Evidence map›Paper›PMID 24399079›Full record

Trial reportAnnals of oncology : official journal of the European Society for Medical Oncology2014

Characteristics and clinical outcome of T1 breast cancer: a multicenter retrospective cohort study.

G Houvenaeghel, A Goncalves, J M Classe, J R Garbay, S Giard, H Charytensky, M Cohen, C Belichard, C Faure, S Uzan and 13 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Annals of oncology : official journal of the European Society for Medical Oncology, 2014. 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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.0field-weighted citation impact, top 14% 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.

NCT03461172 unknown statusnot on this map

Database of Data Collection in Senological Surgery

TypeobservationalSponsorInstitut Paoli-CalmettesRan2006 to 2026Enrolled50,000ConditionsSurgery of Breast CancerArmsSurgery of breast cancer, Clinical data collection
NCT04248998 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

Targeting Triple Negative BREAst Cancer Metabolism With a Combination of Chemotherapy and a Diet Mimicking FASTing Plus/Minus Metformin in the Preoperative Setting: the BREAKFAST Trial

TypeinterventionalSponsorFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRan2020 to 2024Enrolled30ConditionsTriple-negative Breast CancerArmsFasting-mimicking diet, Metformin, Preoperative chemotherapy
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

23 authors at 13 institutions in 1 country.

G HouvenaeghelDepartment of Surgery, Institut Paoli Calmettes, Aix Marseille Université, Marseilleand CRCM. Electronic address: houvenaeghelg@ipc.unicancer.fr.
A GoncalvesDepartment of Oncology, Institut Paoli Calmettes, Aix Marseille Université, Marseille.
J M ClasseDepartment of Surgery, Institut René Gauducheau, Nantes.
J R GarbayDepartment of Surgery, Institut Gustave Roussy, Villejuif.
S GiardDepartment of Surgery, Centre Oscar Lambret, Lille.
H CharytenskyDepartment of Surgery, Centre Claudius Regaud, Toulouse.
M CohenDepartment of Surgery, Institut Paoli Calmettes, Aix Marseille Université, Marseilleand CRCM.
C BelichardDepartment of Surgery, Centre René Huguenin, Saint Cloud.
C FaureDepartment of Surgery, Centre Léon Bérard, Lyon.
S UzanDepartment of Surgery, Hôpital Tenon, Paris.
D HudryDepartment of Surgery, Centre Georges François Leclerc, Dijon.
P AzuarDepartment of Surgery, Hôpital de Grasse, Grasse.
R VilletDepartment of Surgery, Hôpital des Diaconnesses, Paris.
P GimberguesDepartment of Surgery, Centre Jean Perrin, Clermont Ferrand.
C Tunon de LaraDepartment of Surgery, Institut Bergonié, Bordeaux.
M MartinoDepartment of Surgery, Institut Paoli Calmettes, Aix Marseille Université, Marseilleand CRCM.
E LambaudieDepartment of Surgery, Institut Paoli Calmettes, Aix Marseille Université, Marseilleand CRCM.
C CoutantDepartment of Surgery, Centre Georges François Leclerc, Dijon.
F DravetDepartment of Surgery, Institut René Gauducheau, Nantes.
M P ChauvetDepartment of Surgery, Centre Oscar Lambret, Lille.
E Chéreau EwaldDepartment of Surgery, Institut Paoli Calmettes, Aix Marseille Université, Marseilleand CRCM; Department of Surgery, Hôpital Tenon, Paris.
F Penault-LlorcaDepartment of Pathology, Centre Jean Perrin, Clermont Ferrand.
B EsterniBiostatistic, Department of Surgery, Institut Paoli Calmettes, Marseilleand CRCM, France.
Aix-Marseille Université · FRInstitut Paoli-Calmettes · FRCentre Georges François Leclerc · FRCentre Jean Perrin · FRCentre Oscar Lambret · FRGroupe d'Analyse et de Théorie Economique Lyon St Etienne · FRSorbonne Université · FRCentre Léon Bérard · FRHôpital des Diaconesses · FRHôpital René Huguenin · FRInstitut Bergonié · FRInstitut Claudius Regaud · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA subgroup of T1N0M0 breast cancer (BC) carries a high potential of relapse, and thus may require adjuvant systemic therapy (AST). PATIENTS AND

methodsRetrospective analysis of all patients with T1 BC, who underwent surgery from January 1999 to December 2009 at 13 French sites. AST was not standardized.

resultsAmong 8100 women operated, 5423 had T1 tumors (708 T1a, 2208 T1b and 2508 T1c 11-15 mm). T1a differed significantly from T1b tumors with respect to several parameters (lower age, more frequent negative hormonal status and positive HER2 status, less frequent lymphovascular invasion), exhibiting a mix of favorable and poor prognosis factors. Overall survival was not different between T1a, b or c tumors but recurrence-free survival was significantly higher in T1b than in T1a tumors (P = 0.001). In multivariate analysis, tumor grade, hormone therapy and lymphovascular invasion were independent prognostic factors.

conclusionRelatively poor outcome of patients with T1a tumors might be explained by a high frequency of risk factors in this subgroup (frequent negative hormone receptors and HER2 overexpression) and by a less frequent administration of AST (endocrine treatment and chemotherapy). Tumor size might not be the main determinant of prognosis in T1 BC.

Indexed as

Adjuvants, PharmaceuticBreast NeoplasmsCohort StudiesDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleHumansLymphatic MetastasisNeoplasm Recurrence, LocalNeoplasm StagingReceptors, EstrogenReceptors, ProgesteroneRetrospective StudiesRisk FactorsTreatment OutcomeAdjuvants, PharmaceuticERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, Progesteroneadjuvant systemic therapybreast cancerprognosisT1N0M0

Identifiers

PMID24399079
PMCPMC4433506
OpenAlexW2130334544

What OpenQuestion holds

Textmetadata
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.