Evidence map›Paper›PMID 40270610›Full record

ArticleFrontiers in oncology2025

Adjuvant systemic therapy in early breast cancer and results of a prospective observational multicenter BRIDE study: patients outcome and adherence to guidelines in cancer clinical practice.

Stefania Gori, Alessandra Fabi, Catia Angiolini, Monica Turazza, Piermario Salvini, Gianluigi Ferretti, Elisabetta Cretella, Lorenzo Gianni, Claudia Bighin, Angela Toss and 20 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

30 authors.

Stefania GoriMedical Oncology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy.
Alessandra FabiPrecision Medicine Unit in Senology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Catia AngioliniBreast Unit and Multidisciplinary Oncology Group, Department of Breast Oncology, AOU Careggi, Florence, Italy.
Monica TurazzaMedical Oncology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy.
Piermario SalviniOncology, Humanitas Gavazzeni, Bergamo, Italy.
Gianluigi FerrettiDivision of Medical Oncology 1, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Elisabetta CretellaMedical Oncology-Azienda Sanitaria dell'Alto Adige, Bolzano, Italy.
Lorenzo GianniOncology-AUSL Romagna Rimini, Rimini, Italy.
Claudia BighinMedical Oncology-IRCCS AOU San Martino IST, Genova, Italy.
Angela TossDepartment of Oncology and Hematology, Azienda Ospedaliero-Universitaria di Modena, Modena, Italy.
Claudio ZamagniMedical Oncology of Senology and Gynecology, IRCCS AOU Bologna, Policlinico Sant'Orsola, Bologna, Italy.
Patrizia ViciUOSD Sperimentazioni Fase IV, IRCCS Istituto Nazionale Tumori Regina Elena, Rome, Italy.
Costanza De RossiMedical Oncology-Ospedale dell'Angelo Azienda ULSS 3 Serenissima, Venice, Italy.
Antonio RussoMedical Oncology, AOU Policlinico P. Giaccone, Palermo, Italy.
Giancarlo BisagniMedical Oncology, Comprehensive Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Alessio SchironeClinical Oncology, Sant'Anna University Hospital, Ferrara, Italy.
Lucia BorgatoDepartment of Oncology, San Bortolo General Hospital, Azienda ULSS8 Berica, Vicenza, Italy.
Anna CarielloMedical Oncology, AUSL Romagna, Ravenna, Italy.
Claudia CappellettiMedical Oncology, Fano Hospital, Fano, Italy.
Roberto BordonaroMedical Oncology, ARNAS Garibaldi Hospital, Catania, Italy.
Saverio CinieriMedical Oncology, Antonio Perrino Hospital, Brindisi, Italy.
Alessandra ModenaMedical Oncology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy.
Matteo ValerioMedical Oncology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy.
Maria Francesca AlvisiLaboratory of Methodology for Clinical Research, Department of Clinical Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Irene De SimoneLaboratory of Methodology for Clinical Research, Department of Clinical Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Francesca GalliLaboratory of Methodology for Clinical Research, Department of Clinical Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Eliana RulliLaboratory of Methodology for Clinical Research, Department of Clinical Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Anna SantoniLaboratory of Methodology for Clinical Research, Department of Clinical Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Matteo VerzèMedical Direction, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy.
Fabrizio NicolisMedical Direction, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Evaluation of every breast cancer (BC) patient by multidisciplinary team and application of guidelines are very important to ensure the best treatment and achieve the best outcome. Methods: The multicenter prospective observational BRIDE study enrolled, from 01/2018 to 02/2021, 1633 BC patients from 19 Italian cancer centers. To evaluate the clinical and biopathological characteristics of BC patients with pathological stage I-II-III treated with surgery followed by adjuvant systemic therapy, type of therapies delivered, outcome and adherence to guidelines, an analysis of 1123 patients out of 1633 patients enrolled in BRIDE study was conducted. Results: The 1123 patients with stage I-II-III BC had a median age of 61.2 years (Q1-Q3: 50.6-71.7); 70.2% were postmenopausal, 92.1% had ECOG PS 0, 68.4% pT1 disease, 70.7% pN0, 91.7% pathological stage I-II; 68.9% underwent conservative breast surgery and 79.8% sentinel lymph node biopsy alone. According to phenotypic subgroup, 80.6% of patients had a HER2-negative/HR-positive, 10.4% HER2-positive/HR-positive, 6.4% triple negative and 2.6% HER2-positive/HR-negative BC. In clinical practice, the phenotypic tumoral subgroup influenced oncologists in the choice of the type of adjuvant systemic therapy (p<0.0001) according to ESMO and AIOM Guidelines. Adjuvant radiotherapy was administered to 85.5% patients undergoing breast-conserving surgery. At the median follow up of 41.4 months (Q1: 35.3 months - Q3: 57.9 months), the DFS at 48 months was 92.8%, with different rates in the phenotypic subgroups. The adherence to AIOM Guidelines in clinical practice was ≥ 70% for the four evaluated quality indicators of treatment process. Discussion: In patients with pathological stage I-II-III BC, the phenotypic subgroup influenced the oncologists' decision on the choice of type of adjuvant systemic therapy, as also indicated by international and national guidelines. In our patients, the DFS rate at 24 and 48 months after surgery was 95.4% and 92.8% respectively. The adherence to the AIOM Guidelines in clinical practice was high but having both quality indicators (shared at international and national level) to evaluate the quality of care in BC and standardized threshold levels to evaluate adherence to guidelines is very important today because this type of evaluation will increase in the coming years.

Indexed as

adherence to guidelineadjuvant systemic therapyearly breast canceroutcomequality indicators

Identifiers

PMID40270610
PMCPMC12016041

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