Evidence map›Paper›PMID 33238394›Full record

ArticlePharmaceuticals (Basel, Switzerland)2020

VEGF-Related Germinal Polymorphisms May Identify a Subgroup of Breast Cancer Patients with Favorable Outcome under Bevacizumab-Based Therapy-A Message from COMET, a French Unicancer Multicentric Study.

Jocelyn Gal, Gérard Milano, Patrick Brest, Nathalie Ebran, Julia Gilhodes, Laurence Llorca, Coraline Dubot, Gilles Romieu, Isabelle Desmoulins, Etienne Brain and 10 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01745757 (Cohort Study of Prospective Validation of Predictive Factors and Biological Imaging of Response to Bevacizumab), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 30% 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.

NCT01745757 completednot on this map

Cohort Study of Prospective Validation of Predictive Factors and Biological Imaging of Response to Bevacizumab (AVASTIN ®) in Combination With Weekly Paclitaxel Chemotherapy in First Line Treatment Patients With Metastatic Breast Cancer

TypeobservationalSponsorUNICANCERRan2012 to 2022Enrolled510ConditionsMetastatic, Breast CancerArmsBevacizumab, paclitaxel
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Genophenotypic Factors and Pharmacogenomics in Adverse Drug Reactions.International journal of molecular sciences · 2021
    Review
  8. 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

20 authors at 10 institutions in 1 country.

Jocelyn GalEpidemiology and Biostatistics Department, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.ORCID 0000-0002-1802-118X
Gérard MilanoCancer Pharmacogenetics and Radiogenetics Unit (UPRC) 7497, Centre Antoine Lacassagne, University Côte d'Azur, 33 avenue de Valombrose, 06100 Nice, France.
Patrick BrestScientific Research National Center (CNRS), Inserm, Ircan, FHU-Oncoage, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.ORCID 0000-0002-1252-4747
Nathalie EbranOncopharmacology Unit, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.
Julia GilhodesDepartment of Biostatistics, Institut Claudius Regaud, IUCT Oncopole, 31300 Toulouse, France.
Laurence LlorcaOncopharmacology Unit, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.
Coraline DubotMedical Oncology Department, Institut Curie, St Cloud, 92210 Paris, France.
Gilles RomieuMedical Oncology Department, Centre Val d'Aurelle-Paul Lamarque, 34298 Montpellier, France.
Isabelle DesmoulinsMedical Oncology Department, Centre Georges François Leclerc, 2100 Dijon, France.
Etienne BrainMedical Oncology Department, Institut Curie, St Cloud, 92210 Paris, France.ORCID 0000-0003-0881-9371
Anthony GoncalvesMedical Oncology Department, Institut Paoli-Calmettes, 13900 Marseille, France.ORCID 0000-0001-7570-7439
Jean-Marc FerreroMedical Oncology Department, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.
Paul-Henri CottuMedical Oncology Department, Institut Curie, St Cloud, 92210 Paris, France.ORCID 0000-0001-6434-3932
Marc DebledMedical Oncology Department, Institut Bergonie, 33000 Bordeaux, France.
Olivier TredanMedical Oncology Department, Centre Leon Berard, 69008 Lyon, France.
Emmanuel ChamoreyEpidemiology and Biostatistics Department, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.
Marco Carlo MerlanoOncology Department, S. Croce & Carle Teaching Hospital, 12100 Cuneo, Italy.
Jérôme LemonnierResearch & Development Departement, Unicancer, 94270 Paris, France.
Marie-Christine Etienne-GrimaldiOncopharmacology Unit, Centre Antoine Lacassagne, University Côte d'Azur, 06100 Nice, France.
Jean-Yves PiergaMedical Oncology Department, Institut Curie, St Cloud, 92210 Paris, France.
Université Côte d'Azur · FRInstitut Curie · FRCEA Valduc · FRCentre Georges François Leclerc · FRCentre Léon Bérard · FRCentre National de la Recherche Scientifique · FRInstitut Bergonié · FRInstitut Claudius Regaud · FRInstitut Paoli-Calmettes · FRUniCancer Group · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prospective multicenter COMET trial followed a cohort of 306 consecutive metastatic breast cancer patients receiving bevacizumab and paclitaxel as first-line chemotherapy. This study was intended to identify and validate reliable biomarkers to better predict bevacizumab treatment outcomes and allow for a more personalized use of this antiangiogenic agent. To that end, we aimed to establish risk scores for survival prognosis dichotomization based on classic clinico-pathological criteria combined or not with single nucleotide polymorphisms (SNPs). The genomic DNA of 306 patients was extracted and a panel of 13 SNPs, covering seven genes previously documented to be potentially involved in drug response, were analyzed by means of high-throughput genotyping. In receiver operating characteristic (ROC) analyses, the hazard model based on a triple-negative cancer phenotype variable, combined with specific SNPs in

Indexed as

bevacizumabbreast canceroverall survivalpharmacogeneticsprecision medicineSNPVEGF

Identifiers

PMID33238394
PMCPMC7700430
OpenAlexW3107285588

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.