Evidence map›Paper›PMID 19934290›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2009

KRAS mutation in stage III colon cancer and clinical outcome following intergroup trial CALGB 89803.

Shuji Ogino, Jeffrey A Meyerhardt, Natsumi Irahara, Donna Niedzwiecki, Donna Hollis, Leonard B Saltz, Robert J Mayer, Paul Schaefer, Renaud Whittom, Alexander Hantel and 8 more

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 1% 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

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 196 citations in OpenAlex.

  1. Pooled it
  2. Evaluating the utility ofEpigenetics · 2024
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  13. Predictive and prognostic roles of BRAF mutation in stage III colon cancer: results from intergroup trial CALGB 89803.Clinical cancer research : an official journal of the American Association for Cancer Research · 2012
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  15. Cetuximab for the treatment of advanced bronchioloalveolar carcinoma (BAC): an Eastern Cooperative Oncology Group phase II study (ECOG 1504).Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Trial
  16. Article
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  19. Reclassification ofTherapeutic advances in medical oncology · 2024
    Article
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49 more citing papers are in PubMed but not listed here.

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

18 authors at 8 institutions in 1 country.

Shuji OginoDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts 02115, USA. shuji_ogino@dfci.harvard.edu
Jeffrey A Meyerhardt
Natsumi Irahara
Donna Niedzwiecki
Donna Hollis
Leonard B Saltz
Robert J Mayer
Paul Schaefer
Renaud Whittom
Alexander Hantel
Al B Benson
Richard M Goldberg
Monica M Bertagnolli
Charles S Fuchs
Cancer and Leukemia Group B
North Central Cancer Treatment Group
Canadian Cancer Society Research Institute
Southwest Oncology Group
Community Hospital · USDuke Medical Center · USLoyola University Chicago · USMemorial Sloan Kettering Cancer Center · USNorthwestern University · USUniversity of North Carolina at Chapel Hill · USBrigham and Women's Hospital · USDuke University Hospital · US

Funding

CANCER AND LEUKEMIA GROUP B MINORITY SATELLITE SUPPLEMENU10CA031946 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 1985 to 2013
$158.4M
SOUTHWEST ONCOLOGY GROUP--STATISTICAL CENTERU10CA038926 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEBLANC, MICHAEL L. · 1985 to 2013
$69.8M
CANCER &LEUKEMIA GROUP B STATISTICAL CENTERU10CA033601 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SARGENT, DANIEL J. · 1985 to 2013
$69.4M
PROVIDE STATISTICAL SERVICESU10CA023318 · NCI · DANA-FARBER CANCER INSTITUTE · PI GRAY, ROBERT J · 1985 to 2013
$33.4M
Tissue and Pathology ResourcesP50CA127003 · NCI · DANA-FARBER CANCER INST · PI EL-BARDEESY, NABEEL, SELLERS, WILLIAM R · 2007 to 2023
$33.2M
SOUTHEAST CANCER CONTROL COSORTIUM, INCU10CA045808 · NCI · SOUTHEAST CLINICAL ONCOL RES CONSORTIUM · PI ATKINS, JAMES NORMAN · 1987 to 2013
$26.6M
MULTIDISCIPLINARY CLINICAL AND TRANSLATIONAL SCIENCE (MCTS) PROGRAM (UL1)UL1RR025741 · NCRR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GREENLAND, PHILIP · 2008 to 2011
$24.7M
MEDICAL CENTER OF DELAWARE CCOPU10CA045418 · NCI · CHRISTIANA CARE HEALTH SERVICES, INC. · PI GRUBBS, STEPHEN S. · 1987 to 2014
$14.5M
TOLEDO COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA035415 · NCI · TOLEDO COMMUNITY HOSPITAL ONCOLOGY PROG · PI MOWAT, REX BRADLEY · 1985 to 2014
$9.9M
SOUTHERN NEVADA CANCER RESEARCH FOUNDATION-CCOPU10CA035421 · NCI · SOUTHERN NEVADA CANCER RESEARCH FDN · PI ELLERTON, JOHN A · 1985 to 2014
$9.8M
MOUNT SINAI COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA045564 · NCI · MOUNT SINAI MEDICAL CENTER (MIAMI BEACH) · PI SCHWARTZ, MICHAEL ALAN · 1987 to 2014
$9.2M
UNIVERSITY OF ILLINOIS MINORITY BASED CCOPU10CA074811 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PEACE, DAVID J · 1997 to 2011
$8.5M
NCI NIH HHS CA31946NCI NIH HHS CA33601NCI NIH HHS K07 CA122826NCI NIH HHS P50 CA127003NCI NIH HHS R01 CA118553NCI NIH HHS U10 CA003927NCI NIH HHS U10 CA007968NCI NIH HHS U10 CA021060NCI NIH HHS U10 CA023318NCI NIH HHS U10 CA031946NCI NIH HHS U10 CA032291NCI NIH HHS U10 CA033601NCI NIH HHS U10 CA035279NCI NIH HHS U10 CA035415NCI NIH HHS U10 CA035421NCI NIH HHS U10 CA038926NCI NIH HHS U10 CA041287NCI NIH HHS U10 CA045389NCI NIH HHS U10 CA045418NCI NIH HHS U10 CA045564NCI NIH HHS U10 CA045808NCI NIH HHS U10 CA046282NCI NIH HHS U10 CA047559NCI NIH HHS U10 CA047577NCI NIH HHS U10 CA047642NCI NIH HHS U10 CA071323NCI NIH HHS U10 CA074811NCI NIH HHS U10 CA077440NCI NIH HHS U10 CA077597NCI NIH HHS U10 CA077651NCI NIH HHS U10 CA077658NCI NIH HHS U10 CA114558NCI NIH HHS U10 CA180850NCRR NIH HHS UL1 RR025741
6 · The paper itself

