Literature DB >> 27256873

Patient Counseling and Management of Symptoms During Olaparib Therapy for Recurrent Ovarian Cancer.

Kathleen N Moore1, Bradley J Monk2.   

Abstract

UNLABELLED: : Our primary objective is to review the safety and tolerability profile of olaparib, a novel anticancer therapy, and to discuss key considerations for symptom management in patients with advanced ovarian cancer. Olaparib is the first of a new class of anticancer therapies, poly (ADP-ribose) polymerase (PARP) inhibitors that target tumors that have deficits in homologous recombination repair (such as BRCA mutations) by a process known as synthetic lethality. Through this process, neither the deficiency in homologous recombination repair nor PARP inhibition alone is cytotoxic, but the combination of these two conditions leads to cell death. In December 2014, olaparib received accelerated approval by the U.S. Food and Drug Administration (FDA) as monotherapy for patients with known or suspected deleterious germline BRCA-mutated (as detected by an FDA-approved test) advanced ovarian cancer who had been treated with at least three lines of chemotherapy. Most adverse events (AEs) reported during olaparib clinical trials conducted in patients with recurrent ovarian cancer and measurable disease were of grade 2 or less severity according to the National Cancer Institute's Common Terminology Criteria for Adverse Events. Fatigue and gastrointestinal AEs are among the most common in ovarian cancer clinical trials and can be particularly bothersome to patients. We focus on interventions to address these AEs in patients who are candidates for treatment with olaparib and allow them to remain on therapy for as long as clinically indicated. IMPLICATIONS FOR PRACTICE: Olaparib therapy represents a new approach to treating recurrent ovarian cancer. Some associated adverse events can have a substantial effect on quality of life. It is therefore important for patients, caregivers, and health care providers to have realistic expectations and a thorough understanding of the safety and tolerability profile of olaparib to prevent or alleviate key symptoms so that therapy can continue uninterrupted if possible. This report summarizes a practical approach to supportive care for patients receiving olaparib therapy. ©AlphaMed Press.

Entities:  

Keywords:  BRCA mutation; Homologous recombination pathway; Olaparib; Ovarian cancer; Poly(ADP-ribose) polymerase inhibitor (PARP); Toxicities

Mesh:

Substances:

Year:  2016        PMID: 27256873      PMCID: PMC4978548          DOI: 10.1634/theoncologist.2015-0268

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  35 in total

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Authors:  Tarra Evans; Ursula Matulonis
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Journal:  Pharmacol Ther       Date:  2020-05-23       Impact factor: 12.310

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5.  Sharing real-world experiences to optimize the management of olaparib toxicities: a practical guidance from an Italian expert panel.

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Journal:  Support Care Cancer       Date:  2020-02-11       Impact factor: 3.603

6.  Risk of selected gastrointestinal toxicities associated with poly (ADP-ribose) polymerase (PARP) inhibitors in the treatment of ovarian cancer: a meta-analysis of published trials.

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7.  The efficacy and safety of olaparib in the treatment of cancers: a meta-analysis of randomized controlled trials.

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9.  Tolerability of maintenance olaparib in newly diagnosed patients with advanced ovarian cancer and a BRCA mutation in the randomized phase III SOLO1 trial.

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  9 in total

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