Evidence map›Paper›PMID 37608030›Full record

ArticleJournal of gastrointestinal cancer2024

Overall Survival, BRAF, RAS, and MSI Status in Patients Who Underwent Cetuximab After Refractory Chemotherapy for Metastatic Colorectal Cancer.

Florinda A Santos, Rui Manuel Reis, Lucas C Barroti, Allan A L Pereira, Marcus M Matsushita, Ana Carolina de Carvalho, José Guilherme Datorre, Gustavo N Berardinelli, Raphael L C Araujo

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Article in Journal of gastrointestinal cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 32% 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

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

  1. Pooled it
  2. Article
  3. 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

9 authors at 3 institutions in 2 countries.

Florinda A SantosDepartment of Oncology, Barretos Cancer Hospital, Barretos, Brazil.
Rui Manuel ReisMolecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
Lucas C BarrotiDepartment of Dermatology, Universidade Federal de Sao Paulo, Sao Paulo, Brazil.
Allan A L PereiraClinical Oncology Department, Hospital Sirio Libanes de Brasilia-DF, Sao Paulo, Brazil.
Marcus M MatsushitaDepartment of Pathology, Barretos Cancer Hospital, Barretos, Brazil.
Ana Carolina de CarvalhoDepartment of Pathology, Barretos Cancer Hospital, Barretos, Brazil.
José Guilherme DatorreMolecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
Gustavo N BerardinelliLaboratory of Molecular Diagnostic, Barretos Cancer Hospital, Barretos, Brazil.
Raphael L C AraujoDepartment of Surgery, Digestive Surgery Service, Universidade Federal de Sao Paulo, Sao Paulo, Brazil. raphael.l.c.araujo@gmail.com.ORCID http://orcid.org/0000-0002-7834-5944
Hospital de Câncer de Barretos · BRHospital Sírio-Libanês · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEvaluate overall survival (OS), RAS, BRAF, and MSI frequencies in patients with metastatic colorectal cancer (mCRC), refractory to chemotherapy, and finally treated with cetuximab.

methodsA retrospective cohort study to evaluate 211 mCRC patients with wild-type KRAS treated with cetuximab. BRAF V600E, KRAS, NRAS gene mutations, and MSI status were identified using PCR techniques in a population of pre-treated patients who were refractory to fluoropyrimidines, oxaliplatin, and irinotecan. In addition, we evaluated the mutation frequency of the BRAF and NRAS genes and the MSI status of this population. Uni- and multivariate analyses were performed for independent prognostic factors of OS.

resultsThe median OS was 10.4 months, 6.6 months for patients with right and 11.5 months for left colon cancers (p = 0.02). The frequencies of mutations were BRAF at 3.9% (median OS of 4.9 months), NRAS at 3.38% (median OS of 6.9 months), and MSI-High status at 3.3% (median OS of 4.6 months). The OS, NRAS, and MSI frequencies were similar to those found in other studies that evaluated cetuximab in poly-treated patients and were associated with lower survival rates in univariate analyses. The frequency of BRAF mutations was lower than that found in previous studies. The only variable that remained significant for OS in the multivariate model was tumour laterality, with patients with right colon cancer presenting a worse prognosis (HR = 2.81).

conclusionAlthough BRAF, NRAS mutations, and MSI-High status were associated with shorter OS in univariate analyses, only tumour laterality remained an independent prognostic factor in the multivariate analysis.

Indexed as

CetuximabColorectal NeoplasmsGTP PhosphohydrolasesProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)AdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsDrug Resistance, NeoplasmFemaleHumansMaleMembrane ProteinsMicrosatellite InstabilityAntineoplastic Agents, ImmunologicalCetuximabGTP PhosphohydrolasesMembrane ProteinsProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)BRAFCetuximabChemotherapyEpidermal growth factor receptorMetastatic colorectalMicrosatellite instabilityRAS status

Identifiers

PMID37608030
OpenAlexW4386053699

What OpenQuestion holds

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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.