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1.
Soins ; 64(841): 56-59, 2019 Dec.
Article in French | MEDLINE | ID: mdl-31864516

ABSTRACT

Le traitement médical des cancers du sein s'est considérablement enrichi ces dernières années z Les indications thérapeutiques ont été affinées grâce à la classification moléculaire des cancers. La chimiothérapie restera encore pour quelques années indispensable notamment pour les cancers du sein triple négatif et surexprimant le récepteur 2 du facteur de croissance épidermique humain. De nouvelles molécules sont en développement pour contourner les mécanismes de résistance à l'hormonothérapie et en association pour en augmenter l'efficacité. L'avenir est aux thérapies ciblées qui visent les anomalies moléculaires de chaque cancer pour chaque patiente.


Subject(s)
Breast Neoplasms/therapy , Female , Forecasting , Humans
2.
Bull Cancer ; 104(5): 485-493, 2017 May.
Article in French | MEDLINE | ID: mdl-28433197

ABSTRACT

Immune checkpoint blockade by the use of anti-PD(L)1 or anti-CTLA4 antibodies can induce long lasting disease response and maybe cure in a lot of advanced cancer patients. This ongoing immunotherapy revolution has given new hope to cancer patients and oncologists. However, still the majority of cancer patients do not respond to immune checkpoint blockade and novel therapeutical possibilities are being tested in several clinical trials. One of the possibilities to enhance responses to immune checkpoint blockade is the combination with chemotherapy or with other immune checkpoint blockade molecules. In this review, we explore the preclinical rational for this synergism and the potential consequences for immunotherapy in oncology.


Subject(s)
Antineoplastic Agents/therapeutic use , Immunotherapy/methods , Neoplasms/therapy , Anthracyclines/therapeutic use , Antigens, Neoplasm/immunology , CTLA-4 Antigen/immunology , Combined Modality Therapy/methods , Cyclophosphamide/therapeutic use , Deoxycytidine/analogs & derivatives , Deoxycytidine/therapeutic use , Humans , Immune Tolerance , Platinum Compounds/therapeutic use , Programmed Cell Death 1 Receptor/immunology , Taxoids/therapeutic use , Gemcitabine
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