Efficacy and Safety of Testosterone Replacement in Testicular Cancer Survivors With Treatment-Influenced Hypogonadism: A Systematic Review.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Andrew A Fritz, Justin P Reinert
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引用次数: 0

Abstract

Objective: The objective is to evaluate the efficacy and safety of testosterone supplementation in testicular cancer survivors with treatment-related hypogonadism.

Data sources: This systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) standards and used Embase, PubMed/MEDLINE, Cochrane Central, Web of Science Core Collection, Korean Journal Index, SciELO, and Global Index Medicus to obtain data in June of 2024.

Study selection and data extraction: Analyses evaluating testosterone supplementation in testicular cancer survivors with treatment-induced hypogonadism were included. Any analyses not assessing supplementation in this population or deemed unretrievable were excluded.

Data synthesis: Ten analyses were included for analysis. A total of 332 bilateral or unilateral testicular cancer survivors with treatment-influenced hypogonadism were reviewed, with 238 patients receiving testosterone replacement. Eight of the 10 analyses assessed participants without poor quality-of-life (QOL) metrics, metabolic factors, and bone mineral density (BMD) at baseline and only found a significant benefit in fat distribution metrics with testosterone supplementation. Two analyses evaluated participants with poor QOL metrics or BMD at baseline and showed improvements in QOL or BMD with testosterone supplementation.

Relevance to patient care and clinical practice: There is robust evidence regarding the efficacy and safety of testosterone replacement in hypogonadal individuals but limited evidence specifically evaluating supplementation in testicular cancer survivors with treatment-influenced hypogonadism.

Conclusions: The results suggest testosterone replacement may be beneficial in patients with impaired QOL metrics, metabolic factors, and BMD at baseline; the results also suggest that routine supplementation for all individuals in this patient population lacks efficacy.

治疗影响性腺功能减退症睾丸癌幸存者补充睾酮的有效性和安全性:系统综述。
研究目的目的是评估睾丸癌幸存者补充睾酮治疗相关性腺功能减退症的有效性和安全性:本系统综述根据系统综述和Meta分析首选报告项目(PRISMA)标准进行,使用Embase、PubMed/MEDLINE、Cochrane Central、Web of Science Core Collection、Korean Journal Index、SciELO和Global Index Medicus获取2024年6月的数据:纳入对治疗诱发性腺功能减退的睾丸癌幸存者补充睾酮情况进行评估的分析。任何未评估该人群补充睾酮情况或无法检索的分析均被排除在外:共纳入 10 项分析。共回顾了332例受治疗影响出现性腺功能减退的双侧或单侧睾丸癌幸存者,其中238例患者接受了睾酮替代治疗。10 项分析中的 8 项评估了基线生活质量 (QOL) 指标、代谢因素和骨矿物质密度 (BMD) 不佳的参与者,结果发现补充睾酮后仅在脂肪分布指标方面有显著益处。两项分析评估了基线QOL指标或BMD较差的参与者,结果显示补充睾酮可改善QOL或BMD:关于性腺功能减退患者补充睾酮的有效性和安全性,目前已有可靠的证据,但专门评估睾丸癌幸存者补充睾酮治疗性腺功能减退的证据有限:结论:研究结果表明,睾酮补充剂可能对基线质量、生活质量指标、代谢因素和 BMD 受损的患者有益;研究结果还表明,对这一患者群体中的所有人进行常规补充缺乏疗效。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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