Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift?
Recent data have demonstrated substantial efficacy with poly (ADP-ribose) polymerase (PARP) inhibitors as treatment and/or maintenance therapy in patients with newly diagnosed advanced epithelial ovarian cancer (EOC). Here, we review efficacy and safety results from four recent Phase III trials in n...
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2021
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oai:doaj.org-article:7db2bf1fae0248e4b42864c456b631ad2021-11-25T17:03:39ZMaintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift?10.3390/cancers132257562072-6694https://doaj.org/article/7db2bf1fae0248e4b42864c456b631ad2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/22/5756https://doaj.org/toc/2072-6694Recent data have demonstrated substantial efficacy with poly (ADP-ribose) polymerase (PARP) inhibitors as treatment and/or maintenance therapy in patients with newly diagnosed advanced epithelial ovarian cancer (EOC). Here, we review efficacy and safety results from four recent Phase III trials in newly diagnosed EOC: SOLO1 (olaparib), PAOLA-1 (olaparib in combination with bevacizumab), PRIMA (niraparib), and VELIA (veliparib). The implications of these data for current clinical practice and areas for future research are discussed, including ongoing studies of targeted agents in the newly diagnosed setting. Data from SOLO1, PAOLA-1, PRIMA, and VELIA confirm the benefit of PARP inhibitors (olaparib, niraparib, veliparib) for women with newly diagnosed EOC. The greatest benefit was seen in patients with a <i>BRCA1</i> and/or <i>BRCA2</i> mutation or in the homologous recombination deficiency (HRD)-test positive subgroup. These four well-conducted studies have generated practice-changing data. However, deciding how to apply these results in clinical practice is challenging, and substantial differences in trial design impede cross-trial comparisons. Recent PARP inhibitor approvals (olaparib, niraparib) in the newly diagnosed EOC setting have provided new maintenance treatment options for a broader patient population. The results of these studies call for personalized medicine based on biomarker profile and other factors, including tolerability, cost considerations, and physician and patient preference. Important areas for future research include appropriate use of both BRCA mutation and HRD testing to inform magnitude of PARP inhibitor benefit as well as exploring further options for patients who are HRD-test negative and for those who become PARP inhibitor resistant.Paul DiSilvestroNicoletta ColomboPhilipp HarterAntonio González-MartínIsabelle Ray-CoquardRobert L. ColemanMDPI AGarticlePARP inhibitorovarian cancerBRCA mutationhomologous recombination deficiencyNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5756, p 5756 (2021) |
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PARP inhibitor ovarian cancer BRCA mutation homologous recombination deficiency Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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PARP inhibitor ovarian cancer BRCA mutation homologous recombination deficiency Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Paul DiSilvestro Nicoletta Colombo Philipp Harter Antonio González-Martín Isabelle Ray-Coquard Robert L. Coleman Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift? |
description |
Recent data have demonstrated substantial efficacy with poly (ADP-ribose) polymerase (PARP) inhibitors as treatment and/or maintenance therapy in patients with newly diagnosed advanced epithelial ovarian cancer (EOC). Here, we review efficacy and safety results from four recent Phase III trials in newly diagnosed EOC: SOLO1 (olaparib), PAOLA-1 (olaparib in combination with bevacizumab), PRIMA (niraparib), and VELIA (veliparib). The implications of these data for current clinical practice and areas for future research are discussed, including ongoing studies of targeted agents in the newly diagnosed setting. Data from SOLO1, PAOLA-1, PRIMA, and VELIA confirm the benefit of PARP inhibitors (olaparib, niraparib, veliparib) for women with newly diagnosed EOC. The greatest benefit was seen in patients with a <i>BRCA1</i> and/or <i>BRCA2</i> mutation or in the homologous recombination deficiency (HRD)-test positive subgroup. These four well-conducted studies have generated practice-changing data. However, deciding how to apply these results in clinical practice is challenging, and substantial differences in trial design impede cross-trial comparisons. Recent PARP inhibitor approvals (olaparib, niraparib) in the newly diagnosed EOC setting have provided new maintenance treatment options for a broader patient population. The results of these studies call for personalized medicine based on biomarker profile and other factors, including tolerability, cost considerations, and physician and patient preference. Important areas for future research include appropriate use of both BRCA mutation and HRD testing to inform magnitude of PARP inhibitor benefit as well as exploring further options for patients who are HRD-test negative and for those who become PARP inhibitor resistant. |
format |
article |
author |
Paul DiSilvestro Nicoletta Colombo Philipp Harter Antonio González-Martín Isabelle Ray-Coquard Robert L. Coleman |
author_facet |
Paul DiSilvestro Nicoletta Colombo Philipp Harter Antonio González-Martín Isabelle Ray-Coquard Robert L. Coleman |
author_sort |
Paul DiSilvestro |
title |
Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift? |
title_short |
Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift? |
title_full |
Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift? |
title_fullStr |
Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift? |
title_full_unstemmed |
Maintenance Treatment of Newly Diagnosed Advanced Ovarian Cancer: Time for a Paradigm Shift? |
title_sort |
maintenance treatment of newly diagnosed advanced ovarian cancer: time for a paradigm shift? |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/7db2bf1fae0248e4b42864c456b631ad |
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