曲妥珠单抗- emtansine与曲妥珠单抗治疗伊朗残留侵袭性her -2阳性乳腺癌的成本-效用分析

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Iranian Journal of Pharmaceutical Research Pub Date : 2024-12-17 eCollection Date: 2024-01-01 DOI:10.5812/ijpr-153452
Homa Hemati, Marzieh Nosrati, Meysam Seyedifar
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引用次数: 0

摘要

背景:乳腺癌是女性中最常见的癌症类型之一,其发病率在伊朗呈上升趋势。her -2阳性乳腺癌是侵袭性的,通常伴有较差的预后。这种类型的乳腺癌患者会对曲妥珠单抗等药物产生耐药性。曲妥珠单抗-emtansine (TDM1)是一种用于降低癌细胞对曲妥珠单抗耐药性的药物。TDM1已被证明可以降低乳腺癌的死亡率和复发率。目的:本研究旨在评估TDM1与曲妥珠单抗治疗残留侵袭性her -2阳性乳腺癌的成本-效用,并计算预算影响。方法:建立一个包含四种健康状态的马尔可夫生命视界模型。45岁浸润性残留her -2阳性乳腺癌的女性进入模型。该研究采用了医疗保健系统的视角,报告的成本以2021年的美元计算。成本贴现率为7%,效用价值贴现率为3%。效用值和转移概率来源于已发表的文献。成本是根据指导方针、专家意见和伊朗关税来估算的。伊朗的药物经济学门槛为1085美元,用于比较。计算增量成本-效果比(ICER)和TDM1的预算影响,并进行敏感性分析以评估模型的稳健性。结果:模型显示,TDM1治疗可使患者质量调整生命年(QALY)增加1.59个,额外费用为1408美元。考虑到伊朗1085美元的药物经济学门槛(计算ICER: 886美元/ QALY),这被认为是具有成本效益的。单向敏感性分析显示,该模型对TDM1和曲妥珠单抗的成本、效用值和成本的贴现率以及实现侵袭性无病生存(IDFS)的概率敏感。概率敏感性分析显示,59.61%的模拟低于伊朗药物经济学阈值,支持模型的鲁棒性。预算影响分析显示,与曲妥珠单抗相比,三年期间TDM1治疗所需的额外预算为1,120,546美元。结论:尽管TDM1的成本较高,但在伊朗治疗残留侵袭性her -2阳性乳腺癌方面,TDM1比曲妥珠单抗更具成本效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cost-Utility Analysis of Trastuzumab-Emtansine Versus Trastuzumab for the Treatment of Residual Invasive HER-2-Positive Breast Cancer in Iran.

Background: Breast cancer is one of the most common types of cancer in women, and its incidence is increasing in Iran. HER-2-positive breast cancer is invasive and often associated with poorer outcomes. Patients with this type of breast cancer can develop resistance to medications like trastuzumab. Trastuzumab-emtansine (TDM1) is a medication developed to reduce cancer cell resistance to trastuzumab. The TDM1 has been shown to decrease the incidence of death and recurrence in breast cancer.

Objectives: This study aimed to evaluate the cost-utility and calculate the budget impact of TDM1 versus trastuzumab for the treatment of residual invasive HER-2-positive breast cancer.

Methods: A Markov model with a lifetime horizon was developed, incorporating four health states. Women aged 45 with residual invasive HER-2-positive breast cancer entered the model. The study adopted a healthcare system perspective, with costs reported in 2021 US dollars. Discount rates of 7% for costs and 3% for utility values were applied. Utility values and transition probabilities were derived from published literature. Costs were estimated based on guidelines, expert opinions, and Iranian tariffs. Iran's pharmacoeconomic threshold of 1085$ was used for comparison. The incremental cost-effectiveness ratio (ICER) and budget impact of TDM1 were calculated, and sensitivity analyses were conducted to assess the robustness of the model.

Results: The model indicated that treatment with TDM1 resulted in a 1.59 quality-adjusted life year (QALY) increase, with an additional cost of 1408$. This was deemed cost-effective, considering Iran's pharmacoeconomic threshold of 1085$ (calculated ICER: 886$ per QALY gained). One-way sensitivity analysis revealed that the model was sensitive to the costs of TDM1 and trastuzumab, the discount rates for utility values and costs, and the probability of achieving invasive disease-free survival (IDFS). Probabilistic sensitivity analysis showed that 59.61% of simulations fell below Iran's pharmacoeconomic threshold, supporting the model's robustness. The budget impact analysis revealed that the additional budget required for TDM1 treatment over a three-year period was 1,120,546$ compared to trastuzumab.

Conclusions: Although TDM1 imposes higher costs, it is more cost-effective than trastuzumab for the treatment of residual invasive HER-2-positive breast cancer in Iran.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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