Evidence map›Paper›PMID 24847383›Full record

ArticleJournal of Cancer2014

ERCC1, XRCC1 and GSTP1 Single Nucleotide Polymorphisms and Survival of Patients with Colon Cancer Receiving Oxaliplatin-Based Adjuvant Chemotherapy.

Aziz Zaanan, Cécile Dalban, Jean-François Emile, Hélène Blons, Jean-François Fléjou, Claire Goumard, Melek Istanbullu, Claire Calmel, Khalid Alhazmi, Pierre Validire and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  15. Interleukin-16 polymorphisms as new promising biomarkers for risk of gastric cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
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  17. Hsp90 regulates autophagy and plays a role in cancer therapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
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  19. Reversing drug resistance of cisplatin by hsp90 inhibitors in human ovarian cancer cells.International journal of clinical and experimental medicine · 2015
    Article
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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

15 authors at 10 institutions in 1 country.

Aziz Zaanan1. INSERM, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 2. UPMC Univ Paris 06, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 3. Department of Gastroenterology and Digestive Oncology, European Georges Pompidou Hospital, AP-HP, Paris, France; ; 4. Paris Sorbonne Cité, University of Paris Descartes, Paris, France; ; 5. Cancer Research Personalized Medicine (CARPEM), European Georges Pompidou Hospital, AP-HP, Paris, France;
Cécile Dalban6. Department of Biostatistics and Epidemiology, EA4184, Georges François Leclerc Center, Dijon, France;
Jean-François Emile7. Department of Pathology, Ambroise Paré Hospital, AP-HP, Boulogne, France; ; 8. EA4340, University of Versailles, Saint-Quentin-en-Yvelines, Versailles, France;
Hélène Blons4. Paris Sorbonne Cité, University of Paris Descartes, Paris, France; ; 9. Department of Biology, European Georges Pompidou Hospital, AP-HP, Paris, France;
Jean-François Fléjou1. INSERM, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 2. UPMC Univ Paris 06, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 10. Department of Pathology, Saint-Antoine Hospital, AP-HP, Paris, France;
Claire Goumard1. INSERM, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 2. UPMC Univ Paris 06, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France;
Melek Istanbullu1. INSERM, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 2. UPMC Univ Paris 06, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France;
Claire Calmel1. INSERM, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 2. UPMC Univ Paris 06, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France;
Khalid Alhazmi11. Department of Pathology, European Georges Pompidou Hospital, AP-HP, Paris, France;
Pierre Validire12. Department of Pathology, Mutualiste Montsouris Institute, Paris, France;
Christophe Louvet13. Department of Medical Oncology, Mutualiste Montsouris Institute, Paris, France;
Aimery de Gramont14. Department of Medical Oncology, Saint-Antoine Hospital, AP-HP, Paris, France.
Pierre Laurent-Puig4. Paris Sorbonne Cité, University of Paris Descartes, Paris, France; ; 5. Cancer Research Personalized Medicine (CARPEM), European Georges Pompidou Hospital, AP-HP, Paris, France; ; 9. Department of Biology, European Georges Pompidou Hospital, AP-HP, Paris, France;
Julien Taïeb3. Department of Gastroenterology and Digestive Oncology, European Georges Pompidou Hospital, AP-HP, Paris, France; ; 4. Paris Sorbonne Cité, University of Paris Descartes, Paris, France; ; 5. Cancer Research Personalized Medicine (CARPEM), European Georges Pompidou Hospital, AP-HP, Paris, France;
Françoise Praz1. INSERM, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France; ; 2. UPMC Univ Paris 06, UMR_S 938, Saint-Antoine Research Centre, F-75012, Paris, France;
Hôpital Européen Georges-Pompidou · FRInserm · FRInstitute Mutualiste Montsouris · FRSorbonne Université · FRAssistance Publique – Hôpitaux de Paris · FRCentre de Recherche Saint-Antoine · FRCentre Hospitalier Universitaire Dijon Bourgogne · FRDélégation Paris 5 · FRHôpital Ambroise-Paré · FRHôpital Saint-Antoine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile single nucleotide polymorphisms (SNP) in genes involved in DNA repair or drug metabolism have been shown to influence survival of metastatic colon cancer patients treated with FOLFOX, data on adjuvant setting are scarce.

methodsThis study evaluated the correlation between disease-free survival (DFS) of 210 unselected stage III colon cancer patients receiving FOLFOX chemotherapy, and ERCC1-118 (rs11615, c.354T>C), XRCC1-399 (rs25487, c.1196G>A) and GSTP1-105 (rs1695, c.313A>G) polymorphisms. SNP were determined on tumor DNA using a PCR-based RFLP technique.

resultsIn univariate analysis, a trend towards longer DFS was observed for ERCC1 (C/T + T/T) versus (C/C) (HR=2.29; p=0.06), and XRCC1 (A/A) versus (G/G + G/A) (HR=1.61; p=0.16), but not for GSTP1 genotypes; a statistically significant p value was obtained when combining ERCC1 and XRCC1 favorable genotypes (0 versus ≥ 1 favorable genotypes, HR=2.42; p=0.02). After adjustment on tumor stage, lymph node ratio and differentiation grade, multivariate analysis showed that combining ERCC1 and XRCC1 genotypes gave a p value slightly above the threshold for statistical significance (HR=2.03; p=0.06), which was lower than for tumor stage, lymph node ratio or differentiation grade.

conclusionThe association of ERCC1 and XRCC1 polymorphisms may influence the prognosis of stage III colon cancer patients treated with FOLFOX adjuvant chemotherapy. Yet, these findings need to be confirmed in independent prospective studies.

Indexed as

adjuvant FOLFOXcolon cancerERCC1GSTP1.polymorphismXRCC1

Identifiers

PMID24847383
PMCPMC4026996
OpenAlexW2145696262

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.