# A New Era for Esketamine in Managing Treatment-Resistant Depression: A Systematic Review of Its Use From Adjunct to First-Line Therapy

**Authors:** Srijan Shetty, Balakrishnan Sadasivam

PMC · DOI: 10.7759/cureus.91829 · Cureus · 2025-09-08

## TL;DR

Esketamine, a form of ketamine, shows promise as a treatment for depression that doesn't respond to other therapies, but more research is needed to confirm its effectiveness and proper use.

## Contribution

This paper reviews the emerging role of esketamine from adjunct to potential first-line therapy for treatment-resistant depression.

## Key findings

- Esketamine may act as a rapid-acting standalone therapy for treatment-resistant depression.
- Molecular mechanisms suggest TRD involves glutamatergic dysfunction and neuroinflammation.
- Current evidence is limited, highlighting the need for large-scale trials to confirm therapeutic benefits.

## Abstract

Treatment-resistant depression (TRD) remains a major clinical challenge, affecting nearly one-third of individuals with major depressive disorder (MDD) who fail to respond to standard antidepressant therapies. Esketamine, the S-enantiomer of ketamine, has emerged as a novel therapeutic option. Esketamine, initially introduced as an add-on therapy, has more recently also received recognition for use as a standalone treatment. This review aims to synthesize current clinical evidence on the efficacy and safety of esketamine monotherapy while exploring its molecular mechanisms and identifying research gaps. A systematic literature search was conducted across PubMed, Google Scholar, MedRxiv, and BioRxiv up to March 2025. Although designed as a systematic review, only one qualifying clinical trial was identified, limiting the feasibility of a meta-analysis and underscoring the scarcity of direct evidence. Despite this limitation, molecular insights suggest that TRD is associated with glutamatergic system dysfunction, impaired neuroplasticity, hypothalamic-pituitary-adrenal (HPA) axis abnormalities, and neuroinflammatory processes. Intranasal esketamine demonstrates potential as a rapid-acting and effective standalone therapy for TRD; nevertheless, further robust, large-scale randomized controlled trials are essential to confirm its therapeutic benefit, establish optimal dosing strategies, and overcome current research limitations.

## Linked entities

- **Chemicals:** esketamine (PubChem CID 182137), ketamine (PubChem CID 3821)
- **Diseases:** depression (MONDO:0002050), major depressive disorder (MONDO:0002009)

## Full-text entities

- **Diseases:** Resistant Depression (MESH:D061218), neuroinflammatory (MESH:D000090862), MDD (MESH:D003865), hypothalamic-pituitary-adrenal (HPA) axis abnormalities (MESH:D007027)
- **Chemicals:** Esketamine (MESH:C000629870)

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12579747/full.md

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Source: https://tomesphere.com/paper/PMC12579747