Evidence map›Paper›PMID 41417446›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Clinical and prognostic implications of RAS mutations in metastatic colorectal cancer.

Evrim Ataca, Merve Keskinkilic, Sulen Sarioglu, Yasemin Basbinar, Tugba Yavuzsen

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Evrim AtacaDepartment of Internal Medicine, Faculty of Medicine, Dokuz Eylul University, Izmir, Türkiye. evrimbayrakdar@gmail.com.ORCID http://orcid.org/0000-0001-6572-0277
Merve KeskinkilicDepartment of Medical Oncology, Izmir Democracy University Buca Seyfi Demirsoy Training and Research Hospital, Izmir, Türkiye.
Sulen SariogluDepartment of Pathology, Faculty of Medicine, Dokuz Eylul University, Izmir, Türkiye.
Yasemin BasbinarDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylul University, Izmir, Türkiye.
Tugba YavuzsenDivision of Medical Oncology, Department of Internal Medicine, Faculty of Medicine, Dokuz Eylul University, Izmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRAS mutations play a critical role in the pathogenesis and progression of colorectal cancer. This study aimed to evaluate the clinical and pathological characteristics associated with RAS mutation status and to investigate its prognostic value in patients with metastatic colorectal cancer.

methodsThis retrospective study included 446 adult patients with metastatic colorectal cancer followed at Dokuz Eylul University Medical Oncology Department between 2010 and 2016, all of whom had available RAS mutation data and complete clinical records.

resultsRAS mutations were identified in 44.8% of patients, predominantly KRAS codon 12 mutations. Early-stage disease and absence of metastasis at diagnosis were more common in the RAS wild-type (WT) group (p < 0.001). Lung metastases occurred more frequently in RAS-mutant cases (p = 0.006). No significant difference in overall survival (OS) was observed between RAS-mutant and WT groups (53.6 vs. 52.5 months; p > 0.05). Anti-VEGF therapy conferred a modest OS benefit in RAS-mutant patients, whereas anti-EGFR therapy showed no effect. Among KRAS-mutant subtypes, codon 61 mutations were associated with the poorest OS.

conclusionRAS mutation status may provide insight into metastatic patterns and disease stage in patients with metastatic colorectal cancer. However, its impact on overall survival remains inconclusive. Further prospective studies are needed to clarify its prognostic value.

Indexed as

Colorectal NeoplasmsMutationProto-Oncogene Proteins p21(ras)AdultAgedAged, 80 and overErbB ReceptorsFemaleHumansLung NeoplasmsMaleMiddle AgedPrognosisRetrospective StudiesSurvival RateErbB ReceptorsKRAS protein, humanProto-Oncogene Proteins p21(ras)Colorectal cancerKRASMetastasisNRASOverall survivalPrognostic factorsRAS mutation

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.