Oncology Research and Treatment · 2018 · 24 citations · 12 references
MedicineOncologyPharmacologyChemotherapyMetastasisMolecular OncologyAdjuvant TherapyBreast Cancer OncologyCancer ImmunotherapyHer2-positive Breast CancerHormonal TherapyMetastatic Breast CancerHer2-positive Breast Cancer TherapyHer2-positive Metastatic DiseaseHormone Receptor-positive Breast Cancer TherapyHuman Epidermal Growth Factor Receptor 2-Positive DiseaseHuman Epidermal Growth Factor Receptor 2-Targeted TherapyMetastatic Breast Cancer TreatmentMetastatic Her2-positive Breast CancerSurvival Benefit Assessment
AIM: The purposes of our study were to compare the clinical outcomes of human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (mBC) patients with or without trastuzumab treatment and HER2-negative patients, and to explore factors that might predict the survival benefit associated with trastuzumab treatment in HER2-positive breast cancer. PATIENTS AND METHODS: A total of 421 patients with mBC were analyzed in this retrospective study. All patients had first-line chemotherapy with or without trastuzumab. They were classified into 3 groups according to their HER2 status and trastuzumab treatment: HER2-positive mBC patients with or without trastuzumab treatment and HER2-negative patents. RESULTS: Trastuzumab administration in HER2-positive mBC patients significantly prolonged overall survival (33 vs. 26 months; P = 0.003) and led to a 49.8% reduction in death risk. In the subgroup analysis, HER2-positive patients with hormone receptor (HR)-negative status (29 vs. 17 months; P = 0.000) or visceral metastasis (30 vs. 21 months; P = 0.000) had more survival benefit when treated with trastuzumab. CONCLUSIONS: Trastuzumab administration significantly improved the overall survival in HER2-positive mBC patients, who gained a prognosis comparable to that of patients with HER2-negative disease. HR status and metastasis site might be important surrogate makers that predict survival benefit from trastuzumab-based treatment.
12
M. Elizabeth H. Hammond, Daniel F. Hayes, Mitch Dowsett et al. · Journal of Clinical Oncology · 2010 · 4.3K citations · Full text
Medicine, Cancer Biology, Oncology +14
Luca Gianni, Tadeusz Pieńkowski, Young‐Hyuck Im et al. · The Lancet Oncology · 2011 · 2.4K citations
Medicine, Oncology, Pharmacology +16
Michel Marty, Francesco Cognetti, D Maraninchi et al. · IRIS UNIMORE (University of Modena and Reggio Emilia) · 2005 · 1.6K citations · Full text
Medicine, Oncology, Pharmacology +17