Your browser doesn't support javascript.
loading
Prognostic and clinical impact of the endocrine resistance/sensitivity classification according to international consensus guidelines for advanced breast cancer: an individual patient-level analysis from the Mammella InterGruppo (MIG) and Gruppo Italiano Mammella (GIM) studies.
Lambertini, Matteo; Blondeaux, Eva; Bisagni, Giancarlo; Mura, Silvia; De Placido, Sabino; De Laurentiis, Michelino; Fabi, Alessandra; Rimanti, Anita; Michelotti, Andrea; Mansutti, Mauro; Russo, Antonio; Montemurro, Filippo; Frassoldati, Antonio; Durando, Antonio; Gori, Stefania; Turletti, Anna; Tamberi, Stefano; Urracci, Ylenia; Fregatti, Piero; Razeti, Maria Grazia; Caputo, Roberta; De Angelis, Carmine; Sanna, Valeria; Gasparini, Elisa; Agostinetto, Elisa; de Azambuja, Evandro; Poggio, Francesca; Boni, Luca; Del Mastro, Lucia.
Afiliação
  • Lambertini M; Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, University of Genova, Genoa, Italy.
  • Blondeaux E; Department of Medical Oncology, U.O. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Bisagni G; Clinical Epidemiology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Mura S; Department of Oncology and Advanced Technology, Oncology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • De Placido S; Department of Medical Oncology, UOC Oncologia Medica, University Hospital of Sassari, Sassari, Italy.
  • De Laurentiis M; Department of Clinical Medicine and Surgery, University of Naples Federico II, Napoli, Italy.
  • Fabi A; Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione Pascale IRCCS, Napoli, Italy.
  • Rimanti A; Medical Oncology 1, IRCCS Regina Elena National Cancer Institute, Roma, Italy.
  • Michelotti A; ASST Mantova, Azienda Ospedaliera Carlo Poma, Mantova, Italy.
  • Mansutti M; UO Medical Oncology, S. Chiara Hospital, Pisa, Italy.
  • Russo A; Academic Hospital Santa Maria della Misericordia, Udine, Italy.
  • Montemurro F; Ospedale Giaccone, Palermo, Italy.
  • Frassoldati A; Multidisciplinary Outpatient Oncology Clinic, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
  • Durando A; Department of Translational Medicine and for Romagna, Clinical Oncology, S. Anna University Hospital, Ferrara, Italy.
  • Gori S; Breast Unit, Città della Salute e della Scienza, Ospedale S. Anna, Torino, Italy.
  • Turletti A; Medical Oncology, IRCCS Ospedale Sacro Cuore-Don Calabria, Negrar, Verona, Italy.
  • Tamberi S; Medical Oncology, Ospedale Martini ASL Città di Torino, Torino, Italy.
  • Urracci Y; Oncology Department Area Vasta Romagna, Faenza Hospital, Faenza, Italy.
  • Fregatti P; Department of Medical Oncology, Hospital Businco, Cagliari, Italy.
  • Razeti MG; Department of Surgery, UOC Clinica di Chirurgia Senologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Caputo R; Department of Surgical Sciences and Integrated Diagnostic (DISC), School of Medicine, University of Genova, Genoa, Italy.
  • De Angelis C; Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, University of Genova, Genoa, Italy.
  • Sanna V; Department of Medical Oncology, U.O. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Gasparini E; Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione Pascale IRCCS, Napoli, Italy.
  • Agostinetto E; Department of Clinical Medicine and Surgery, University of Naples Federico II, Napoli, Italy.
  • de Azambuja E; Department of Medical Oncology, UOC Oncologia Medica, University Hospital of Sassari, Sassari, Italy.
  • Poggio F; Department of Oncology and Advanced Technology, Oncology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Boni L; Academic Trials Promoting Team, Institut Jules Bordet, and the Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.
  • Del Mastro L; Academic Trials Promoting Team, Institut Jules Bordet, and the Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.
EClinicalMedicine ; 59: 101931, 2023 May.
Article em En | MEDLINE | ID: mdl-37256095
ABSTRACT

Background:

Prior exposure to adjuvant endocrine therapy (ET) and timing to recurrence are crucial factors for first-line treatment choices in patients with hormone receptor-positive/HER2-negative (HR+/HER2-) breast cancer (BC) and in clinical trial eligibility, classifying metastatic HR+/HER2- BC as endocrine sensitive (ES) or primary (1ER)/secondary (2ER) resistant. However, this classification is largely based on expert opinion and no proper evidence exists to date to support its possible prognostic and clinical impact.

Methods:

This analysis included individual patient-level data from 4 adjuvant phase III randomized trials by the Mammella InterGruppo (MIG) and Gruppo Italiano Mammella (GIM) study groups. The impact of endocrine resistance/sensitivity classification on overall survival (mOS, defined as time between date of distant relapse and death) was assessed in both univariate and multivariate Cox proportional hazards models.

Findings:

Between November 1992 and July 2012, 9058 patients were randomized in 4 trials, of whom 6612 had HR+/HER2- BC. Median follow-up was 9.1 years (interquartile range [IQR] 5.6-15.0). In the whole cohort, disease-free survival and OS were 90.4% and 96.6% at 5 years, and 79.1% and 89.4% at 10 years, respectively. The estimated hazard of recurrence raised constantly during the first 15 years from diagnosis, being more pronounced during the first 2 years and less pronounced after year 7. Among the 493 patients with a distant relapse as first disease-free survival event and available date on ET completion, 72 (14.6%), 207 (42.0%) and 214 (43.4%) were classified as having 1ER, 2ER and ES, respectively. Median follow-up from diagnosis of a distant relapse was 3.8 years (IQR 1.6-7.5). Patients with 1ER were significantly more likely to be younger, to have N2/N3 nodal status, grade 3 tumours and to develop visceral metastases. Site of first distant relapse was significantly different between the 3 groups (p = 0.005). In patients with 1ER, 2ER and ES breast cancer, median mOS was 27.2, 38.4 and 43.2 months, respectively (p = 0.03). As compared to patients with ES disease, a higher risk of death was observed in those with 1 ER (adjusted Hazard Ratio [aHR] 1.54; 95% CI 1.03-2.30) and 2ER (aHR 1.17; 95% CI 0.87-1.56) (p = 0.11).

Interpretation:

This large analysis with long-term follow-up provides evidence on the prognostic and clinical impact of the currently adopted endocrine resistance/sensitivity classification in patients with HR+/HER2- advanced BC. This classification may be considered a valid tool to guide clinical decision-making and to design future ET trials in the metastatic setting.

Funding:

AIRC.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article