A retrospective multicentric observational study of trastuzumab emtansine in HER2 positive metastatic breast cancer: A real-world experience

Antonio Russo, Isabella Sperduti, Laura Pizzuti, Valentina Sini, Marina Della Giulia, Maddalena Barba, Federico Piacentini, Vito Lorusso, Agnese Fabbri, Marcello Maugeri-Saccà, Loretta D'Onofrio, Claudia Omarini, Gennaro Ciliberto, Laura Iezzi, Ernesto Rossi, Andrea Botticelli, Maria Mauri, Filippo Greco, Ilaria Bertolini, Paolo MarchettiElisabetta Landucci, Ornella Garrone, Antonio Maria Alberti, Silverio Tomao, Filippo Greco, Andrea Michelotti, Antonino Grassadonia, Barbara Di Cocco, Lucio Laudadio, Luca Moscetti, Katia Cannita, Domenico Sergi, Angelo Fedele Scinto, Paolo Marolla, Francesco Giotta, Teresa Gamucci, Germano Zampa, Luigi Di Lauro, Patrizia Vici, Corrado Ficorella, Vincenzo Adamo, Giuseppe Sanguineti, Andrea Michelotti, Clara Natoli, Alessandra Cassano, Sandro Barni, Daniele Santini, Emanuela Magnolfi, Lucia Mentuccia, Ruggero De Maria, Daniele Santini

Risultato della ricerca: Articlepeer review

25 Citazioni (Scopus)

Abstract

We addressed trastuzumab emtansine (T-DM1) efficacy in HER2+ metastatic breast cancer patients treated in real-world practice, and its activity in pertuzumab-pretreated patients. We conducted a retrospective, observational study involving 23 cancer centres, and 250 patients. Survival data were analyzed by Kaplan Meier curves and log rank test. Factors testing significant in univariate analysis were tested in multivariate models. Median follow-up was 15 months and median T-DM1 treatment-length 4 months. Response rate was 41.6%, clinical benefit 60.9%. Median progression-free and median overall survival were 6 and 20 months, respectively. Overall, no differences emerged by pertuzumab pretreatment, with median progression-free and median overall survival of 4 and 17 months in pertuzumab-pretreated (p=0.13), and 6 and 22 months in pertuzumab-naïve patients (p=0.27). Patients who received second-line T-DM1 had median progression-free and median overall survival of 3 and 12 months (p=0.0001) if pertuzumab-pretreated, and 8 and 26 months if pertuzumab-naïve (p=0.06). In contrast, in third-line and beyond, median progression-free and median overall survival were 16 and 18 months in pertuzumab-pretreated (p=0.05) and 6 and 17 months in pertuzumab-naïve patients (p=0.30). In multivariate analysis, lower ECOG performance status was associated with progression-free survival benefit (p < 0.0001), while overall survival was positively affected by lower ECOG PS (p < 0.0001), absence of brain metastases (p 0.05), and clinical benefit (p < 0.0001). Our results are comparable with those from randomized trials. Further studies are warranted to confirm and interpret our data on apparently lower T-DM1 efficacy when given as second-line treatment after pertuzumab, and on the optimal sequence order.
Lingua originaleEnglish
pagine (da-a)56921-56931
Numero di pagine11
RivistaOncotarget
Volume8
Stato di pubblicazionePublished - 2017

All Science Journal Classification (ASJC) codes

  • Oncology

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