TY - JOUR
T1 - Olaparib, PARP1 inhibitor in ovarian cancer
AU - Marchetti, Claudia
AU - Imperiale, Ludovica
AU - Gasparri, Maria Luisa
AU - Palaia, Innocenza
AU - Pignata, Sandro
AU - Boni, Terenzio
AU - Bellati, Filippo
AU - Benedetti Panici, Pierluigi
PY - 2012
Y1 - 2012
N2 - 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.
AB - 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.
KW - BRCA1/2
KW - Ovarian cancer
KW - Polyadenosine diphosphate-ribose polymerase inhibitors
KW - Target therapy
KW - BRCA1/2
KW - Ovarian cancer
KW - Polyadenosine diphosphate-ribose polymerase inhibitors
KW - Target therapy
UR - http://hdl.handle.net/10807/205549
U2 - 10.1517/13543784.2012.707189
DO - 10.1517/13543784.2012.707189
M3 - Article
SN - 1354-3784
VL - 21
SP - 1575
EP - 1584
JO - Expert Opinion on Investigational Drugs
JF - Expert Opinion on Investigational Drugs
ER -