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Is There Still a Role for Endocrine Therapy Alone in HR+/HER2- Advanced Breast Cancer Patients? Results from the Analysis of Two Data Sets of Patients Treated with High-Dose Fulvestrant as First-Line Therapy in the Real-World Setting: The EVA and GIM-13 AMBRA Studies.
Cazzaniga, Marina Elena; Verusio, Claudio; Ciccarese, Mariangela; Fumagalli, Alberto; Sartori, Donata; Valerio, Maria Rosaria; Airoldi, Mario; Moretti, Gabriella; Ficorella, Corrado; Gianni, Lorenzo; Michelotti, Andrea; Zambelli, Alberto; Febbraro, Antonio; Generali, Daniele; Pistelli, Mirco; Garrone, Ornella; Musolino, Antonino; Vici, Patrizia; Maur, Michela; Mentuccia, Lucia; La Verde, Nicla; Bianchi, Giulia Valeria; Artale, Salvatore; Blasi, Livio; De Laurentiis, Michelino; Atzori, Francesco; Turletti, Anna; Porpiglia, Mauro; Santini, Daniele; Fabi, Alessandra; Gebbia, Vittorio; Schirone, Alessio; Palumbo, Raffaella; Ferzi, Antonella; Frassoldati, Antonio; Scavelli, Claudio; Clivio, Luca; Giordano, Monica; Donadio, Michela; Biganzoli, Laura; Del Mastro, Lucia; Bisagni, Giancarlo; Livi, Lorenzo; Natoli, Clara; Montemurro, Filippo; Riccardi, Ferdinando; Romagnoli, Emanuela; Marchetti, Paolo; Torri, Valter; Pronzato, Paolo.
Afiliación
  • Cazzaniga ME; Research Unit Phase I Trials, ASST Monza, Monza, Italy.
  • Verusio C; Oncology Unit, ASST Monza, Monza, Italy.
  • Ciccarese M; Oncology Unit, ASST della Valle Olona - Presidio Ospedaliero di Saronno, Saronno, Italy.
  • Fumagalli A; Oncology Unit, Ospedale "Vito Fazzi" di Lecce, Lecce, Italy.
  • Sartori D; Oncology Unit, Ospedale Moriggia Pelascini, Gravedona, Italy.
  • Valerio MR; Oncology Unit, AULSS 3, Mirano, Italy.
  • Airoldi M; Oncology Department, Policlinico "Paolo Giaccone", Palermo, Italy.
  • Moretti G; Oncology Unit 2 - Città della Salute e della Scienza di Torino, Turin, Italy.
  • Ficorella C; Oncology Unit, IRCCS Arcispedale S. Maria Nuova, Reggio Emilia, Italy.
  • Gianni L; Dipartimento di Scienze Cliniche Applicate e Biotecnologiche (DISCAB) - Università Degli Studi Dell'Aquila, L'Aquila, Italy.
  • Michelotti A; Oncology Unit Rimini, Azienda USL Romagna, Rimini, Italy.
  • Zambelli A; Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
  • Febbraro A; Oncology Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Generali D; Oncology Unit, Ospedale Sacro Cuore di Gesù, Fatebenefratelli, Benevento, Italy.
  • Pistelli M; Brest Unit, ASST di Cremona, Cremona, Italy.
  • Garrone O; Oncology Unit, AOU Ospedali Riuniti Ancona, Ancona, Italy.
  • Musolino A; Oncology Unit, A.O.S. Croce e Carle Ospedale di Insegnamento, Cuneo, Italy.
  • Vici P; Oncology Unit, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
  • Maur M; Oncology Unit 2, Istituto Nazionale Tumori Regina Elena - IFO, Rome, Italy.
  • Mentuccia L; Oncology Unit, Policlinico University Hospital of Modena, Modena, Italy.
  • La Verde N; Oncology Unit, ASL di Frosinone, Osp. "SS. Trinità", Sora, Italy.
  • Bianchi GV; Oncology Unit, ASST Fatebenefratelli Sacco Presidio Ospedaliero Fatebenefratelli, Milan, Italy.
  • Artale S; Oncology Unit 1, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
  • Blasi L; Oncology Departement, Ospedale di Gallarate, ASST Valle Olona, Gallarate, Italy.
  • De Laurentiis M; Oncology Unit, ARNAS Civico Palermo, Palermo, Italy.
  • Atzori F; National Cancer Institute "Fondazione Giovanni Pascale", Naples, Italy.
