Evidence map›Paper›PMID 36161271›Full record

ArticleInternational journal of cancer2023

Survival outcomes of metastatic breast cancer patients by germline BRCA1/2 status in a large multicenter real-world database.

Audrey Mailliez, Veronique D'Hondt, Amelie Lusque, Olivier Caron, Luc Cabel, Anthony Goncalves, Marc Debled, Laurence Gladieff, Jean-Marc Ferrero, Thierry Petit and 12 more

Registry-linked trialOpen access · hybridAbstract readMulticenter Study
In one paragraph

Article in International journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03275311 (Epidemiological Strategy and Medical Economic), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% 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.

NCT03275311 recruitingnot on this map

Epidemiological Strategy and Medical Economic (ESME) Research Program / Academic Real World Database: Evolution of the Therapeutic Care in Metastatic Breast Cancer Across the French Comprehensive Cancer Centers From 2008

TypeobservationalSponsorUNICANCERRan2014 to 2027Enrolled42,000ConditionsMetastatic Breast Cancer
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. GermlineCancers · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Germline DNA Damage Repair Variants and Prognosis of Patients with High-Risk or Metastatic Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  8. Article
  9. Article
  10. 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

22 authors at 19 institutions in 1 country.

Audrey MailliezCenter Oscar Lambret, Lille, France.ORCID 0000-0002-0475-8631
Veronique D'HondtInstitut régional du Cancer Montpellier/Val d'Aurelle, Montpellier, France.
Amelie LusqueInstitut Claudius Regaud, IUCT-Oncopole, Toulouse, France.
Olivier CaronInstitut Gustave Roussy, Villejuif, France.
Luc CabelInstitut Curie, Paris et Saint Cloud, France.ORCID 0000-0001-5515-9180
Anthony GoncalvesInstitut Paoli-Calmette, Marseille, France.
Marc DebledInstitut Bergonié, Bordeaux, France.
Laurence GladieffInstitut Claudius Regaud, IUCT-Oncopole, Toulouse, France.
Jean-Marc FerreroCenter Antoine Lacassagne, Nice, France.
Thierry PetitCenter Paul Strauss, Strasbourg, France.
Marie Ange Mouret-ReynierCenter Jean Perrin, Clermont Ferrand, France.
Jean-Christophe EymardInstitut Jean Godinot, Reims, France.
Christelle LevyCenter François Baclesse, Caen, France.
Lionel UwerInstitut de Cancerologie de Lorraine, Vandoeuvre-lès-Nancy, France.
Marianne LeheurteurCenter Henri Becquerel, Rouen, France.
Isabelle DesmoulinsCenter Georges François Leclerc, Dijon, France.
Thomas BachelotCenter Léon Bérard, Lyon, France.
Jean-Sebastien FrenelInstitut de cancérologie de l'Ouest, Nantes et Angers, France.
Thibault de la Motte RougeCenter Eugène Marquis, Rennes, France.
Gaëtane SimonUnicancer, Paris, France.
William JacotInstitut régional du Cancer Montpellier/Val d'Aurelle, Montpellier, France.ORCID 0000-0001-7834-061X
Suzette DelalogeInstitut Gustave Roussy, Villejuif, France.
Institut Claudius Regaud · FRInstitut de Recherche en Cancérologie de Montpellier · FRInstitut Gustave Roussy · FRCentre Antoine Lacassagne · FRCentre Eugène Marquis · FRCentre François Baclesse · FRCentre Georges François Leclerc · FRCentre Jean Perrin · FRCentre Léon Bérard · FRCentre Oscar Lambret · FREurométropole de Strasbourg · FRInstitut Bergonié · FRInstitut Curie · FRInstitut de Cancérologie de Lorraine · FRInstitut de Cancérologie de l'Ouest · FRInstitut Jean Godinot · FRInstitut Paoli-Calmettes · FRLaboratoire National Henri Becquerel · FRUniCancer Group · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The outcomes and best treatment strategies for germline BRCA1/2 mutation (gBRCAm) carriers with metastatic breast cancer (MBC) remain uncertain. We compared the overall survival and the first line progression free survival (PFS1) of patients with a gBRCAm identified at initiation of first-line treatment with those of BRCA wild-type (WT) and not-tested (NT) individuals in the ESME real-world database of MBC patients between 2008 and 2016 (NCT03275311). Among the 20 624 eligible patients, 325 had a gBRCAm, 1138 were WT and 19 161 NT. Compared with WT, gBRCAm carriers were younger, and had more aggressive diseases. At a median follow-up of 50.5 months, median OS was 30.6 (95%CI: 21.9-34.3), 35.8 (95%CI: 32.2-37.8) and 39.3 months (95% CI: 38.3-40.3) in the gBRCAm, WT and NT subgroups, respectively. Median PFS1 was 7.9 (95%CI: 6.6-9.3), 7.8 (95%CI: 7.3-8.5) and 9.7 months (95%CI, 9.5-10.0). In the multivariable analysis conducted in the whole cohort, gBRCAm status had however no independent prognostic impact on OS and PFS1. Though, in the triple-negative subgroup, gBRCAm patients had better OS and PFS1 (HR vs WT = 0.76; 95%CI: 0.60-0.97; P = .027 and 0.69; 95% CI: 0.55-0.86; P = .001, respectively). In contrast, in patients with HR+/HER2 negative cancers, PFS1 appeared significantly and OS non significantly lower for gBRCAm carriers (PFS1: HR vs WT = 1.23; 95%CI: 1.03-1.46; P = .024; OS:HR = 1.22, 95% CI: 0.97-1.52, P = .089). In conclusion, gBRCA1/2 status appears to have divergent survival effects in MBC according to IHC subtype.

Indexed as

Breast NeoplasmsBRCA1 ProteinBRCA2 ProteinFemaleHumansPrognosisProgression-Free SurvivalBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humangermline BRCA mutationmetastatic breast cancerreal worldsurvival

Identifiers

PMID36161271
PMCPMC10092337
OpenAlexW4297242573

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.