Sabino De Placido1, Mario Giuliano1, Francesco Schettini1, Claudia Von Arx2, Giuseppe Buono1, Ferdinando Riccardi3, Daniela Cianniello4, Roberta Caputo4, Fabio Puglisi5, Marta Bonotto6, Alessandra Fabi7, Domenico Bilancia8, Mariangela Ciccarese9, Vito Lorusso10, Andrea Michelotti11, Dario Bruzzese12, Bianca Maria Veneziani13, Mariavittoria Locci14, Michelino De Laurentiis4, Grazia Arpino15. 1. Medical Oncology, Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy. 2. Medical Oncology, Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy; Department of Surgery and Cancer, Imperial College of London, London, UK. 3. Medical Oncology, "A. Cardarelli" Hospital, Naples, Italy. 4. National Cancer Institute Fondazione "G. Pascale", Naples, Italy. 5. Department of Medicine (DAME), University of Udine, Udine, Italy; Department of Clinical Oncology, CRO Aviano National Cancer Institute, Aviano, Italy. 6. Department of Oncology, University Hospital of Udine, Udine, Italy. 7. Division of Medical Oncology, "Regina Elena" National Cancer Institute, Rome, Italy. 8. "San Carlo" Hospital, Potenza, Italy. 9. Oncology Unit, "Vito Fazi" Hospital of Lecce, Lecce, Italy. 10. Operative Unit of Medical Oncology, Oncology Institute of Bari, Bari, Italy. 11. Medical Oncology, "Santa Chiara" Hospital, Pisa, Italy. 12. Department of Epidemiology, University of Naples "Federico II", Naples, Italy. 13. Department of Molecular Medicine and Medical Biotechnologies, University of Naples "Federico II", Naples, Italy. 14. Department of Neuroscience, Reproductive Medicine, Odontostomatology, University of Naples "Federico II", Naples, Italy. 15. Medical Oncology, Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy. Electronic address: grazia.arpino@unina.it.
Abstract
OBJECTIVES: Given their inclusion and exclusion criteria, randomized clinical trials (RCT) might not include a population that truly mirrors real life (RL). This raises concerns about the applicability of RCT results in clinical practice. We evaluated the efficacy of anti-HER2 treatment with pertuzumab combined with trastuzumab and a taxane as first-line treatment for HER2-positive metastatic breast cancer in a RL setting, and compared the safety results obtained in our population versus the experimental cohort of the CLEOPATRA RCT, which led to the approval of this therapy. MATERIALS AND METHODS: Patients treated with trastuzumab, pertuzumab and a taxane were enrolled in this retrospective study. We compared the tumor features and the patients' characteristics of the RL cohort to those of the CLEOPATRA cohort. We also compared the median progression-free survival (PFS) in the RL population versus specific patients' subgroups. RESULTS: RL patients were more frequently HR-positive, less likely to have visceral metastases (P < .001 for both) and had more frequently received (neo)adjuvant hormone therapy or trastuzumab than CLEOPATRA patients (P = .004 and P < .001, respectively). The median number of anti-HER2 cycles was 8 vs 24 and the median number of cycles was 7 vs 8 for docetaxel in the RL versus CLEOPATRA population, respectively. Adverse reactions of all grades were less frequent in RL. Median PFS was 27.8 months in the RL population and the treatment was equally effective in all patients' subgroups. CONCLUSION: This study provides compelling evidence that pertuzumab, trastuzumab and a taxane are effective and safe also in a clinical scenario.
OBJECTIVES: Given their inclusion and exclusion criteria, randomized clinical trials (RCT) might not include a population that truly mirrors real life (RL). This raises concerns about the applicability of RCT results in clinical practice. We evaluated the efficacy of anti-HER2 treatment with pertuzumab combined with trastuzumab and a taxane as first-line treatment for HER2-positive metastatic breast cancer in a RL setting, and compared the safety results obtained in our population versus the experimental cohort of the CLEOPATRA RCT, which led to the approval of this therapy. MATERIALS AND METHODS:Patients treated with trastuzumab, pertuzumab and a taxane were enrolled in this retrospective study. We compared the tumor features and the patients' characteristics of the RL cohort to those of the CLEOPATRA cohort. We also compared the median progression-free survival (PFS) in the RL population versus specific patients' subgroups. RESULTS: RL patients were more frequently HR-positive, less likely to have visceral metastases (P < .001 for both) and had more frequently received (neo)adjuvant hormone therapy or trastuzumab than CLEOPATRA patients (P = .004 and P < .001, respectively). The median number of anti-HER2 cycles was 8 vs 24 and the median number of cycles was 7 vs 8 for docetaxel in the RL versus CLEOPATRA population, respectively. Adverse reactions of all grades were less frequent in RL. Median PFS was 27.8 months in the RL population and the treatment was equally effective in all patients' subgroups. CONCLUSION: This study provides compelling evidence that pertuzumab, trastuzumab and a taxane are effective and safe also in a clinical scenario.
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