Abstract

purposeAlterations in the RAS and RAF pathway relate to epigenetic and epigenomic aberrations, and are important in colorectal carcinogenesis. KRAS mutation in metastatic colorectal cancer predicts resistance to anti-epidermal growth factor receptor (EGFR)-targeted therapy (cetuximab or panitumumab). It remains uncertain, however, whether KRAS mutation predicts prognosis or clinical outcome of colon cancer patients independent of anti-EGFR therapy.

methodsWe conducted a study of 508 cases identified among 1,264 patients with stage III colon cancer who enrolled in a randomized adjuvant chemotherapy trial (5-fluorouracil, leucovorin with or without irinotecan) in 1999-2001 (CALGB 89803). KRAS mutations were detected in 178 tumors (35%) by pyrosequencing. Kaplan-Meier and Cox proportional hazard models assessed the prognostic significance of KRAS mutation and adjusted for potential confounders including age, sex, tumor location, tumor/node stage, performance status, adjuvant chemotherapy arm, and microsatellite instability status.

resultsCompared with patients with KRAS-wild-type tumors, patients with KRAS-mutated tumors did not experience any difference in disease-free, recurrence-free, or overall survival. The 5-year disease-free, recurrence-free, and overall survival rates (KRAS-mutated versus KRAS-wild-type patients) were 62% versus 63% (log-rank P = 0.89), 64% versus 66% (P = 0.84), and 75% versus 73% (P = 0.56), respectively. The effect of KRAS mutation on patient survival did not significantly differ according to clinical features, chemotherapy arm, or microsatellite instability status, and the effect of adjuvant chemotherapy assignment on outcome did not differ according to KRAS status.

conclusionsIn this large trial of chemotherapy in stage III colon cancer patients, KRAS mutational status was not associated with any significant influence on disease-free or overall survival.

Indexed as

Genes, rasMutationAdultAgedAntineoplastic AgentsCamptothecinColonic NeoplasmsDisease-Free SurvivalFemaleHumansIrinotecanMaleMicrosatellite RepeatsMiddle AgedOncogene Protein p21(ras)Proportional Hazards ModelsAntineoplastic AgentsCamptothecinIrinotecanOncogene Protein p21(ras)

Identifiers

PMID19934290
PMCPMC2787689
OpenAlexW2104573387

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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.