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聚(ADP-核糖)聚合酶抑制剂治疗的乳腺癌和卵巢癌患者不良事件管理的成本比较:基于3期临床试验的分析

Cost comparison of adverse event management among breast and ovarian cancer patients treated with poly (ADP-ribose) polymerase inhibitors: analysis based on phase 3 clinical trials.

作者信息

Fan Lin, Zhang Yuanyuan, Maguire Peter, Muston Dominic, Monberg Matthew, Earla Jagadeswara Rao, Mihai Adela, Gulati Poonam

机构信息

Health Economics and Decision Science, Merck & Co., Inc, Rahway, NJ, USA.

Health Economics and Evidence Generation, Wickenstones Ltd, Milton Park, Oxfordshire, UK.

出版信息

J Mark Access Health Policy. 2022 Jun 8;10(1):2078474. doi: 10.1080/20016689.2022.2078474. eCollection 2022.

DOI:10.1080/20016689.2022.2078474
PMID:35693379
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9186353/
Abstract

BACKGROUND

The economic impact of adverse events (AEs) for poly (ADP-ribose) polymerase inhibitors (PARPis) in ovarian or breast cancer has not been widely evaluated.

OBJECTIVE

Compare PARPi-related AE management costs from a US payer perspective.

METHODS

The frequency of treatment-related grade 3-4 AEs was obtained from published clinical trials of PARPis for the treatment of advanced ovarian cancer (AOC), platinum-sensitive recurrent ovarian cancer (PSROC), and metastatic breast cancer (MBC). AE management costs per patient (2020 USD) per treatment course were calculated by multiplying the AE unit costs by the frequency of AEs for each arm of each trial. Sensitivity analyses were conducted according to the lower and upper limits of the 95% confidence interval for AE rates and unit costs, respectively. Scenarios were also performed to explore the uncertainty of outcomes.

RESULTS

Total AE management costs in AOC were: $3,904, olaparib; $5,595, olaparib plus bevacizumab; and $12,215, niraparib. In PSROC, total costs were: $3,894, olaparib; $6,001, rucaparib; and $11,492, niraparib, and in MBC: $3,574, olaparib; and $9,489, talazoparib. Hematological toxicities were the key drivers of AE management costs for PARPis.

CONCLUSIONS

The main AEs among PARPis were hematological. Olaparib was associated with lower AE costs compared to other PARPis.

摘要

背景

聚(ADP - 核糖)聚合酶抑制剂(PARPis)用于卵巢癌或乳腺癌时不良事件(AEs)的经济影响尚未得到广泛评估。

目的

从美国医保支付方的角度比较PARPi相关不良事件管理成本。

方法

治疗相关3 - 4级不良事件的发生率取自已发表的PARPis治疗晚期卵巢癌(AOC)、铂敏感复发性卵巢癌(PSROC)和转移性乳腺癌(MBC)的临床试验。每个疗程每位患者的不良事件管理成本(2020美元)通过将不良事件单位成本乘以每个试验各治疗组不良事件的发生率来计算。分别根据不良事件发生率和单位成本的95%置信区间的下限和上限进行敏感性分析。还进行了情景分析以探索结果的不确定性。

结果

AOC中不良事件管理总成本分别为:奥拉帕利3904美元;奥拉帕利联合贝伐单抗5595美元;尼拉帕利12215美元。在PSROC中,总成本分别为:奥拉帕利3894美元;芦卡帕利6001美元;尼拉帕利11492美元;在MBC中:奥拉帕利3574美元;他拉唑帕利9489美元。血液学毒性是PARPis不良事件管理成本的主要驱动因素。

结论

PARPis中的主要不良事件为血液学方面的。与其他PARPis相比,奥拉帕利的不良事件成本较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/86c8ae75563c/ZJMA_A_2078474_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/dc205688440c/ZJMA_A_2078474_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/0561931d2fc8/ZJMA_A_2078474_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/ccfa00ab0a1b/ZJMA_A_2078474_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/86c8ae75563c/ZJMA_A_2078474_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/dc205688440c/ZJMA_A_2078474_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/0561931d2fc8/ZJMA_A_2078474_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/ccfa00ab0a1b/ZJMA_A_2078474_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/9186353/86c8ae75563c/ZJMA_A_2078474_F0004_OC.jpg

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本文引用的文献

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Moving beyond PARP Inhibition: Current State and Future Perspectives in Breast Cancer.超越 PARP 抑制:乳腺癌的现状和未来展望。
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Tolerability of maintenance olaparib in newly diagnosed patients with advanced ovarian cancer and a BRCA mutation in the randomized phase III SOLO1 trial.SOLO1 随机 III 期临床试验中,新诊断的 BRCA 突变晚期卵巢癌患者维持奥拉帕利的耐受性。
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奥拉帕利和他拉唑帕利治疗种系 BRCA 突变型 HER2 阴性转移性乳腺癌的间接治疗比较。
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An Overview of PARP Inhibitors for the Treatment of Breast Cancer.PARP 抑制剂在乳腺癌治疗中的概述。
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PARP Inhibitors: Clinical Relevance, Mechanisms of Action and Tumor Resistance.聚(ADP-核糖)聚合酶抑制剂:临床相关性、作用机制及肿瘤耐药性
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Cost-effectiveness of olaparib as a maintenance treatment for women with newly diagnosed advanced ovarian cancer and BRCA1/2 mutations in the United States.奥拉帕利作为一种维持治疗药物,用于美国新诊断的 BRCA1/2 突变的晚期卵巢癌女性的成本效益分析。
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