Evidence map›Paper›PMID 40386595›Full record

ArticleJournal of gastrointestinal oncology2025

Prognostic nomogram for T3-T4 primary colorectal cancer patients with perineural invasion after surgery: a Surveillance, Epidemiology, and End Results program database analysis.

Hui Wu, Xue Liu, Haitao Chen, Qinghua Yao

Abstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hui Wu *The Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China.
Xue Liu *Postgraduate Training Base Alliance of Wenzhou Medical University (Zhejiang Cancer Hospital), Hangzhou, China.
Haitao ChenDepartment of Medical Oncology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Qinghua YaoDepartment of Medical Oncology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) is a common malignancy, with T3-T4 primary CRC characterized by perineural invasion (PNI), representing an aggressive subtype with poor prognosis. This study aimed to develop and validate prognostic nomograms for predicting overall survival (OS) and cancer-specific survival (CSS) in patients with T3-T4 primary CRC and PNI after surgery. Methods: Data were extracted from the Surveillance, Epidemiology, and End Results (SEER) database, focusing on patients diagnosed with T3-T4 primary CRC and PNI between 2000 and 2019. Eligible patients were randomly divided into training and validation cohorts. Univariate and multivariate Cox regression analyses were conducted to identify independent prognostic factors, which were integrated into nomograms for OS and CSS. The nomograms were assessed using the concordance index (C-index), receiver operating characteristic (ROC) curves, calibration plots, and decision curve analysis (DCA). Results: A total of 7,808 patients met the inclusion criteria. Significant prognostic factors identified in the multivariate analysis included age, sex, race, marital status, site, Tumor (T) stage of the Tumor, Node, Metastasis (TNM) staging system, radiation, regional node positive, liver and lung metastasis, tumor size, histologic type, median household income, and SEER summary stage. The nomograms exhibited good predictive accuracy, with C-indexes of 0.7422 for OS in the training cohort and 0.7428 in the validation cohort. The nomograms were validated using ROC curves, calibration plots, and DCA, which confirmed the models' reliability and clinical utility. Conclusions: The developed nomograms are robust tools for predicting 3-, 5-, and 10-year OS and CSS in patients with T3-T4 primary CRC and PNI after surgery. These tools help clinicians create personalized treatment plans and improve patient outcomes.

Indexed as

cancer-specific survival (CSS)Colorectal cancer (CRC)overall survival (OS)perineural invasion (PNI)Surveillance, Epidemiology, and End Results (SEER)

Identifiers

PMID40386595
PMCPMC12078831

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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.