文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

荷兰临床淋巴结阴性但病理淋巴结阳性直肠癌患者的辅助化疗:一项回顾性分析。

Adjuvant chemotherapy in patients with clinically node-negative but pathologically node-positive rectal cancer in the Netherlands: A retrospective analysis.

机构信息

Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, the Netherlands; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, the Netherlands.

Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

出版信息

Eur J Cancer. 2024 Jan;197:113466. doi: 10.1016/j.ejca.2023.113466. Epub 2023 Dec 2.


DOI:10.1016/j.ejca.2023.113466
PMID:38061213
Abstract

INTRODUCTION: Accurate clinical staging of rectal cancer is hampered by suboptimal sensitivity of MRI in the detection of regional lymph node metastases. Consequently, some patients may be understaged and have been withheld neoadjuvant (chemo)radiotherapy in retrospect. Although Dutch guidelines do not advocate adjuvant chemotherapy (ACT) in rectal cancer, some of these clinically understaged patients receive ACT according to local policy. We aim to assess the benefit of ACT in these patients. METHODS: Population-based data from patients with clinically node-negative (cN0) but pathologically node-positive (pN+) rectal cancer that underwent total mesorectal excision (TME) without neoadjuvant treatment between 2008 and 2018 were obtained from the Netherlands Cancer Registry. Missing data were handled by multiple imputation. Stabilised inverse probability treatment weighting (sIPTW) was used to balance clinical characteristics. Overall survival (OS) was compared in ACT and non-ACT patients. RESULTS: Of 34,724 patients, 13,861 had cN0 disease of whom 3016 were pN+ (21.8%). 1466 (48.6%) of these patients underwent upfront TME and were included. Median follow-up was 84 months (95% confidence interval [CI] 76-97) versus 79 months (95% CI 77-81) in patients that did (n = 290, 19.8%) and did not (n = 1176, 80.2%) receive ACT, respectively. After sIPTW adjustment, ACT was associated with improved OS (hazard ratio 0.70; 95% CI 0.49-0.99; p = 0.04). The estimated 5-year OS rate was 74.2% versus 65.3%, respectively. CONCLUSION: In this population-based cohort of patients with cN0 but pN+ rectal cancer who underwent upfront TME, ACT was associated with a significant OS benefit. These data support to discuss ACT in this population.

摘要

介绍:由于 MRI 在检测局部淋巴结转移方面的敏感性不足,直肠 癌的准确临床分期受到阻碍。因此,一些患者可能被低估分期,并且回顾性地被排除在新辅助(化疗)放疗之外。尽管荷兰指南不主张在直肠 癌中使用辅助化疗(ACT),但根据当地政策,其中一些临床低估分期的患者会接受 ACT。我们旨在评估这些患者接受 ACT 的获益。

方法:从荷兰癌症登记处获得了 2008 年至 2018 年间接受全直肠系膜切除术(TME)且未经新辅助治疗的临床淋巴结阴性(cN0)但病理淋巴结阳性(pN+)直肠 癌患者的基于人群的数据。通过多次插补处理缺失数据。使用稳定逆概率治疗加权(sIPTW)来平衡临床特征。比较 ACT 和非 ACT 患者的总生存(OS)。

结果:在 34724 名患者中,有 13861 名患者患有 cN0 疾病,其中 3016 名患者为 pN+(21.8%)。其中 1466 名患者(48.6%)接受了 upfront TME 并被纳入研究。中位随访时间为 84 个月(95%置信区间 [CI] 76-97),与未接受 ACT(n=290,19.8%)和接受 ACT(n=1176,80.2%)的患者相比,分别为 79 个月(95% CI 77-81)。经过 sIPTW 调整后,ACT 与 OS 改善相关(风险比 0.70;95% CI 0.49-0.99;p=0.04)。估计的 5 年 OS 率分别为 74.2%和 65.3%。

结论:在接受 upfront TME 的 cN0 但 pN+直肠 癌患者的这一基于人群的队列中,ACT 与显著的 OS 获益相关。这些数据支持在该人群中讨论 ACT。

相似文献

[1]
Adjuvant chemotherapy in patients with clinically node-negative but pathologically node-positive rectal cancer in the Netherlands: A retrospective analysis.

Eur J Cancer. 2024-1

[2]
Oncologic benefit of adjuvant chemotherapy for locally advanced rectal cancer after neoadjuvant chemoradiotherapy and curative surgery with selective lateral pelvic lymph node dissection: An international retrospective cohort study.

Eur J Surg Oncol. 2022-7

[3]
Upfront radical surgery with total mesorectal excision followed by adjuvant FOLFOX chemotherapy for locally advanced rectal cancer (TME-FOLFOX): an open-label, multicenter, phase II randomized controlled trial.

Trials. 2020-4-7

[4]
Adjuvant chemotherapy for rectal cancer patients treated with preoperative (chemo)radiotherapy and total mesorectal excision: a Dutch Colorectal Cancer Group (DCCG) randomized phase III trial.

Ann Oncol. 2014-12-5

[5]
Local recurrences in western low rectal cancer patients treated with or without lateral lymph node dissection after neoadjuvant (chemo)radiotherapy: An international multi-centre comparative study.

Eur J Surg Oncol. 2021-9

[6]
Short-course radiotherapy followed by chemotherapy before total mesorectal excision (TME) versus preoperative chemoradiotherapy, TME, and optional adjuvant chemotherapy in locally advanced rectal cancer (RAPIDO): a randomised, open-label, phase 3 trial.

Lancet Oncol. 2021-1

[7]
Is adjuvant chemotherapy necessary for patients with pathological complete response after neoadjuvant chemoradiotherapy and radical surgery in locally advanced rectal cancer? Long-term analysis of 40 ypCR patients at a single center.

Int J Colorectal Dis. 2016-6

[8]
Selective lateral lymph node dissection after neoadjuvant chemoradiotherapy in rectal cancer.

World J Gastroenterol. 2020-6-7

[9]
Recurrence rates and prognostic factors in ypN0 rectal cancer after neoadjuvant chemoradiation and total mesorectal excision.

Ann Surg Oncol. 2011-5-18

[10]
Neoadjuvant chemotherapy with modified FOLFOXIRI for locally advanced rectal cancer to transform effectively EMVI and MRF from positive to negative: results of a long-term single center phase 2 clinical trial.

BMC Cancer. 2023-6-27

引用本文的文献

[1]
Development of a cancer-specific survival assessment for lymph node-positive colorectal cancer patients treated with adjuvant chemotherapy.

Front Surg. 2025-5-12

[2]
The role of adjuvant chemotherapy in rectal cancer: A nationwide cohort study from the Netherlands.

Colorectal Dis. 2025-3

[3]
[AKBA combined with doxorubicin inhibits proliferation and metastasis of triple-negative breast cancer MDA-MB-231 cells and xenograft growth in nude mice].

Nan Fang Yi Ke Da Xue Xue Bao. 2024-12-20

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索