Evidence map›Paper›PMID 35484252›Full record

ArticleInternational journal of colorectal disease2022

The prognostic value of KRAS mutation in locally advanced rectal cancer.

Palash Asawa, Veli Bakalov, Pragnan Kancharla, Stephen Abel, Zena Chahine, Dulabh K Monga, Alexander V Kirichenko, Rodney E Wegner

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Article in International journal of colorectal disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 17% of its field
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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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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

8 authors at 3 institutions in 1 country.

Palash AsawaDepartment of Internal Medicine, Allegheny Health Network, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
Veli BakalovDivision of Medical Oncology, Allegheny Health Network Cancer Institute, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
Pragnan KancharlaDivision of Medical Oncology, Allegheny Health Network Cancer Institute, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
Stephen AbelDivision of Radiation Oncology, Allegheny General Hospital, Allegheny Health Network Cancer Institute, Level 02, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
Zena ChahineMarkey Cancer Center, University of Kentucky, 800 Rose St, Lexington, KY, 40536, USA.
Dulabh K MongaDivision of Medical Oncology, Allegheny Health Network Cancer Institute, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
Alexander V KirichenkoDivision of Radiation Oncology, Allegheny General Hospital, Allegheny Health Network Cancer Institute, Level 02, 320 E. North Avenue, Pittsburgh, PA, 15212, USA.
Rodney E WegnerDivision of Radiation Oncology, Allegheny General Hospital, Allegheny Health Network Cancer Institute, Level 02, 320 E. North Avenue, Pittsburgh, PA, 15212, USA. Rodney.wegner@ahn.org.
Allegheny Health Network · USAllegheny General Hospital · USMarkey Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognostic value of the KRAS proto-oncogene mutation in colorectal cancer has been debated. Herein, we analyzed the National Cancer Database (NCDB) to assess the role of KRAS mutation as a prognostic marker in patients with locally advanced rectal cancer (LARC).

methodsWe identified LARC patients treated with neoadjuvant chemoradiation from 2004-2015 excluding those with stage I/IV disease and unknown KRAS status. Multivariable logistic regression identified variables associated with KRAS positivity. Propensity adjusted univariable and multivariable analyses identified predictors of survival.

resultsOf the 784 eligible patients, 506 were KRAS-negative (KRAS -) and 278 were KRAS-positive (KRAS +). Median survival was 63.6 months and 76.3 months for KRAS + and KRAS - patients respectively, with propensity adjusted 3 and 5-year survival of 79.9% vs. 83.6% and 56.7% vs. 61.9% respectively (HR 1.56, p 1.074-2.272). Male sex, no insurance, and KRAS + disease were associated with poorer survival on unadjusted and propensity adjusted multivariable analyses.

conclusionsOur analysis of KRAS + LARC suggest that KRAS + disease is associated with poorer overall survival. Given the inherent limitations of retrospective data, prospective validation is warranted.

Indexed as

Proto-Oncogene Proteins p21(ras)Rectal NeoplasmsHumansMaleMutationPrognosisRetrospective StudiesKRAS protein, humanProto-Oncogene Proteins p21(ras)Colorectal cancersGene mutationsKRAS mutationLocally advanced rectal cancerPrognostic value

Identifiers

PMID35484252
OpenAlexW4226051820

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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.