Desvenlafaxine as a Potential First-Line Treatment for Major Depressive Disorder: A Comprehensive Review and Consensus-Based Clinical Perspective on Efficacy, Safety and Patient Selection Profiles.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2026-09-01 Epub Date: 2026-07-06 DOI:10.1007/s40261-026-01576-6
Claudia Carmassi, Christoph U Correll, Javier de Diego-Adeliño, Antonio Vian-Lains, Ciro Oliveira, Alex Schneider-Pérez, Vikas Mohan Sharma
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引用次数: 0

Abstract

Major depressive disorder is a leading cause of disability worldwide, with significant challenges in treatment response, adherence and functional recovery. Despite the availability of numerous antidepressants, a substantial proportion of patients fail to achieve remission with initial therapy, underscoring the need for effective first-line treatment options. Desvenlafaxine, a serotonin-noradrenaline reuptake inhibitor, has demonstrated efficacy and safety in major depressive disorder, while its pharmacokinetic properties result in minimal drug-drug interactions. This narrative review evaluates clinical evidence supporting the use of desvenlafaxine as a first-line treatment and examines patient subgroups that may benefit most from this antidepressant. A comprehensive literature review was conducted to evaluate the evidence on desvenlafaxine in the treatment of major depressive disorder. This was supplemented by clinical insights discussed during a virtual advisory board meeting held on 16 December, 2024, attended by the authors-psychiatrists from Italy, Germany, Spain, Ireland and Portugal-together with representatives from Neuraxpharm, who market desvenlafaxine. The available evidence suggests that desvenlafaxine offers early symptom relief, sustained efficacy across diverse major depressive disorder symptom clusters, and benefits for patients with anhedonia, fatigue, cognitive dysfunction and functional impairment. Its tolerability and safety profile, including a lower risk of weight gain and drug-drug interactions, contributes to its ease of use and improved adherence. Based on the authors' clinical consensus, desvenlafaxine may be particularly suitable for working-age adults, perimenopausal and menopausal women, those with general medical comorbidities or polypharmacy concerns, and individuals requiring an antidepressant with a broad mechanism of action. In addition, its predictable pharmacokinetics make it a practical choice in primary care settings. While most current guidelines typically recommend selective serotonin reuptake inhibitors as first-line treatment, the favourable tolerability profile and efficacy of desvenlafaxine across diverse symptom clusters may support its consideration as a first-line option in select patient populations.

地文拉法辛作为潜在的一线治疗重度抑郁症:疗效、安全性和患者选择概况的综合评价和基于共识的临床观点
重度抑郁症是世界范围内致残的主要原因,在治疗反应、依从性和功能恢复方面面临重大挑战。尽管有许多抗抑郁药可用,但相当大比例的患者无法通过初始治疗获得缓解,这强调了有效的一线治疗选择的必要性。Desvenlafaxine是一种5 -羟色胺-去甲肾上腺素再摄取抑制剂,已被证明对重度抑郁症有效且安全,而其药代动力学特性导致最小的药物-药物相互作用。这篇叙述性综述评估了支持使用地文拉法辛作为一线治疗的临床证据,并检查了可能从这种抗抑郁药中获益最多的患者亚组。对地文拉法辛治疗重度抑郁症的证据进行了全面的文献综述。在2024年12月16日举行的虚拟咨询委员会会议上,作者——来自意大利、德国、西班牙、爱尔兰和葡萄牙的精神病学家——以及销售desvenlafaxine的Neuraxpharm的代表参加了会议,讨论了临床见解。现有证据表明,地文拉法辛可提供早期症状缓解,对多种重度抑郁症症状群持续有效,并对快感缺乏、疲劳、认知功能障碍和功能障碍患者有益。其耐受性和安全性,包括较低的体重增加风险和药物-药物相互作用,有助于其易于使用和改善依从性。根据作者的临床共识,地文拉法辛可能特别适用于工作年龄的成年人、围绝经期和绝经期妇女、有一般医学合并症或多种药物问题的人,以及需要具有广泛作用机制的抗抑郁药的人。此外,其可预测的药代动力学使其成为初级保健机构的实际选择。虽然目前大多数指南通常推荐选择性5 -羟色胺再摄取抑制剂作为一线治疗,但地文拉法辛在不同症状群中的良好耐受性和疗效可能支持将其作为特定患者群体的一线选择。
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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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