Long-Term Survival Analysis of Neoadjuvant Chemoradiotherapy Versus Adjuvant Chemoradiotherapy for Locally Advanced Low Rectal Cancer

IF 2.9 2区 医学 Q2 ONCOLOGY
Cancer Medicine Pub Date : 2025-07-25 DOI:10.1002/cam4.71042
Siyuan Chen, Ruiyan Wu, Juefeng Wan, Yun Xu, Yaqi Wang, Zhiyuan Zhang, Lili Huang, Yujun Liu, Yingxuan Lin, Luoxi He, Yun Deng, Fan Xia, Ye Xu, Zhen Zhang, Hongtu Zheng
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Abstract

Purpose

To compare the long-term survival of patients with locally advanced low rectal cancer (LALRC), receiving neoadjuvant chemoradiotherapy (NCRT) versus adjuvant chemoradiotherapy (ACRT).

Methods and Materials

This retrospective observational study included 1169 patients with LALRC (Stage II/III disease located ≤ 5 cm from the anal verge) who underwent diagnosis and treatment at Fudan University Shanghai Cancer Center from February 2006 to March 2021. In Stage II/III low rectal cancer patients, one-to-one matched pairs were created from the ACRT and NCRT groups using propensity score matching (PSM) based on baseline characteristics. OS and DFS were evaluated using the Kaplan–Meier method alongside the univariate Cox regression model.

Results

In Stage II patients, 65 received ACRT and 107 received NCRT. For Stage III, 282 received ACRT and 715 received NCRT. After PSM, 45 paired Stage II patients and 243 paired Stage III patients were selected. In Stage II patients, there was no significant difference in OS and DFS between the groups. For Stage III, the 5- and 10-year OS rates were 79.61% and 77.67% in the NCRT group, compared to 61.08% and 44.57% in the ACRT group (p < 0.001). The 5- and 10-year DFS rates were 69.93% and 65.26% in the NCRT group, versus 48.07% and 40.77% in the ACRT group (p < 0.001). Additionally, in Stage III patients, NCRT was associated with a significant reduction in the risk of death and recurrence compared to ACRT (OS: HR = 0.47, p = 0.0001; DFS: HR = 0.55, p = 0.0001).

Conclusion

For patients with Stage III low rectal cancer, NCRT significantly improved the long-term DFS rate and OS rate, in comparison to adjuvant chemoradiotherapy.

Abstract Image

局部晚期低位直肠癌新辅助放化疗与辅助放化疗的长期生存分析
目的比较局部晚期低位直肠癌(LALRC)患者接受新辅助放化疗(NCRT)与辅助放化疗(ACRT)的长期生存率。方法和材料本回顾性观察性研究纳入了2006年2月至2021年3月在复旦大学上海肿瘤中心诊断和治疗的1169例LALRC (II/III期疾病位于肛门边缘≤5 cm)患者。在II/III期低位直肠癌患者中,使用基于基线特征的倾向评分匹配(PSM),从ACRT组和NCRT组中创建一对一匹配对。采用Kaplan-Meier法和单变量Cox回归模型评估OS和DFS。结果二期患者中,ACRT治疗65例,NCRT治疗107例。第三阶段,282人接受ACRT, 715人接受NCRT。经PSM后,选择配对II期患者45例,配对III期患者243例。在II期患者中,两组间OS和DFS无显著差异。对于III期,NCRT组的5年和10年OS率分别为79.61%和77.67%,而ACRT组为61.08%和44.57% (p < 0.001)。NCRT组5年和10年DFS分别为69.93%和65.26%,而ACRT组为48.07%和40.77% (p < 0.001)。此外,在III期患者中,与ACRT相比,NCRT与死亡和复发风险的显著降低相关(OS: HR = 0.47, p = 0.0001;DFS: HR = 0.55, p = 0.0001)。结论对于III期低位直肠癌患者,与辅助放化疗相比,NCRT显著提高了长期DFS率和OS率。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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