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1.
Ann Oncol ; 32(10): 1245-1255, 2021 10.
Article in English | MEDLINE | ID: mdl-34224826

ABSTRACT

BACKGROUND: The phase III CLinical Evaluation Of Pertuzumab And TRAstuzumab (CLEOPATRA) trial established the combination of pertuzumab, trastuzumab and docetaxel as standard first-line therapy for human epidermal growth factor receptor 2 (HER2)-positive locally recurrent/metastatic breast cancer (LR/mBC). The multicentre single-arm PERtUzumab global SafEty (PERUSE) study assessed the safety and efficacy of pertuzumab and trastuzumab combined with investigator-selected taxane in this setting. PATIENTS AND METHODS: Eligible patients with inoperable HER2-positive LR/mBC and no prior systemic therapy for LR/mBC (except endocrine therapy) received docetaxel, paclitaxel or nab-paclitaxel with trastuzumab and pertuzumab until disease progression or unacceptable toxicity. The primary endpoint was safety. Secondary endpoints included progression-free survival (PFS) and overall survival (OS). Prespecified subgroup analyses included subgroups according to taxane, hormone receptor (HR) status and prior trastuzumab. Exploratory univariable analyses identified potential prognostic factors; those that remained significant in multivariable analysis were used to analyse PFS and OS in subgroups with all, some or none of these factors. RESULTS: Of 1436 treated patients, 588 (41%) initially received paclitaxel and 918 (64%) had HR-positive disease. The most common grade ≥3 adverse events were neutropenia (10%, mainly with docetaxel) and diarrhoea (8%). At the final analysis (median follow-up: 5.7 years), median PFS was 20.7 [95% confidence interval (CI) 18.9-23.1] months overall and was similar irrespective of HR status or taxane. Median OS was 65.3 (95% CI 60.9-70.9) months overall. OS was similar regardless of taxane backbone but was more favourable in patients with HR-positive than HR-negative LR/mBC. In exploratory analyses, trastuzumab-pretreated patients with visceral disease had the shortest median PFS (13.1 months) and OS (46.3 months). CONCLUSIONS: Mature results from PERUSE show a safety and efficacy profile consistent with results from CLEOPATRA and median OS exceeding 5 years. Results suggest that paclitaxel is a valid alternative to docetaxel as backbone chemotherapy. Exploratory analyses suggest risk factors that could guide future trial design.


Subject(s)
Breast Neoplasms , Antibodies, Monoclonal, Humanized , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Breast Neoplasms/drug therapy , Breast Neoplasms/genetics , Female , Humans , Neoplasm Recurrence, Local/drug therapy , Receptor, ErbB-2/genetics , Taxoids/therapeutic use , Trastuzumab/adverse effects , Treatment Outcome
2.
Agents Actions ; 31(1-2): 65-71, 1990 Aug.
Article in English | MEDLINE | ID: mdl-2178320

ABSTRACT

Interaction between anti-inflammatory drugs and reactive oxygen metabolites must be considered in the course of pharmacological studies intended to develop new compounds. Effects of indomethacin, aspirin, and 3,5-diisopropylsalicylic acid (3,5-DIPS) and their copper complexes on PMNL oxidative metabolism and the evolution of an acute inflammatory reaction were studied in the rat. Experiments were performed in vitro by assessment of superoxide generation and reduction of chemiluminescence by PMNLs incubated or not (control) in medium containing various concentrations of these compounds. A dose-related decrease of these parameters was observed, however, copper complexes were found to be more effective than their parent drugs or Cu gluconate. Copper complexes were also more effective anti-inflammatory agents than their parent ligands or Cu gluconate when the volume of exudate and number of exudate PMNLs were assessed after induction of pleurisy in rats by injection of isologous serum. It is concluded that modulation of the PMNL oxidative burst by copper complexes offers an accounting for the anti-inflammatory activity of these compounds.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Copper/pharmacology , Neutrophils/metabolism , Salicylates/pharmacology , Animals , Aspirin/pharmacology , Free Radical Scavengers , In Vitro Techniques , Indomethacin/pharmacology , Luminescent Measurements , Male , Neutrophils/drug effects , Oxidation-Reduction , Pleurisy/chemically induced , Pleurisy/physiopathology , Rats , Rats, Inbred Strains , Superoxides/metabolism
3.
Acta Cient Venez ; 41(3): 171-6, 1990.
Article in Spanish | MEDLINE | ID: mdl-2152376

ABSTRACT

Trace elements execute a vital function in the human body, and their requirements increase depending on the individual pathology of each patient. The present work discusses the amounts of ten trace elements that must be given to a patient in a Total Parenteral Nutrition situation, in relation to his pathology and when to start with each trace element to avoid or forestall complications because of the absence of them. Those trace elements in discussion are: Zinc, Copper, Chromium, Selenium, Molybdenum, Manganese, Iodine, Silicon and Cobalt, this last one as an ion as an element of Vitamin B.


Subject(s)
Parenteral Nutrition, Total/standards , Trace Elements/administration & dosage , Humans , Nutritional Requirements , Trace Elements/therapeutic use
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