Evidence map›Paper›PMID 37637599›Full record

ArticleCureus2023

HER2 Status in RAS and BRAF Wild-Type Metastatic Colorectal Cancer: A Portuguese Study.

Teresa Fraga, Maria João de Sousa, Joana Magalhães, Raquel Basto, Judy Paulo, Nuno Bonito, José Paulo Magalhães, Paulo Figueiredo, Gabriela M Sousa

Open access · diamondAbstract read
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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 4 institutions in 1 country.

Teresa FragaMedical Oncology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
Maria João de SousaMedical Oncology, Centro Hospitalar Universitário do Porto, Porto, PRT.
Joana MagalhãesMedical Oncology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
Raquel BastoMedical Oncology, Centro Hospitalar Vila Nova de Gaia/Espinho, Gaia, PRT.
Judy PauloMedical Oncology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
Nuno BonitoMedical Oncology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
José Paulo MagalhãesPathology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
Paulo FigueiredoPathology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
Gabriela M SousaMedical Oncology, Instituto Português de Oncologia de Coimbra Francisco Gentil, Coimbra, PRT.
Centro Hospitalar de Vila Nova de Gaia · PTInstituto Português de Oncologia de Coimbra Francisco Gentil · PTInstituto Português de Oncologia de Coimbra Francisco Gentil · PTCentro Hospitalar do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionColorectal cancer (CRC) is the second-most deadly cancer worldwide. However, there remains a scarcity of precision treatments available for this type of cancer. Amplification or overexpression of human epidermal growth factor receptor 2 (HER2+) is a well-established therapeutic target in gastric and breast cancer. HER2 is positive in approximately 5% of CRC cases and has been implicated in resistance to therapy with anti-epidermal growth factor receptor antibodies. The aim of this study was to evaluate HER2 status in RAS and BRAF wild-type metastatic CRC (mCRC) and its correlation with survival outcomes. MATERIALS AND

methodsA single-center retrospective analysis of RAS and BRAF wild-type mCRC patients undergoing systemic treatment was conducted from July 2014 to September 2020. Tissue HER2 status was determined by immunohistochemistry (IHC) and/or fluorescence in situ hybridization (FISH) and/or chromogenic in situ hybridization (CISH). HER2+ was defined as IHC3 (+) or IHC2 (+) through FISH or CISH (+).

resultsFifty-nine patients were included. The median age of all the included patients was 64 years (33-82). Four patients had HER2+ tumors (7%). Four patients had HER2+ tumors (7%). The majority of HER2+ mCRC cases were males (n=3) and left-sided CRC (n=3). All patients received FOLFIRI plus cetuximab as first-line treatment. At the median follow-up of 24.0 months, patients with HER2-negative mCRC presented with a median overall survival (mOS) of 39.4 months (95% confidence interval (CI) 32.7-46.0) and the four patients with HER2+ mCRC had a mOS of 20.4 months (95% CI; 9.5-31.3; p=0.07). In HER2-negative patients, the median PFS (mPFS) was 11.3 months (95% CI; 9.2-13.4) vsHER2-positive patients with a mPFS of 10.9 months (95% CI; 1.3-20.4; p=0.47).

conclusionsTo our knowledge, this is the first study reporting HER2+ in mCRC patients in a Portuguese population and the HER2+ rate was consistent with previous studies. Our study suggests that HER2+ may potentially be a marker that is able to predict poor prognosis in RAS and BRAF wild-type mCRC.

Indexed as

braf mutationcolorectal cancerher2metastaticportugalras

Identifiers

PMID37637599
PMCPMC10460123
OpenAlexW4385363627

What OpenQuestion holds

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LicenceCC BY
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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.