Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study

Our objective was to assess the safety and efficacy of olaparib in maintenance therapy of BRCA 1-2 mutated, platinum-sensitive, recurrent ovarian carcinoma after the partial or complete response to the second or further lines platinum-based chemotherapy in a real-world setting. We performed a multic...

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Main Authors: Ana Majić, Branka Petrić Miše, Višnja Matković, Ingrid Belac Lovasić, Kristina Katić, Ivana Canjko, Ana Frobe, Žarko Bajić, Eduard Vrdoljak
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Journal of Oncology
Online Access:http://dx.doi.org/10.1155/2020/6423936
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spelling doaj-52a7556fe233409a8eae1f33436bf21d2020-11-25T03:23:44ZengHindawi LimitedJournal of Oncology1687-84501687-84692020-01-01202010.1155/2020/64239366423936Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional StudyAna Majić0Branka Petrić Miše1Višnja Matković2Ingrid Belac Lovasić3Kristina Katić4Ivana Canjko5Ana Frobe6Žarko Bajić7Eduard Vrdoljak8Department of Oncology, University Hospital Center Split, School of Medicine, University of Split, Spinčićeva 1, Split HR-21.000, CroatiaDepartment of Oncology, University Hospital Center Split, School of Medicine, University of Split, Spinčićeva 1, Split HR-21.000, CroatiaDepartment of Gynecologic Oncology, University Hospital Center Zagreb, Petrova 13, Zagreb HR-10.000, CroatiaDepartment of Radiotherapy and Oncology, University Hospital Center Rijeka, Krešimirova 42, Rijeka HR-51.000, CroatiaDepartment of Gynecologic Oncology, University Hospital Center Zagreb, Petrova 13, Zagreb HR-10.000, CroatiaDepartment of Radiotherapy and Oncology, University Hospital Center Osijek, Josipa Huttlera 4, Osijek HR-31.000, CroatiaDepartment of Oncology and Nuclear Medicine, University Hospital Center Sestre Milosrdnice, School of Dental Medicine, University of Zagreb, Zagreb HR-10.000, CroatiaScientific Unit “Dr. Mirko Grmek”, Psychiatric Hospital “Sveti Ivan”, Jankomir 11, Zagreb HR-10.090, CroatiaDepartment of Oncology, University Hospital Center Split, School of Medicine, University of Split, Spinčićeva 1, Split HR-21.000, CroatiaOur objective was to assess the safety and efficacy of olaparib in maintenance therapy of BRCA 1-2 mutated, platinum-sensitive, recurrent ovarian carcinoma after the partial or complete response to the second or further lines platinum-based chemotherapy in a real-world setting. We performed a multicenter, real-world observational population-based cohort study on the whole population of Croatian patients initiated to olaparib maintenance therapy between 2016 and 2020. The primary endpoints were progression-free survival and the discontinuation of treatment because of adverse events. We enrolled the total population of 69 patients with the median (interquartile range; IQR) age of 53 (48–59), 56 (81%) of them with BRCA1 mutation. The median (IQR) follow-up was 16 (9–25) months. Treatment had to be discontinued because of toxicity in 2 (3%) and temporarily interrupted in 14 (20%), while dose was reduced because of toxicity in 18 (26%) of patients. Toxicity of any grade was observed in 61 (88%) patients and toxicity of grade 3 or 4 in 12 (17%). Median progression-free survival was 21 (95% CI 16-not calculable) months from the introduction of olaparib, and the median overall survival was not reached. Our study confirmed efficacy and safety of olaparib as the maintenance therapy of BRCA 1-2 mutated, platinum-sensitive, recurrent ovarian carcinoma. We observed the real-world efficacy and safety comparable to those observed in the randomized controlled trials. We found the interesting observation of better efficacy of 300 mg tablets, compared to 400 mg capsules, an issue that should be addressed on much larger real-world populations.http://dx.doi.org/10.1155/2020/6423936
collection DOAJ
language English
format Article
sources DOAJ
author Ana Majić
Branka Petrić Miše
Višnja Matković
Ingrid Belac Lovasić
Kristina Katić
Ivana Canjko
Ana Frobe
Žarko Bajić
Eduard Vrdoljak
spellingShingle Ana Majić
Branka Petrić Miše
Višnja Matković
Ingrid Belac Lovasić
Kristina Katić
Ivana Canjko
Ana Frobe
Žarko Bajić
Eduard Vrdoljak
Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study
Journal of Oncology
author_facet Ana Majić
Branka Petrić Miše
Višnja Matković
Ingrid Belac Lovasić
Kristina Katić
Ivana Canjko
Ana Frobe
Žarko Bajić
Eduard Vrdoljak
author_sort Ana Majić
title Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study
title_short Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study
title_full Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study
title_fullStr Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study
title_full_unstemmed Olaparib Outcomes in Patients with BRCA 1-2 Mutated, Platinum-Sensitive, Recurrent Ovarian Cancer in Croatia: A Retrospective Noninterventional Study
title_sort olaparib outcomes in patients with brca 1-2 mutated, platinum-sensitive, recurrent ovarian cancer in croatia: a retrospective noninterventional study
publisher Hindawi Limited
series Journal of Oncology
issn 1687-8450
1687-8469
publishDate 2020-01-01
description Our objective was to assess the safety and efficacy of olaparib in maintenance therapy of BRCA 1-2 mutated, platinum-sensitive, recurrent ovarian carcinoma after the partial or complete response to the second or further lines platinum-based chemotherapy in a real-world setting. We performed a multicenter, real-world observational population-based cohort study on the whole population of Croatian patients initiated to olaparib maintenance therapy between 2016 and 2020. The primary endpoints were progression-free survival and the discontinuation of treatment because of adverse events. We enrolled the total population of 69 patients with the median (interquartile range; IQR) age of 53 (48–59), 56 (81%) of them with BRCA1 mutation. The median (IQR) follow-up was 16 (9–25) months. Treatment had to be discontinued because of toxicity in 2 (3%) and temporarily interrupted in 14 (20%), while dose was reduced because of toxicity in 18 (26%) of patients. Toxicity of any grade was observed in 61 (88%) patients and toxicity of grade 3 or 4 in 12 (17%). Median progression-free survival was 21 (95% CI 16-not calculable) months from the introduction of olaparib, and the median overall survival was not reached. Our study confirmed efficacy and safety of olaparib as the maintenance therapy of BRCA 1-2 mutated, platinum-sensitive, recurrent ovarian carcinoma. We observed the real-world efficacy and safety comparable to those observed in the randomized controlled trials. We found the interesting observation of better efficacy of 300 mg tablets, compared to 400 mg capsules, an issue that should be addressed on much larger real-world populations.
url http://dx.doi.org/10.1155/2020/6423936
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