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Updated: Feb 11, 2026

In vivo Imaging and Therapeutic Treatments in an Orthotopic Mouse Model of Ovarian Cancer
Published on: August 17, 2010
Rucaparib: a new treatment option for ovarian cancer
Ilaria Sabatucci1, Giuseppa Maltese1, Stefano Lepori1
1a Department of Gynecologic Oncology , Fondazione IRCCS Istituto Nazionale dei Tumori , Milan , Italy.
Introduction:
Approximately 50% of high-grade serous ovarian cancers present a deficiency in the pathways involved in homologous recombination (HR). PARP inhibitors prevent single-strand DNA damage repair and determine a progression of the defect towards double-strand breaks, which results in a process known as 'synthetic lethality'. Areas covered: In this review, the authors discuss the efficacy and toxicity of rucaparib either as a single agent or as a maintenance treatment for ovarian cancer. This includes the NGS Foundation Medicine evaluation of the role of this drug in the treatment algorithm of ovarian cancer. Moreover, perspectives on the future development of this drug are presented. Expert opinion: The FDA has approved this drug for the treatment of recurrent BRCA-mutated ovarian cancers, which were previously treated with at least two chemotherapies and has accepted the supplemental new drug application for maintenance use in patients who respond to platinum-based chemotherapy via the Prescription Drug User Fee Act (PDUFA) on 6 April 2018. European Medicines Agency (EMA) approval in the same setting is awaited. The possibility of using PARP inhibitors as a maintenance therapy, as a front-line therapy to combat recurrence, and in combination with anti-angiogenic agents and immune-therapies appears to be of particular interest.
Insights
Rucaparib, a PARP inhibitor, shows efficacy in treating ovarian cancer by exploiting homologous recombination deficiencies. It is approved for recurrent BRCA-mutated cases and under review for maintenance therapy.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- High-grade serous ovarian cancers often exhibit homologous recombination (HR) pathway deficiencies.
- PARP inhibitors induce synthetic lethality in HR-deficient tumors by blocking DNA repair.
- Rucaparib is a PARP inhibitor investigated for ovarian cancer treatment.
Purpose of the Study:
- To review the efficacy and toxicity of rucaparib in ovarian cancer.
- To evaluate rucaparib's role in the ovarian cancer treatment algorithm, including NGS Foundation Medicine insights.
- To present future perspectives on rucaparib development.
Main Methods:
- Review of clinical data on rucaparib efficacy and toxicity.
- Analysis of Next-Generation Sequencing (NGS) Foundation Medicine evaluations.
- Discussion of regulatory approvals and future therapeutic strategies.
Main Results:
- Rucaparib is FDA-approved for recurrent BRCA-mutated ovarian cancer post-chemotherapy.
- Supplemental new drug application accepted for maintenance use in platinum-sensitive responders.
- EMA approval for maintenance use is pending.
Conclusions:
- Rucaparib demonstrates significant clinical utility in specific ovarian cancer populations.
- Maintenance therapy with rucaparib holds promise for improving patient outcomes.
- Future research may explore rucaparib in combination therapies and earlier treatment lines.
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