Evidence map›Paper›PMID 32394229›Full record

ArticleCancer causes & control : CCC2020

Association of KRAS mutation with tumor deposit status and overall survival of colorectal cancer.

Meifang Zhang, Wenwei Hu, Kun Hu, Yong Lin, Zhaohui Feng, Jing-Ping Yun, Nan Gao, Lanjing Zhang

Open access · greenAbstract read
In one paragraph

Article in Cancer causes & control : CCC, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Tumor Deposit Is an Independent Factor Predicting Early Recurrence and Poor Prognosis in Gastric Cancer.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
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 3 countries.

Meifang ZhangDepartment of Pathology, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Wenwei HuRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Kun HuDepartment of Pathology, University at Buffalo, Buffalo, NY, USA.
Yong LinRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Zhaohui FengRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Jing-Ping YunDepartment of Pathology, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Nan GaoDepartment of Biological Sciences, Rutgers University, Newark, NJ, USA.
Lanjing ZhangRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA. lanjing.zhang@rutgers.edu.ORCID http://orcid.org/0000-0001-5436-887X
Rutgers, The State University of New Jersey · USSun Yat-sen University · CNUniversity at Buffalo, State University of New York · US

Funding

Mucosal modulation by LGG and R. gnavus specific tryptophan metabolitesR01AT010243 · NCCIH · RUTGERS THE STATE UNIV OF NJ NEWARK · PI FERRARIS, RONALDO PARAOAN, GAO, NAN · 2018 to 2021
$1.6M
National Natural Science Foundation of China 81872387NCCIH NIH HHS R01 AT010243NIH HHS AT010243
6 · The paper itself

Abstract

purposeTo examine associations of KRAS mutation with tumor deposit status and overall survival in colorectal cancer (CRC) patients.

methodsThis retrospective cohort study included patients with incidental CRC diagnosed during 2010-2014 and recorded statuses of KRAS and tumor deposit in the National Cancer Database of the USA. Multivariable logistic regression and time-varying Cox regression analyses were used.

resultsWe included 45,761 CRC patients with KRAS status (24,027 [52.5%] men, 24,240 [53.0%] < 65 years old, 17,338 [37.9%] with KRAS mutation). Adjusted for microsatellite instability, age, pathologic stage and tumor grade, KRAS mutation (versus wild type) was associated with tumor deposit presence (odds ratio = 1.11, 95% CI 1.02-1.20). KRAS mutation was also linked to worse overall survival of CRC patients regardless of tumor deposit status (adjusted Hazard ratio [HR] = 1.20, 95% CI 1.07-1.33 for CRC with tumor deposits, and adjusted HR = 1.24, 95% CI 1.14-1.35 or CRC without) or tumor stage (adjusted HR = 1.32, 95% CI 1.14-1.54 for early-stage and adjusted HR = 1.18, 95% CI 1.10-1.27 for late-stage). Microsatellite instability was associated with better overall survival in CRC without tumor deposit (adjusted HR = 0.89, 95% CI 0.79-0.99), but not in CRC with tumor deposit (adjusted HR = 1.12, 95% CI 0.97-1.30).

conclusionKRAS mutation is independently associated with tumor deposit presence and a worse overall survival in CRC patients.

Indexed as

MutationAgedCohort StudiesColorectal NeoplasmsFemaleHumansLogistic ModelsMaleMicrosatellite InstabilityMiddle AgedPrognosisProportional Hazards ModelsProto-Oncogene Proteins p21(ras)Retrospective StudiesUnited StatesKRAS protein, humanProto-Oncogene Proteins p21(ras)BiomarkerColorectal cancerKRASMicrosatellite instabilitySurvival rate

Identifiers

PMID32394229
PMCPMC7319095
OpenAlexW3025097160

What OpenQuestion holds

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Registered trials

None linked

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.