Evidence map›Paper›PMID 36882736›Full record

ArticleBMC medicine2023

Association between progression-free survival and overall survival in women receiving first-line treatment for metastatic breast cancer: evidence from the ESME real-world database.

Coralie Courtinard, Sophie Gourgou, William Jacot, Matthieu Carton, Olivier Guérin, Laure Vacher, Aurélie Bertaut, Marie-Cécile Le Deley, David Pérol, Patricia Marino and 14 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in BMC medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.7field-weighted citation impact, top 6% 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
NCT03676257 completednot on this map

Survival Endpoints for Treatment Evaluation in Subjects Treated for Metastatic Breast Cancer: Contribution of Real-life Databases

TypeobservationalSponsorInstitut BergoniéRan2008 to 2023Enrolled20,033ConditionsMetastatic Breast CancerArmsChemotherapy (exclusive), Endocrine therapy (exclusive), Combination of endocrine therapy and chemotherapy, Chemotherapy and targeted treatment, Combination of endocrine therapy and targeted treatment
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Spotlight onGenes · 2025
    Article
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  6. Article
  7. Lin28/let-7 axis in breast cancer.Molecular biology reports · 2025
    Review
  8. Article
  9. Review
  10. 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

24 authors at 17 institutions in 1 country.

Coralie CourtinardUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, Epicene Team, UMR 1219, 33000, Bordeaux, France.
Sophie GourgouBiometrics Unit, Institut du Cancer de Montpellier, 208 Rue Des Apothicaires, 34298, Montpellier, France.
William JacotUniversity of Montpellier, 163 Rue Auguste Broussonnet, 34090, Montpellier, France.
Matthieu CartonDepartment of Biostatistics, Institut Curie, 35 Rue Dailly, 92210, Saint-Cloud, France.
Olivier GuérinDepartment of Medical Information, Institut de Cancérologie de L'Ouest Nantes & Angers, 15 Rue André Boquel, 49055, Angers, France.
Laure VacherDepartment of Medical Oncology, Centre Jean Perrin, 58 Rue Montalembert, 63011, Clermont Ferrand, France.
Aurélie BertautDepartment of Biometry, Institut de Cancérologie de Bourgogne, 21079, Dijon, France.
Marie-Cécile Le DeleyCentre Oscar Lambret, 3 Rue Frédéric Combemale, 59000, Lille, France.
David PérolDepartment of Biometry, Centre Léon Bérard, 28 Prom. Léa Et Napoléon Bullukian, Lyon, 69008, France.
Patricia MarinoInstitut Paoli-Calmettes, SESSTIM UMR912, 232, Boulevard Sainte-Marguerite, 13009, Marseille, France.
Christelle LevyDepartment of Medical Oncology, Centre François Baclesse, 3 Avenue du Général Harris, 14000, Caen, France.
Lionel UwerMedical Oncology Department, Institut de Cancérologie de Lorraine, 6 Avenue de Bourgogne, 54519, Vandœuvre-lès-Nancy, France.
Geneviève PerrocheauDepartment of Pharmacy, Institut de Cancérologie de L'Ouest Nantes, Bd Professeur Jacques Monod, 44800, Saint-Herblain, France.
Renaud SchiappaDepartment of Biometry, Centre Antoine Lacassagne, 33 Avenue de Valambrose, 06189, Nice, France.
Florence BachelotDepartment of Medical Information, Institut Curie, 26 Rue d'Ulm, 75005, Paris, France.
Damien ParentDepartment of Pharmacy, Institut de Cancérologie Jean-Godinot, 1 Rue du Général Koenig, 51100, Reims, France.
Mathias BretonDepartment of Medical Information, Centre Eugène Marquis, Avenue de La Bataille Flandres-Dunkerque, 35000, Rennes, France.
Thierry PetitDepartment of Medical Oncology, Institut de Cancérologie Strasbourg Europe (ICANS), 17 Rue Albert Calmette, 67200, Strasbourg, France.
Thomas FilleronDepartment of Biometry, Institut Claudius Regaud - IUCT Oncopole, 1 Avenue Irène-Joliot-Curie, 31059, Toulouse, France.
Agnès LoebDepartment of Medical Information, Centre Henri Becquerel, Rue d'Amiens, 76000, Rouen, France.
Simone Mathoulin-PélissierUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, Epicene Team, UMR 1219, 33000, Bordeaux, France.
Mathieu RobainUnicancer, 101 Rue de Tolbiac, 75654, Paris, France.
Suzette DelalogeDepartment of Cancer Medicine, Gustave Roussy Cancer Campus, 114 Rue Edouard Vaillant, 94800, Villejuif, France.
Carine BelleraUniversity of Bordeaux, Inserm, Bordeaux Population Health Research Center, Epicene Team, UMR 1219, 33000, Bordeaux, France. C.bellera@bordeaux.unicancer.fr.
Université de Bordeaux · FRZimmer Biomet (France) · FRInserm · FRInstitut Curie · FRInstitut de Cancérologie de l'Ouest · FRCentre Eugène Marquis · FRCentre François Baclesse · FRCentre Henri BecquerelCentre Jean Perrin · FRCentre Léon Bérard · FRCentre Oscar Lambret · FRInstitut de Cancérologie de Lorraine · FRInstitut de Cancérologie Strasbourg · FRInstitut Gustave Roussy · FRInstitut Jean Godinot · FRUniCancer Group · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverall survival (OS) is the gold standard endpoint to assess treatment efficacy in cancer clinical trials. In metastatic breast cancer (mBC), progression-free survival (PFS) is commonly used as an intermediate endpoint. Evidence remains scarce regarding the degree of association between PFS and OS. Our study aimed to describe the individual-level association between real-world PFS (rwPFS) and OS according to first-line treatment in female patients with mBC managed in real-world setting for each BC subtype (defined by status for both hormone-receptor [HR] expression and HER2 protein expression/gene amplification).

methodsWe extracted data from the ESME mBC database (NCT03275311) which gathers deidentified data from consecutive patients managed in 18 French Comprehensive Cancer Centers. Adult women diagnosed with mBC between 2008 and 2017 were included. Endpoints (PFS, OS) were described using the Kaplan-Meier method. Individual-level associations between rwPFS and OS were estimated using the Spearman's correlation coefficient. Analyses were conducted by tumor subtype.

results20,033 women were eligible. Median age was 60.0 years. Median follow-up duration was 62.3 months. Median rwPFS ranged from 6.0 months (95% CI 5.8-6.2) for HR-/HER2 - subtype to 13.3 months (36% CI 12.7-14.3) for HR + /HER2 + subtype. Correlation coefficients were highly variable across subtypes and first-line (L1) treatments. Among patients with HR - /HER2 - mBC, correlation coefficients ranged from 0.73 to 0.81, suggesting a strong rwPFS/OS association. For HR + /HER2 + mBC patients, the individual-level associations were weak to strong with coefficients ranging from 0.33 to 0.43 for monotherapy and from 0.67 to 0.78 for combined therapies.

conclusionsOur study provides comprehensive information on individual-level association between rwPFS and OS for L1 treatments in mBC women managed in real-life practice. Our results could be used as a basis for future research dedicated to surrogate endpoint candidates.

Indexed as

Breast NeoplasmsAdultDatabases, FactualFemaleGene ExpressionHumansMiddle AgedProgression-Free SurvivalAssociationBreast cancerOverall survivalProgression-free survivalReal-word dataSurrogacy

Identifiers

PMID36882736
PMCPMC9993797
OpenAlexW4323532697

What OpenQuestion holds

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LicenceCC BY
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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.