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1.
Breast ; 54: 286-292, 2020 Dec.
Article de Anglais | MEDLINE | ID: mdl-33242755

RÉSUMÉ

BACKGROUND: This study evaluated efficacy and safety of palbociclib, a CDK4/6 inhibitor, in heavily-pretreated hormone receptor-positive and human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer (mBC) patients during the compassionate use program in Spain from February 2015 to November 2017. PATIENTS AND METHODS: Patient data were collected retrospectively from 35 hospitals in Spain. Patients with HR+/HER2- mBC who had progressed on ≥4 treatments for advanced disease were eligible. RESULTS: A total of 219 patients received palbociclib in combination with aromatase inhibitors (110; 50.2%), fulvestrant (87; 39.7%), tamoxifen (8; 3.6%) or as single agent (10; 4.6%). Mean age of the patients was 58 years; 31 patients (16.1%) were premenopausal and 162 (83.9%) were postmenopausal at the beginning of treatment with palbociclib. Patients had received a median of 3 previous lines of endocrine therapy (ET) for advanced disease. Real-world tumor response (rwTR) and clinical benefit rate were 5.9% (n = 13) and 46.2% (n = 101), respectively. The median real world progression-free survival (rwPFS) was 6.0 months (95% CI 5.7-7.0) and the median overall survival was 19.0 months (95% CI 16.4-21.7). Subgroup analysis revealed a significant difference in median rwPFS in patients treated with palbociclib plus fulvestrant depending on the duration of prior treatment with fulvestrant monotherapy (>6 versus ≤6 months; HR 1.93, 95% CI 1.37-2.73, p < 0.001). The most frequently reported toxicities were neutropenia, asthenia, thrombopenia and anemia. CONCLUSIONS: Palbociclib can be an effective and safe treatment option in patients with heavily pretreated endocrine-sensitive mBC, especially in those with longer PFS to previous ET.


Sujet(s)
Antinéoplasiques hormonaux/administration et posologie , Protocoles de polychimiothérapie antinéoplasique/administration et posologie , Tumeurs du sein/traitement médicamenteux , Fulvestrant/administration et posologie , Pipérazines/administration et posologie , Pyridines/administration et posologie , Inhibiteurs de l'aromatase/administration et posologie , Tumeurs du sein/métabolisme , Tumeurs du sein/mortalité , Essais cliniques à usage compassionnel , Femelle , Humains , Adulte d'âge moyen , Post-ménopause , Préménopause , Survie sans progression , Récepteurs des oestrogènes/métabolisme , Récepteurs à la progestérone/métabolisme , Études rétrospectives , Espagne , Tamoxifène/administration et posologie , Résultat thérapeutique
2.
Dynamis ; 23: 307-39, 2003.
Article de Espagnol | MEDLINE | ID: mdl-14626283

RÉSUMÉ

This article analyses morphological research on sex determination from the late nineteenth-century to the discovery of sex chromosomes and the theory of sex determination by chromosomes. It describes the links between Morphology and Zoology through their development in Germany and North America, as main producer countries. Cytological research, carried ou on a wide spectrum of zoological species, led to an understanding of important problems regarding the number, appearance and behaviour of chromosomes, supporting determinist hypotheses against those defending the importance of environmental or cytoplasmic factors in the control of development.


Sujet(s)
Biologie cellulaire/histoire , Chromosomes sexuels/génétique , Processus de détermination du sexe , Histoire du 19ème siècle , Histoire du 20ème siècle
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