他莫昔芬减量:减少不良反应的有效策略?

IF 13 1区 医学 Q1 PHARMACOLOGY & PHARMACY Drugs Pub Date : 2024-04-01 Epub Date: 2024-03-14 DOI:10.1007/s40265-024-02010-x
Sanne M Buijs, Stijn L W Koolen, Ron H J Mathijssen, Agnes Jager
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引用次数: 0

摘要

他莫昔芬是雌激素受体阳性乳腺癌辅助治疗的基石,可显著降低乳腺癌复发率和乳腺癌死亡率;然而,其每日 20 毫克的标准辅助剂量因其广泛的不良反应而面临挑战,导致停药率居高不下。降低他莫昔芬的剂量可能是减少治疗相关毒性的一种选择,但目前尚缺乏大型随机对照试验来研究低剂量他莫昔芬在辅助治疗中的耐受性,更重要的是其疗效。我们进行了广泛的文献检索,以探索减少他莫昔芬剂量的耐受性和临床疗效方面的证据。在这篇综述中,我们讨论了有关低剂量他莫昔芬的两个重要主题:(1)使用低剂量他莫昔芬的妇女的不良反应发生率和生活质量;(2)在预防性治疗中通过测量几种疗效衍生物来评估低剂量他莫昔芬的临床疗效。此外,还提供了在辅助治疗中减少他莫昔芬剂量的实用工具,并讨论了为个体患者制定最佳剂量策略的进一步研究。
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Tamoxifen Dose De-Escalation: An Effective Strategy for Reducing Adverse Effects?

Tamoxifen, a cornerstone in the adjuvant treatment of estrogen receptor-positive breast cancer, significantly reduces breast cancer recurrence and breast cancer mortality; however, its standard adjuvant dose of 20 mg daily presents challenges due to a broad spectrum of adverse effects, contributing to high discontinuation rates. Dose reductions of tamoxifen might be an option to reduce treatment-related toxicity, but large randomized controlled trials investigating the tolerability and, more importantly, efficacy of low-dose tamoxifen in the adjuvant setting are lacking. We conducted an extensive literature search to explore evidence on the tolerability and clinical efficacy of reduced doses of tamoxifen. In this review, we discuss two important topics regarding low-dose tamoxifen: (1) the incidence of adverse effects and quality of life among women using low-dose tamoxifen; and (2) the clinical efficacy of low-dose tamoxifen examined in the preventive setting and evaluated through the measurement of several efficacy derivatives. Moreover, practical tools for tamoxifen dose reductions in the adjuvant setting are provided and further research to establish optimal dosing strategies for individual patients are discussed.

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来源期刊
Drugs
Drugs 医学-毒理学
CiteScore
22.70
自引率
0.90%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Drugs is a journal that aims to enhance pharmacotherapy by publishing review and original research articles on key aspects of clinical pharmacology and therapeutics. The journal includes: Leading/current opinion articles providing an overview of contentious or emerging issues. Definitive reviews of drugs and drug classes, and their place in disease management. Therapy in Practice articles including recommendations for specific clinical situations. High-quality, well designed, original clinical research. Adis Drug Evaluations reviewing the properties and place in therapy of both newer and established drugs. AdisInsight Reports summarising development at first global approval. Moreover, the journal offers additional digital features such as animated abstracts, video abstracts, instructional videos, and podcasts to increase visibility and educational value. Plain language summaries accompany articles to assist readers with some knowledge of the field in understanding important medical advances.
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