Evidence map›Paper›PMID 19813061›Full record

ArticleAnnals of surgical oncology2010

KRAS mutation and microsatellite instability: two genetic markers of early tumor development that influence the prognosis of colorectal cancer.

Garrett M Nash, Mark Gimbel, Alfred M Cohen, Zhao-Shi Zeng, Mackevin I Ndubuisi, Daniel R Nathanson, Jurg Ott, Francis Barany, Philip B Paty

Open access · greenAbstract read
In one paragraph

Article in Annals of surgical oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 4 pooled it
4.7field-weighted citation impact, top 5% 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

52 citing papers in PubMed, 4 syntheses or guidelines pooled it, 92 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Garrett M NashDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, USA.
Mark Gimbel
Alfred M Cohen
Zhao-Shi Zeng
Mackevin I Ndubuisi
Daniel R Nathanson
Jurg Ott
Francis Barany
Philip B Paty
Memorial Sloan Kettering Cancer Center · USCornell University · USRockefeller University · USUniversity of Arizona Cancer Center

Funding

NEW METHODS FOR CANCER DETECTIONP01CA065930 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BARANY, FRANCIS · 1997 to 2007
$14.1M
NCI NIH HHS 2 P01 CA65930-05A2NCI NIH HHS P01 CA065930
6 · The paper itself

Abstract

introductionWe examined two genetic markers established early in colorectal tumor development, microsatellite instability (MSI) and mutation of the KRAS proto-oncogene, to see if these genetic changes influence metastatic disease progression and survival. PATIENTS AND

methodsMSI and KRAS mutation status were assessed in 532 primary adenocarcinomas (stage I-IV) from patients treated by colon resection. Median follow-up was 4.1 years (range 0-13.3 years) overall, 5.4 years for survivors.

resultsMSI and KRAS mutation were detected in 12 and 36% of cases, respectively. MSI was more common in early-stage disease (I, 15%; II, 21%; III, 10%; IV, 2%; P = 0.0001). Prevalence of KRAS mutation did not vary with stage (I, 36%; II, 34%; III, 35%; IV, 40%; P = ns). Disease-specific survival was far superior for MSI tumors than for microsatellite stability (MSS) tumors (5-year survival 92 vs. 59%, P < 0.0001). KRAS mutation was a marker of poor survival (5-year survival 55 vs. 68%, P = 0.0002). Using Cox regression analysis MSI, KRAS mutation, and stage were strong independent predictors of survival in the entire patient population. A high-mortality group with MSS/KRAS-mutant tumors was identified within the stage I and II cohort.

conclusionsMSI and KRAS mutation provide fundamental genetic signatures influencing tumor behavior across patient subsets and stages of tumor development.

Indexed as

Microsatellite InstabilityAdenocarcinomaAdultAgedAged, 80 and overColonColorectal NeoplasmsDisease ProgressionFemaleFollow-Up StudiesGenetic MarkersHumansMaleMiddle AgedMutationProto-Oncogene MasGenetic MarkersKRAS protein, humanMAS1 protein, humanProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)ras Proteins

Identifiers

PMID19813061
PMCPMC4380015
OpenAlexW1999946645

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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.