Evidence map›Paper›PMID 40640480›Full record

ArticleAnnals of surgical oncology2025

Discrepancies in the Reactivity of Mesorectal versus Lateral Lymph Nodes Post-Neoadjuvant Chemoradiotherapy for Rectal Cancer: Insights from Radiological and Pathological Perspectives.

Zixuan Zhuang, Xuyang Yang, Yang Zhang, Xiangbing Deng, Mingtian Wei, Ziqiang Wang

Abstract readComparative Study
In one paragraph

Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Zixuan ZhuangColorectal Cancer Center, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
Xuyang YangColorectal Cancer Center, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
Yang ZhangColorectal Cancer Center, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
Xiangbing DengColorectal Cancer Center, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
Mingtian WeiColorectal Cancer Center, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China. 826627010@qq.com.
Ziqiang WangColorectal Cancer Center, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China. wangziqiang@scu.edu.cn.

Funding

1·3·5 project for disciplines of excellence, West China Hospital, Sichuan University 2019HXFH0311·3·5 project for disciplines of excellence, West China Hospital, Sichuan University 20HXJS003Ethicon Excellent in Surgery Grant (EESG) HZB-20190528-4Post-Doctor Research Project, West China Hospital, Sichuan University 2021HXBH033Science and Technology Department of Sichuan Province 2021YFS0025
6 · The paper itself

Abstract

introductionThe heterogeneous treatment response of lateral lymph nodes (LLN) and mesorectal lymph nodes (MLN) to neoadjuvant chemoradiotherapy (NCRT) in locally advanced rectal cancer (LARC) remains poorly understood. This study investigates imaging regression patterns, pathological lymph node regression grade (LRG), and prognostic implications in patients with LARC undergoing radical resection and lateral lymph node dissection (LLND) after NCRT. PATIENTS AND

methodsA total of 110 patients with LARC undergoing radical resection and LLND after NCRT (2018-2024) were enrolled. Visible MLNs and LLNs on initial magnetic resonance imaging (MRI) were matched node-by-node on post-NCRT MRI, and short-axis (SA) diameter regression was calculated. Pathological LRG scores, including LRG-max, LRG-sum, and LRG-ratio, were assessed on the basis of tumor cell proportion and fibrosis. Differences in radiological and pathological regression between MLNs and LLNs were analyzed at lymph node (LN) and patient levels.

resultsMRI assessed 1744 LNs (811 MLNs, 933 LLNs pre-NCRT; 546 MLNs, 969 LLNs post-NCRT). MLNs exhibited higher disappearance rates (32.7% versus 2.4%, P < 0.0001) and greater SA regression (0.596 ± 0.333 versus 0.214 ± 0.242, P < 0.0001) than LLNs. Histopathological re-evaluation of 2108 LNs (916 MLNs, 1192 LLNs) revealed LLNs had higher LRG-max (37.13 versus 21.37, P = 0.011) and LRG-ratio (3.45 ± 1.29 versus 2.47 ± 0.96, P = 0.0003). LRG-sum was an independent prognostic factor for both MLNs and LLNs.

conclusionsLLNs demonstrated lower imaging regression, higher pathological residual cancer, and poorer treatment response compared with MLNs, indicating greater NCRT tolerance.

Indexed as

Chemoradiotherapy, AdjuvantLymph NodesNeoadjuvant TherapyRectal NeoplasmsAdultAgedFemaleFollow-Up StudiesHumansLymphatic MetastasisLymph Node ExcisionMagnetic Resonance ImagingMaleMiddle AgedPrognosisRetrospective StudiesLateral lymph nodesLymph node regression gradeMesorectal lymph nodesNeoadjuvant chemoradiotherapyPrognosisRectal cancer

Identifiers

PMID40640480
PMCPMC12454576

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.