Introduction: Ovarian cancer is the most important cause of gynecological cancer-related mortality. Conventional treatments for advanced or recurrent disease offer limited results in terms of long-term responses and survival. Researches have recently focused on target therapies, which represent a new, promising, therapeutic approach, able to maximizing tumor kill and minimizing toxicity. The family of polyadenosine diphosphate-ribose polymerase (PARP) inhibitors is currently one of the most hopeful and investigated alternatives. Areas covered: Preclinical and clinical studies of Olaparib, the most investigated PARP inhibitor in ovarian cancer, are analyzed and discussed. Data were obtained by searching for all English peer-reviewed articles on Medline, on Cochrane Database and all on-going Phase I and II studies registered on National Cancer Institute Clinical Trials; also any related abstracts recently presented on Olaparib at major international congresses will be included. Expert opinion: Bad prognosis and drug resistance usually affect ovarian cancer. Recent trends toward the knowledge of molecular-specific pathways have produced new target drugs. PARP inhibition mediated by Olaparib in BRCA1 (breast cancer 1) and BRCA2 (breast cancer 2)-mutated and in sporadic ovarian cancer represents a promising field of investigation. Further studies are needed to confirm initial exciting results. © 2012 Informa UK, Ltd.

Marchetti, C., Imperiale, L., Gasparri, M. L., Palaia, I., Pignata, S., Boni, T., Bellati, F., Benedetti Panici, P., Olaparib, PARP1 inhibitor in ovarian cancer, <<EXPERT OPINION ON INVESTIGATIONAL DRUGS>>, n/a; 21 (10): 1575-1584. [doi:10.1517/13543784.2012.707189] [http://hdl.handle.net/10807/205549]

Olaparib, PARP1 inhibitor in ovarian cancer

Marchetti, Claudia;
2012

Abstract

Introduction: Ovarian cancer is the most important cause of gynecological cancer-related mortality. Conventional treatments for advanced or recurrent disease offer limited results in terms of long-term responses and survival. Researches have recently focused on target therapies, which represent a new, promising, therapeutic approach, able to maximizing tumor kill and minimizing toxicity. The family of polyadenosine diphosphate-ribose polymerase (PARP) inhibitors is currently one of the most hopeful and investigated alternatives. Areas covered: Preclinical and clinical studies of Olaparib, the most investigated PARP inhibitor in ovarian cancer, are analyzed and discussed. Data were obtained by searching for all English peer-reviewed articles on Medline, on Cochrane Database and all on-going Phase I and II studies registered on National Cancer Institute Clinical Trials; also any related abstracts recently presented on Olaparib at major international congresses will be included. Expert opinion: Bad prognosis and drug resistance usually affect ovarian cancer. Recent trends toward the knowledge of molecular-specific pathways have produced new target drugs. PARP inhibition mediated by Olaparib in BRCA1 (breast cancer 1) and BRCA2 (breast cancer 2)-mutated and in sporadic ovarian cancer represents a promising field of investigation. Further studies are needed to confirm initial exciting results. © 2012 Informa UK, Ltd.
2012
Inglese
Marchetti, C., Imperiale, L., Gasparri, M. L., Palaia, I., Pignata, S., Boni, T., Bellati, F., Benedetti Panici, P., Olaparib, PARP1 inhibitor in ovarian cancer, <<EXPERT OPINION ON INVESTIGATIONAL DRUGS>>, n/a; 21 (10): 1575-1584. [doi:10.1517/13543784.2012.707189] [http://hdl.handle.net/10807/205549]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/205549
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