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结直肠癌最早期阶段淋巴结获取量的预后价值:一项多中心队列研究

The prognostic value of lymph node yield in the earliest stage of colorectal cancer: a multicenter cohort study.

作者信息

Backes Yara, Elias Sjoerd G, Bhoelan Bibie S, Groen John N, van Bergeijk Jeroen, Seerden Tom C J, Pullens Hendrikus J M, Spanier Bernhard W M, Geesing Joost M J, Kessels Koen, Kerkhof Marjon, Siersema Peter D, de Vos Tot Nederveen Cappel Wouter H, van Lelyveld Niels, Wolfhagen Frank H J, Ter Borg Frank, Offerhaus G Johan A, Lacle Miangela M, Moons Leon M G

机构信息

Department of Gastroenterology & Hepatology, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA, Utrecht, The Netherlands.

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

BMC Med. 2017 Jul 14;15(1):129. doi: 10.1186/s12916-017-0892-7.

Abstract

BACKGROUND

In patients with stage II colorectal cancer (CRC) the number of surgically retrieved lymph nodes (LNs) is associated with prognosis, resulting in a minimum of 10-12 retrieved LNs being recommended for this stage. Current guidelines do not provide a recommendation regarding LN yield in T1 CRC. Studies evaluating LN yield in T1 CRC suggest that such high LN yields are not feasible in this early stage, and a lower LN yield might be appropriate. We aimed to validate the cut-off of 10 retrieved LNs on risk for recurrent cancer and detection of LN metastasis (LNM) in T1 CRC, and explored whether this number is feasible in clinical practice.

METHODS

Patients diagnosed with T1 CRC and treated with surgical resection between 2000 and 2014 in thirteen participating hospitals were selected from the Netherlands Cancer Registry. Medical records were reviewed to collect additional information. The association between LN yield and recurrence and LNM respectively were analyzed using 10 LNs as cut-off. Propensity score analysis using inverse probability weighting (IPW) was performed to adjust for clinical and histological confounding factors (i.e., age, sex, tumor location, size and morphology, presence of LNM, lymphovascular invasion, depth of submucosal invasion, and grade of differentiation).

RESULTS

In total, 1017 patients with a median follow-up time of 49.0 months (IQR 19.6-81.5) were included. Four-hundred five patients (39.8%) had a LN yield ≥ 10. Forty-one patients (4.0%) developed recurrence. LN yield ≥ 10 was independently associated with a decreased risk for recurrence (IPW-adjusted HR 0.20; 95% CI 0.06-0.67; P = 0.009). LNM were detected in 84 patients (8.3%). LN yield ≥ 10 was independently associated with increased detection of LNM (IPW-adjusted OR 2.27; 95% CI 1.39-3.69; P = 0.001).

CONCLUSIONS

In this retrospective observational study, retrieving < 10 LNs was associated with an increased risk of CRC recurrence, advocating the importance to perform an appropriate oncologic resection of the draining LNs and diligent LN search when patients with T1 CRC at high-risk for LNM are referred for surgical resection. Given that both gastroenterologists, surgeons and pathologists will encounter T1 CRCs with increasing frequency due to the introduction of national screening programs, awareness on the consequences of an inadequate LN retrieval is of utmost importance.

摘要

背景

在II期结直肠癌(CRC)患者中,手术切除的淋巴结(LN)数量与预后相关,因此建议该阶段至少获取10 - 12个淋巴结。目前的指南未就T1期CRC的淋巴结获取量提供建议。评估T1期CRC淋巴结获取量的研究表明,在这个早期阶段获得如此高的淋巴结获取量是不可行的,较低的淋巴结获取量可能更为合适。我们旨在验证T1期CRC中获取10个淋巴结对癌症复发风险和淋巴结转移(LNM)检测的临界值,并探讨这个数量在临床实践中是否可行。

方法

从荷兰癌症登记处选取2000年至2014年期间在13家参与医院被诊断为T1期CRC并接受手术切除的患者。查阅病历以收集额外信息。以10个淋巴结为临界值,分别分析淋巴结获取量与复发和LNM之间的关联。采用逆概率加权(IPW)进行倾向评分分析,以调整临床和组织学混杂因素(即年龄、性别、肿瘤位置、大小和形态、LNM的存在、淋巴管侵犯、黏膜下侵犯深度和分化程度)。

结果

共纳入1017例患者,中位随访时间为49.0个月(IQR 19.6 - 81.5)。405例患者(39.8%)的淋巴结获取量≥10个。41例患者(4.0%)出现复发。淋巴结获取量≥10个与复发风险降低独立相关(IPW调整后的HR 0.20;95% CI 0.06 - 0.67;P = 0.009)。84例患者(8.3%)检测到LNM。淋巴结获取量≥10个与LNM检测增加独立相关(IPW调整后的OR 2.27;95% CI 1.39 - 3.69;P = 0.001)。

结论

在这项回顾性观察研究中,获取的淋巴结<10个与CRC复发风险增加相关,这表明当LNM高危的T1期CRC患者被转诊进行手术切除时,进行适当的肿瘤引流淋巴结切除和仔细的淋巴结搜索非常重要。鉴于由于国家筛查计划的引入,胃肠病学家、外科医生和病理学家将越来越频繁地遇到T1期CRC,认识到淋巴结获取不足的后果至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19ee/5512847/2fce2e4d3dea/12916_2017_892_Fig1_HTML.jpg

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