Evidence map›Paper›PMID 39871125›Full record

ArticleBMC gastroenterology2025

Effect of KRAS mutation status on clinicopathological characteristics and overall survival in patients with rectal cancer.

Shengbin Zheng, Zhijie You, Guodon Guo, Zhijing Lin, Siming Wang, Guohua Yang

Abstract read
In one paragraph

Article in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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.

Shengbin ZhengDepartment of Gastrointestinal Surgery, Fujian Medical University Provincial Clinical College FuZhou FuJiang, Fuzhou, China.
Zhijie YouDepartment of Internal Medicine, Fujian Medical University Provincial Clinical College FuZhou FuJiang, Fuzhou, China.
Guodon GuoDepartment of Internal Medicine, Fujian Medical University Provincial Clinical College FuZhou FuJiang, Fuzhou, China.
Zhijing LinDepartment of Gastrointestinal Surgery, Fujian Medical University Provincial Clinical College FuZhou FuJiang, Fuzhou, China.
Siming WangDepartment of Gastrointestinal Surgery, Fujian Medical University Provincial Clinical College FuZhou FuJiang, Fuzhou, China.
Guohua YangDepartment of Gastrointestinal Surgery, Fujian Medical University Provincial Clinical College FuZhou FuJiang, Fuzhou, China. 344050633@qq.com.

Funding

Fujian Provincial Health Commission Middle-Young-Generation Talent Cultivation Project 2020GGB007
6 · The paper itself

Abstract

backgroundKRAS mutations in rectal cancer are associated with a conflict prognosis. This study aimed to compare clinicopathological outcomes of patients and tumor criteria between wKRAS and mKRAS, as well as overall survival in the two groups.

methodsThe research retrospectively analyzed a cohort of 193 patients who received surgical treatment for rectal adenocarcinoma between May 2015 and December 2023. The patients were categorized into two groups according to their KRAS status: wild-type KRAS (wKRAS) and mutant KRAS (mKRAS), with performing research on mKRAS

resultsThe mKRAS group included 100 patients(51.8%) and had no significantly difference in age, sex, distance from anus, tumor node metastasis(TNM), lymphovascular invasion(LVI), grade differentiation, and perineural invasion(PNI), carcinoembryonic antigen(CEA) level than that in wKRAS group.KRAS

conclusionThe overall survival duration for wKRAS was superior to that of mKRAS; however, the difference between the two groups was not statistically significant. In contrast, the survival time for KRAS RETROSPECTIVELY REGISTERED: K2024-07-037.2024,7.

Indexed as

AdenocarcinomaProto-Oncogene Proteins p21(ras)Rectal NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedMutationNeoplasm InvasivenessNeoplasm StagingPrognosisRetrospective StudiesKRAS protein, humanProto-Oncogene Proteins p21(ras)KRAS mutationOverall survival Clinicopathological outcomesPrognosisRectal cancer

Identifiers

PMID39871125
PMCPMC11770934

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Registered trials

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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.