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Multicenter Retrospective Observational (Descriptive) Study of Second-line Therapies After Progression to CDK4/6i in Association With Hormone Therapy, in Patients With HR+/HER2- Advanced Breast Cancer (HERMIONE 13)
Description of the choices for second line treatment, in the normal clinical practice of the centers adhering to the Hermione Network, in patients affected by advanced HR+/HER2- breast cancer who progressed after CDK4/6i in association with hormonal therapy.
Multicenter retrospective observational study, describing therapeutic choices as second-line treatment in patients with HR + / HER2- advanced breast cancer in a real world setting, in centers adhering to the Hermione Network. The study involves the analysis of patients with HR + / HER2- advanced breast cancer treated in second line after initial treatment failure with aromatase inhibitor or Fulvestrant + CDK4 / 6i (Palbociclib, Ribociclib or Abemaciclib). Data will be collected from 150 patients with at least one radiological re-evaluation of disease during 2nd-line treatment from 01 January 2016 until 31 December 2020. List of collected information: Patients' characteristics (gender, age at diagnosis, menopausal state); Disease definition at diagnosis (stage, tumour histology, hormonal status); Surgery (date of surgery, type of surgical approach); Neo-adjuvant treatment; Adjuvant treatment; Date of first relapse (and time since the end of adjuvant therapy); Locations of metastases, Biopsy of metastases, Hormonal receptor status; First-line treatment, hormonal therapy, Best response, Cause of treatment end; Second-line treatment, Best response (radiological re-evaluation), Toxicity, Cause of treatment end. Demographics, baseline characteristics (including tumor characteristics) and treatment information will be summarized descriptively. The categorical variables will be presented in the form of frequencies and percentages, while the continuous variables will be presented by mean, standard deviation and minimum and maximum values. A logistic model will be used for the analysis of clinical benefit (categorical variable), while for the analysis of time-to-event indicators a proportional hazard model will be used. For both analyses, the optimal model will be chosen with the method of "backward" selection. A threshold value of 5% will be used to include predictive variables in the model. The estimates derived by the final models will be evaluated using a penalized model for the evaluation of maximal probability, according to the Firth approach.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Clinica Oncologica Aou Ospedali Riuniti
Ancona, Italy
Ospedale Cardinal Massaia Asti
Asti, Italy
Ospedale San Martino
Belluno, Italy
OSPEDALE Sacro Cuore di Gesù - Fatebenefratelli
Benevento, Italy
Spedali Civili Brescia
Brescia, Italy
Ospedale Sant'Anna, San Fermo della Battaglia
Como, Italy
ASST Cremona - Area Donna
Cremona, Italy
ASST VALLE OLONA - Presidio Gallarate - SC Oncologia
Gallarate, Italy
A.S.S.T. Ovest Milanese
Legnano, Italy
Ospedale Civile di Livorno, Azienda USL Toscana Nord Ovest
Livorno, Italy
Start Date
September 24, 2021
Primary Completion Date
January 30, 2024
Completion Date
December 30, 2024
Last Updated
July 25, 2025
254
ACTUAL participants
Lead Sponsor
University of Milano Bicocca
NCT07483307
NCT06625775
Data Source & Attribution
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