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Cost-effectiveness of PARP inhibitors in malignancies: A systematic review

OBJECTIVES: Poly (ADP-ribose) polymerase inhibitor (PARPi) have become a mainstay for the treatment of BRCA-mutant malignancies. PARPis are likely to be more effective but also bring an increase in costs. Thus, we aimed at evaluating the cost effectiveness of PARPis in the treatment of malignancies....

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Autores principales: Ding, Haiying, He, Chaoneng, Tong, Yinghui, Fang, Qilu, Mi, Xiufang, Chen, Lingya, Xin, Wenxiu, Fang, Luo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9754183/
https://www.ncbi.nlm.nih.gov/pubmed/36520958
http://dx.doi.org/10.1371/journal.pone.0279286
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author Ding, Haiying
He, Chaoneng
Tong, Yinghui
Fang, Qilu
Mi, Xiufang
Chen, Lingya
Xin, Wenxiu
Fang, Luo
author_facet Ding, Haiying
He, Chaoneng
Tong, Yinghui
Fang, Qilu
Mi, Xiufang
Chen, Lingya
Xin, Wenxiu
Fang, Luo
author_sort Ding, Haiying
collection PubMed
description OBJECTIVES: Poly (ADP-ribose) polymerase inhibitor (PARPi) have become a mainstay for the treatment of BRCA-mutant malignancies. PARPis are likely to be more effective but also bring an increase in costs. Thus, we aimed at evaluating the cost effectiveness of PARPis in the treatment of malignancies. METHODS: Studies of cost effectiveness of PARPis were searched from PubMed, Web of Science, and Cochrane Library. Key information was extracted from the identified studies and reviewed. Quality of the included studies was evaluated using Quality of Health Economic Studies (QHES) instrument. Modeling techniques, measurement of parameters and uncertainty analysis were analyzed across studies. Interventions and cost-effectiveness results were reported stratified by patient population. RESULTS: Among the 25 studies identified, we included 17 on ovarian cancer, 2 on breast cancer, 3 on pancreatic cancer, and 3 on prostate cancer that involved olaparib, niraparib, rucaparib, and talazoparib. All studies had a QHES score of above 75. In the maintenance therapy of ovarian cancer, additional administration of olaparib was cost-effective for newly diagnosed patients after first-line platinum-based chemotherapy but was not cost-effective for platinum-sensitive recurrent patients in majority studies. However, the economic value of other PARPis in ovarian cancer as well as all PARPis in other tumors remained controversial. Cost-effectiveness of PARPi was primarily impacted by the costs of PARPi, survival time, health utility and discount rate. Moreover, genetic testing improved the cost-effectiveness of PARPi treatment. CONCLUSIONS: PARPi is potentially cost-effective for patients with ovarian, pancreatic, or prostate cancer. Genetic testing can improve the cost-effectiveness of PARPi.
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spelling pubmed-97541832022-12-16 Cost-effectiveness of PARP inhibitors in malignancies: A systematic review Ding, Haiying He, Chaoneng Tong, Yinghui Fang, Qilu Mi, Xiufang Chen, Lingya Xin, Wenxiu Fang, Luo PLoS One Research Article OBJECTIVES: Poly (ADP-ribose) polymerase inhibitor (PARPi) have become a mainstay for the treatment of BRCA-mutant malignancies. PARPis are likely to be more effective but also bring an increase in costs. Thus, we aimed at evaluating the cost effectiveness of PARPis in the treatment of malignancies. METHODS: Studies of cost effectiveness of PARPis were searched from PubMed, Web of Science, and Cochrane Library. Key information was extracted from the identified studies and reviewed. Quality of the included studies was evaluated using Quality of Health Economic Studies (QHES) instrument. Modeling techniques, measurement of parameters and uncertainty analysis were analyzed across studies. Interventions and cost-effectiveness results were reported stratified by patient population. RESULTS: Among the 25 studies identified, we included 17 on ovarian cancer, 2 on breast cancer, 3 on pancreatic cancer, and 3 on prostate cancer that involved olaparib, niraparib, rucaparib, and talazoparib. All studies had a QHES score of above 75. In the maintenance therapy of ovarian cancer, additional administration of olaparib was cost-effective for newly diagnosed patients after first-line platinum-based chemotherapy but was not cost-effective for platinum-sensitive recurrent patients in majority studies. However, the economic value of other PARPis in ovarian cancer as well as all PARPis in other tumors remained controversial. Cost-effectiveness of PARPi was primarily impacted by the costs of PARPi, survival time, health utility and discount rate. Moreover, genetic testing improved the cost-effectiveness of PARPi treatment. CONCLUSIONS: PARPi is potentially cost-effective for patients with ovarian, pancreatic, or prostate cancer. Genetic testing can improve the cost-effectiveness of PARPi. Public Library of Science 2022-12-15 /pmc/articles/PMC9754183/ /pubmed/36520958 http://dx.doi.org/10.1371/journal.pone.0279286 Text en © 2022 Ding et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ding, Haiying
He, Chaoneng
Tong, Yinghui
Fang, Qilu
Mi, Xiufang
Chen, Lingya
Xin, Wenxiu
Fang, Luo
Cost-effectiveness of PARP inhibitors in malignancies: A systematic review
title Cost-effectiveness of PARP inhibitors in malignancies: A systematic review
title_full Cost-effectiveness of PARP inhibitors in malignancies: A systematic review
title_fullStr Cost-effectiveness of PARP inhibitors in malignancies: A systematic review
title_full_unstemmed Cost-effectiveness of PARP inhibitors in malignancies: A systematic review
title_short Cost-effectiveness of PARP inhibitors in malignancies: A systematic review
title_sort cost-effectiveness of parp inhibitors in malignancies: a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9754183/
https://www.ncbi.nlm.nih.gov/pubmed/36520958
http://dx.doi.org/10.1371/journal.pone.0279286
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