Tolerance and toxicity of the PARP inhibitor olaparib in older women with epithelial ovarian cancer Journal Article


Authors: Dockery, L. E.; Tew, W. P.; Ding, K.; Moore, K. N.
Article Title: Tolerance and toxicity of the PARP inhibitor olaparib in older women with epithelial ovarian cancer
Abstract: Objectives The objective of this study was to determine the overall tolerability and toxicity of olaparib capsules among older (≥ 65 years) patients with recurrent ovarian cancer treated on 8 completed prospective trials of olaparib. Methods An ancillary data analysis of 398 patients with recurrent ovarian cancer enrolled on eight prospective trials of olaparib capsules was performed. Patients aged 65 years and older were stratified into age groups by 5 year increments (ages 65–69, 70–74, ≥ 75 years) and compared to those < 65. Analysis was restricted to those patients receiving the recommended treatment dose of 400 mg PO b.i.d. Results Of the 398 patients included, 78 were ≥ 65 (age 65–69 n = 38, age 70–74 n = 23, age ≥ 75 n = 17). The majority of elderly patients were Caucasian (n = 2 Asian) and had received ≥ 5 prior lines of chemotherapy. In patients < 65, 46.9% required dose reduction as compared to 44.7% of patients 65–69 years, 47.8% of patients 70–74 years, and 64.7% of patients ≥ 75 years (p = 0.62). In patients < 65 years 41.2% required dose interruption, as compared to 50%, 43.5%, and 64.7% of patients aged 65–69, 70–74, and ≥ 75, respectively (p = 0.11). There were no occurrences of myelodysplastic syndrome or acute myeloid leukemia in any of the older cohorts. Toxicities, including grade 3/4 nausea, were similar across age groups. Conclusions Tolerability and toxicity of olaparib capsules is similar between women ≥ 65 years and < 65 years of age treated for advanced recurrent ovarian cancer. Use of olaparib should be considered in this patient population. © 2017 Elsevier Inc.
Keywords: cancer chemotherapy; controlled study; aged; major clinical study; drug tolerability; fatigue; cancer recurrence; doxorubicin; advanced cancer; drug dose reduction; drug efficacy; drug safety; monotherapy; recommended drug dose; treatment duration; cancer patient; prospective study; prospective studies; neoplasm; ovarian neoplasms; phase 2 clinical trial; neoplasm recurrence, local; anemia; nausea; randomized controlled trial; cohort analysis; randomized controlled trials as topic; age factors; groups by age; age; myelodysplastic syndrome; multicenter study; tumor recurrence; ovary tumor; ovary carcinoma; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor; open study; phase 1 clinical trial; piperazines; piperazine derivative; clinical trials, phase i as topic; clinical trials, phase ii as topic; crossover procedure; double blind procedure; caucasian; olaparib; neoplasms, glandular and epithelial; randomized controlled trial (topic); phthalazine derivative; phthalazines; asian; phase 2 clinical trial (topic); phase 1 clinical trial (topic); acute myeloid leukemia; microcapsule; humans; human; female; priority journal; article; black person; patient history of chemotherapy; poly(adp-ribose) polymerase inhibitors
Journal Title: Gynecologic Oncology
Volume: 147
Issue: 3
ISSN: 0090-8258
Publisher: Elsevier Inc.  
Date Published: 2017-12-01
Start Page: 509
End Page: 513
Language: English
DOI: 10.1016/j.ygyno.2017.10.007
PUBMED: 29037805
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 2 January 2018 -- Source: Scopus
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  1. William P Tew
    226 Tew