淋巴细胞减少是直肠腺癌患者接受长期放化疗的一个不良预后因素。

Radiation oncology journal Pub Date : 2024-12-01 Epub Date: 2024-12-23 DOI:10.3857/roj.2024.00052
Ioannis M Koukourakis, Ioannis Georgakopoulos, Dimitra Desse, Dina Tiniakos, Vassilios Kouloulias, Anna Zygogianni
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引用次数: 0

摘要

目的:新辅助放疗(RT)或放化疗(CRT)是局部晚期直肠腺癌的标准治疗方法。最近出现的关于术前免疫治疗作为错配修复缺陷直肠癌的有效治疗方式的数据表明,免疫系统在肿瘤根除中起着重要作用。虽然RT已被证明可以刺激抗肿瘤免疫,但它也会导致大量淋巴细胞减少,阻碍免疫反应的效果。材料与方法:回顾性分析我科33例接受过CRT治疗的直肠腺癌患者,旨在探讨CRT对外周血淋巴细胞计数(LC)的影响,以及CRT诱导的淋巴细胞减少对患者肿瘤反应及预后的潜在影响。结果:CRT后患者LC降低,治疗前后中位值分别为2184 /μL、517/μL,差异有统计学意义;P < 0.001)。虽然ypt分期、ypN状态与LC无相关性,但肿瘤消退等级差与LC较低显著相关(p = 0.036)。此外,淋巴细胞减少与较差的远端无转移生存相关(p = 0.003)。crt后LC高于518/μL的患者中有0%发生远处转移,而LC值较低的患者中有44.5%发生远处转移。结论:虽然需要进一步研究,但考虑到本研究分析的患者数量有限,淋巴细胞减少成为直肠癌患者在新辅助CRT治疗过程中面临的一个重要不良事件,并对肿瘤反应和预后产生影响。CRT过程中免疫系统的保护已成为临床研究的重要目标。
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Lymphopenia is an adverse prognostic factor in rectal adenocarcinoma patients receiving long-course chemoradiotherapy.

Purpose: Neoadjuvant radiotherapy (RT) or chemoradiotherapy (CRT) is the standard treatment for locally advanced rectal adenocarcinoma. The recent emerging data on preoperative immunotherapy as an effective therapeutic modality for mismatch repair deficient rectal carcinomas suggests that the immune system plays a significant role in tumor eradication. Although RT has been shown to stimulate anti-tumor immunity, it also leads to substantial lymphopenia, hindering the effect of immune response.

Materials and methods: We retrospectively analyzed 33 rectal adenocarcinoma patients who underwent CRT in our department, aiming to identify the effects of CRT on the peripheral blood lymphocyte counts (LC) and the potential impact of CRT-induced lymphopenia on tumor response and prognosis of patients.

Results: A statistically significant decrease in the LC of patients was observed after CRT (median values of 2,184/μL and 517/μL before and after treatment, respectively; p < 0.001). While no correlation between ypT-stage, ypN status, and LC was found, poor tumor regression grade was significantly associated with lower LC (p = 0.036). Moreover, lymphopenia was associated with poorer distant metastasis-free survival (p = 0.003). Distant metastases were documented in 0% of patients with post-CRT LC above 518/μL vs. 44.5% of patients with lower LC values.

Conclusion: Although further investigation is demanded, given the limited number of patients analyzed in the study, lymphopenia emerges as a significant adverse event that rectal adenocarcinoma patients face during treatment with neoadjuvant CRT, with subsequent implications on tumor response and prognosis. Protection of the immune system during CRT emerges as an important target for clinical research.

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