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促黄体生成素释放激素激动剂在前列腺癌治疗中的实际差异:全方位治疗视角

Practical differences between luteinizing hormone-releasing hormone agonists in prostate cancer: perspectives across the spectrum of care.

作者信息

Meani Davide, Solarić Mladen, Visapää Harri, Rosén Rose-Marie, Janknegt Robert, Soče Majana

机构信息

Hexal AG, Industriestr. 25, D-83607, Holzkirchen, Germany.

Department of Oncology, University Hospital Center Zagreb (KBC Zagreb), Croatia.

出版信息

Ther Adv Urol. 2017 Nov 23;10(2):51-63. doi: 10.1177/1756287217738985. eCollection 2018 Feb.

Abstract

BACKGROUND

Androgen deprivation therapy (ADT) with luteinizing hormone-releasing hormone (LHRH) agonists is well established for the treatment of men with metastatic prostate cancer. As clear differences in efficacy, safety, or tolerability between the available LHRH agonists are lacking, the healthcare management team needs to look to practical differences between the formulations when selecting therapy for their patients. Moreover, as the economic burden of prostate cancer rises alongside earlier diagnosis and improved survival, the possibility for cost savings by using products with specific features is growing in importance.

METHODS

A review was conducted to summarize the information on the different LHRH agonist formulations currently available and offer insight into their relative benefits and disadvantages from the perspectives of physicians, a pharmacist, and a nurse.

RESULTS

The leuprorelin acetate and goserelin acetate solid implants have the advantage of being ready to use with no requirement for refrigeration, whereas powder and microsphere formulations have to be reconstituted and have specific storage or handling constraints. The single-step administration of solid implants, therefore, has potential to reduce labor time and associated costs. Dosing frequency is another key consideration, as administering the injection provides an opportunity for face-to-face interaction between the patient and healthcare professionals to ensure therapy is optimized and give reassurance to patients. Prostate cancer patients are reported to prefer 3- or 6-monthly dosing, which aligns with the monitoring frequency recommended in European Association of Urology guidelines and has been shown to result in reduced annual costs compared with 1-month formulations.

CONCLUSIONS

A number of practical differences exist between the different LHRH agonist preparations available, which may impact on clinical practice. It is important for healthcare providers to be aware and carefully consider these differences when selecting treatments for their prostate cancer patients.

摘要

背景

使用促黄体生成素释放激素(LHRH)激动剂进行雄激素剥夺疗法(ADT)已被广泛用于治疗转移性前列腺癌男性患者。由于现有LHRH激动剂在疗效、安全性或耐受性方面缺乏明显差异,医疗管理团队在为患者选择治疗方案时需要考虑制剂之间的实际差异。此外,随着前列腺癌的经济负担随着早期诊断和生存率的提高而增加,使用具有特定特征的产品来节省成本的可能性变得越来越重要。

方法

进行了一项综述,以总结目前可用的不同LHRH激动剂制剂的信息,并从医生、药剂师和护士的角度深入了解它们的相对优缺点。

结果

醋酸亮丙瑞林和醋酸戈舍瑞林固体植入剂的优点是无需冷藏即可使用,而粉剂和微球制剂则需要重新配制,并且有特定的储存或处理限制。因此,固体植入剂的单步给药有可能减少劳动时间和相关成本。给药频率是另一个关键考虑因素,因为注射给药为患者和医疗专业人员提供了面对面交流的机会,以确保治疗得到优化并让患者放心。据报道,前列腺癌患者更喜欢每3个月或6个月给药一次,这与欧洲泌尿外科学会指南中推荐的监测频率一致,并且已证明与每月给药一次的制剂相比,每年的成本更低。

结论

现有不同LHRH激动剂制剂之间存在一些实际差异,这可能会影响临床实践。医疗服务提供者在为前列腺癌患者选择治疗方案时,了解并仔细考虑这些差异非常重要。

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