗的直肠癌患者的预后影响。方法:这项单机构回顾性研究的纳入标准如下:(1)经活检证实的直肠腺癌诊断,(2)手术后接受新辅助放化疗,(3)放化疗前和12周内的绝对淋巴细胞计数。一般来说,放化疗包括5-氟尿嘧啶或卡培他滨和放疗,放疗剂量为50.4 Gy,超过28个分数。根据不良事件通用术语标准5.0版对淋巴细胞减少症进行分级。主要研究变量是放化疗后12周内的绝对淋巴细胞计数最低点,根据结果进行二分类:共有193例患者被确定,中位随访时间为68个月。总临床分期为2 / 21%,3 / 76%。整个队列的中位基线淋巴细胞计数为1700/μL。110名患者(57%)经历了与放化疗相关的严重淋巴细胞减少症。病理完全缓解率为21%;83%接受了辅助化疗。较低的基线淋巴细胞计数与放化疗相关的严重淋巴细胞减少的风险增加显著相关(优势比,1.71)。在多变量Cox回归分析中,放化疗相关的严重淋巴细胞减少与较差的无病生存(风险比为2.64)和总生存(风险比为4.32)显著相关。在经历和未经历严重淋巴细胞减少的队列中,5年总生存率分别为79%和92%,5年无病生存率为70%和86%。讨论:放化疗引起的淋巴细胞减少是常见的,是直肠癌较差生存的预后标志。对高危患者进行更密切的观察和修改治疗方法可能是减轻治疗相关性淋巴细胞减少症的潜在途径。我们的研究结果还表明,宿主免疫在直肠癌预后中的重要作用,并支持未来研究减少治疗性淋巴细胞减少的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe Lymphopenia Predicts Poorer Survival in Patients With Rectal Cancer Undergoing Neoadjuvant Chemoradiation.

Purpose: Chemoradiation-induced lymphopenia is common and associated with poorer survival in multiple solid malignancies. However, the association between chemoradiation-related lymphopenia and survival outcomes in rectal cancer is yet unclear. The objective of this study was to evaluate the prognostic impact of lymphopenia and its predictors in patients with rectal cancer undergoing neoadjuvant chemoradiation.

Methods: The inclusion criteria for this single-institution retrospective study were as follows: (1) biopsy-proven diagnosis of rectal adenocarcinoma, (2) receipt of neoadjuvant chemoradiation followed by surgery, and (3) absolute lymphocyte count available prior to and within 12 weeks of chemoradiation. In general, chemoradiation consisted of 5-fluorouracil or capecitabine and radiotherapy with 50.4 Gy over 28 fractions. Lymphopenia was graded according to the Common Terminology Criteria for Adverse Events version 5.0. The primary variable of interest was absolute lymphocyte count nadir within 12 weeks of chemoradiation, dichotomized by <500/μL (grade 3 or worse lymphopenia). The primary endpoint was overall survival. Cox modeling and Kaplan-Meier methods were used to perform survival analyses.

Results: A total of 193 patients were identified with a median follow-up of 68 months. Overall clinical stage was 2 in 21% and 3 in 76%. Median baseline lymphocyte count for the entire cohort was 1700/μL. One hundred ten patients (57%) experienced chemoradiation-related severe lymphopenia. Pathologic complete response rate was 21%; 83% received adjuvant chemotherapy. Lower baseline lymphocyte count was significantly associated with increased risk for chemoradiation-related severe lymphopenia (odds ratio, 1.71). On multivariable Cox regression analysis, chemoradiation-related severe lymphopenia was significantly associated with worse disease-free survival (hazard ratio, 2.64) and overall survival (hazard ratio, 4.32). Five-year overall survival was 79% versus 92%, and 5-year disease-free survival was 70% versus 86% in the cohort that experienced versus did not experience severe lymphopenia, respectively.

Discussion: Chemoradiation-induced lymphopenia is common and a prognostic marker of poorer survival in rectal cancer. Closer observation in high-risk patients and treatment modifications may be potential approaches to mitigating treatment-related lymphopenia. Our findings also suggest an important role of the host immunity in rectal cancer outcomes and support future studies investigating ways to reduce treatment-induced lymphopenia.

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来源期刊
Cancer journal
Cancer journal 医学-肿瘤学
CiteScore
3.90
自引率
0.00%
发文量
102
审稿时长
7.5 months
期刊介绍: The Cancer Journal: The Journal of Principles & Practice of Oncology provides an integrated view of modern oncology across all disciplines. The Journal publishes original research and reviews, and keeps readers current on content published in the book Cancer: Principles & Practice of Oncology.
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