Intrathecal ziconotide for the treatment of chronic pain: a collection of clinical experiences and literature review.

P De Negri, C Mastronicola
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Abstract

Objective: Despite the wide use of ziconotide in the USA for treating refractory cancer- and noncancer-related pain, this agent is little used in Europe, even if licensed by the European Medicines Agency (EMA). The reason could be attributed to the high, fixed starting dose required for ziconotide, as stated in the EMA Summary of Product Characteristics (SmPC). This dosage recommendation is based on the results of pivotal clinical studies of ziconotide, which utilized aggressive titration schedules. Thus, a reappraisal of the available evidence, as well as a reflection on real-life clinical experiences, might be useful to identify practice adjustments to improve the clinical application of ziconotide in the European scenario. In line with this need, this paper reports some clinical experiences of patients with chronic pain treated with ziconotide intrathecal (IT) therapy in Italy, particularly focusing on long-term treatment to further characterize and improve the use of this agent in real practice. Moreover, a literature review of the available data on the effectiveness and safety of IT ziconotide is provided.

Case series: Collected clinical experiences suggested that the use of IT ziconotide represents a valuable option, particularly in cases where other treatments have been ineffective or poorly tolerated. Ziconotide was shown to not cause severe side effects in the long-term treatment, leading to a constant pain relief effect at stable doses, without adverse events that caused therapy interruption. The overall constant ziconotide dosages also suggest the absence of a tolerance effect. In parallel, the evidence in the literature aligns with real-world evidence and further supports the use of IT ziconotide as an important option for the management of chronic pain.

Conclusions: IT ziconotide represents a valuable addition to the armamentarium of pain management strategies, offering hope for improved quality of life for patients suffering from chronic, treatment-resistant pain. Continued research and clinical experience will further elucidate its optimal use and role in comprehensive pain care.

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鞘内齐考诺肽治疗慢性疼痛:临床经验集和文献综述。
目的:尽管齐科诺肽在美国被广泛用于治疗难治性癌症和非癌症相关疼痛,但在欧洲,即使获得了欧洲药品管理局(EMA)的许可,这种药物也很少被使用。究其原因,正如欧洲药品管理局(EMA)的《产品特性摘要》(SmPC)所述,齐科诺特需要较高的固定起始剂量。这一剂量建议是基于齐科诺肽关键临床研究的结果,这些研究采用了积极的滴定计划。因此,对现有证据的重新评估以及对现实生活中临床经验的反思可能有助于确定实践调整,从而改善齐科诺特在欧洲的临床应用。根据这一需求,本文报告了意大利慢性疼痛患者接受齐科诺特鞘内治疗的一些临床经验,尤其侧重于长期治疗,以进一步描述和改进该药物在实际应用中的使用。此外,还提供了有关 IT 齐酮诺肽有效性和安全性的现有数据的文献综述:收集的临床经验表明,使用 IT 齐酮诺肽是一种有价值的选择,尤其是在其他疗法无效或耐受性差的病例中。研究表明,在长期治疗中,齐科诺肽不会产生严重的副作用,在剂量稳定的情况下可持续缓解疼痛,不会出现导致治疗中断的不良反应。齐科诺肽的总体恒定剂量也表明不存在耐受效应。同时,文献中的证据与现实世界中的证据相吻合,进一步支持使用 IT 齐科诺特作为治疗慢性疼痛的重要选择:IT齐科诺肽是疼痛治疗策略的重要补充,为改善慢性、耐药性疼痛患者的生活质量带来了希望。持续的研究和临床经验将进一步阐明其在综合疼痛治疗中的最佳应用和作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.30
自引率
6.10%
发文量
906
审稿时长
2-4 weeks
期刊介绍: European Review for Medical and Pharmacological Sciences, a fortnightly journal, acts as an information exchange tool on several aspects of medical and pharmacological sciences. It publishes reviews, original articles, and results from original research. The purposes of the Journal are to encourage interdisciplinary discussions and to contribute to the advancement of medicine. European Review for Medical and Pharmacological Sciences includes: -Editorials- Reviews- Original articles- Trials- Brief communications- Case reports (only if of particular interest and accompanied by a short review)
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