  • Turletti A; Research Unit Phase I Trials, ASST Monza, Monza, Italy.
  • Porpiglia M; Oncology Unit, ASST Monza, Monza, Italy.
  • Santini D; Oncology Unit, ASST della Valle Olona - Presidio Ospedaliero di Saronno, Saronno, Italy.
  • Fabi A; Oncology Unit, Ospedale "Vito Fazzi" di Lecce, Lecce, Italy.
  • Gebbia V; Oncology Unit, Ospedale Moriggia Pelascini, Gravedona, Italy.
  • Schirone A; Oncology Unit, AULSS 3, Mirano, Italy.
  • Palumbo R; Oncology Department, Policlinico "Paolo Giaccone", Palermo, Italy.
  • Ferzi A; Oncology Unit 2 - Città della Salute e della Scienza di Torino, Turin, Italy.
  • Frassoldati A; Oncology Unit, IRCCS Arcispedale S. Maria Nuova, Reggio Emilia, Italy.
  • Scavelli C; Dipartimento di Scienze Cliniche Applicate e Biotecnologiche (DISCAB) - Università Degli Studi Dell'Aquila, L'Aquila, Italy.
  • Clivio L; Oncology Unit Rimini, Azienda USL Romagna, Rimini, Italy.
  • Giordano M; Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
  • Donadio M; Oncology Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Biganzoli L; Oncology Unit, Ospedale Sacro Cuore di Gesù, Fatebenefratelli, Benevento, Italy.
  • Del Mastro L; Brest Unit, ASST di Cremona, Cremona, Italy.
  • Bisagni G; Oncology Unit, AOU Ospedali Riuniti Ancona, Ancona, Italy.
  • Livi L; Oncology Unit, A.O.S. Croce e Carle Ospedale di Insegnamento, Cuneo, Italy.
  • Natoli C; Oncology Unit, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
  • Montemurro F; Oncology Unit 2, Istituto Nazionale Tumori Regina Elena - IFO, Rome, Italy.
  • Riccardi F; Oncology Unit, Policlinico University Hospital of Modena, Modena, Italy.
  • Romagnoli E; Oncology Unit, ASL di Frosinone, Osp. "SS. Trinità", Sora, Italy.
  • Marchetti P; Oncology Unit, ASST Fatebenefratelli Sacco Presidio Ospedaliero Fatebenefratelli, Milan, Italy.
  • Torri V; Oncology Unit 1, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
  • Pronzato P; Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
Breast Care (Basel) ; 15(1): 30-37, 2020 Feb.
Article en En | MEDLINE | ID: mdl-32231495
ABSTRACT

BACKGROUND:

Different studies suggest that fulvestrant 500 mg every 28 days (HD-FUL) could be an active treatment in HR+ advanced breast cancer (ABC) patients even treated with aromatase inhibitors in the adjuvant setting. The aim of this analysis is to describe the outcome of ABC patients treated with HD-FUL as first-line treatment in terms of median duration of treatment and the overall response rate in a real-world setting.

METHODS:

For the purpose of the present analysis, we considered two data sets of HR+ ABC patients collected in Italy between 2012 and 2015 (EVA and GIM-13 AMBRA studies).

RESULTS:

Eighty-one and 91 patients have been identified from the two data sets. The median age was 63 years (range 35-82) for the EVA and 57.8 years (range 35.0-82.3) for the AMBRA patients. ORRs were 23.5 and 24.3% in the whole population, 26.9% in the patients with bone only, and 21.8 and 21.4% in those with visceral metastases. The median duration of HD-FUL was 11.6 months (range 1-48) and 12.4 months (range 2.9-70.0) in the two data sets, respectively.

CONCLUSION:

These data suggest that HD-FUL should still continue to play a significant role as first-line therapy in HR+ ABC patients.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2020 Tipo del documento: Article