The Emerging Role of Ketamine and Esketamine in the Concurrent Management of Pain and Depression in Cancer Patients: Evidence and Implications for Practice

Journal of Pain & Palliative Care Pharmacotherapy  – December 27, 2025

Source: OpenAlex

Summary

Ketamine and its S-enantiomer esketamine show promise for alleviating both pain and depression in cancer patients. Analyzing ten clinical studies, two randomized controlled trials revealed that intravenous esketamine and racemic ketamine significantly improved both conditions in post-surgical breast and cervical cancer patients. Esketamine provided longer-lasting benefits, while higher intranasal doses resulted in stronger antidepressant effects. Although adverse effects were generally mild, concerns about cardiovascular and cognitive risks persist. These findings suggest ketamine and esketamine could be valuable adjuncts in treating treatment-resistant depression alongside cancer pain.

Abstract

Cancer patients frequently experience pain and depression, yet current guidelines address these conditions separately and do not recommend a single agent for concurrent management. Ketamine and its S-enantiomer esketamine, through N-methyl-D-aspartate receptor antagonism and glutamate modulation, may offer dual benefit. This paper examined ten clinical studies published between 2018 and 2024 evaluating ketamine and esketamine for concurrent cancer-related pain and depression. Evidence was heterogeneous but promising. Two randomized controlled trials in post-surgical breast and cervical cancer patients demonstrated that intravenous (IV) esketamine and racemic ketamine improved both pain and depression, with esketamine showing greater, longer-lasting benefit. When pain was the primary outcome, results were mixed: IV esketamine provided dual benefit in one trial, whereas racemic ketamine produced variable or nonsignificant effects across IV, intranasal (IN), and oral routes. In depression-focused studies, IV and IN administration consistently improved mood, even without pain relief. Dose-response relationships were observed, with esketamine outperforming ketamine and higher IN dosing yielding stronger antidepressant effects. Adverse effects were generally mild and transient, though cardiovascular, urinary, and cognitive risks remain concerns. With rapid dual action, ketamine and esketamine may serve as valuable adjunctive therapies in palliative care. Further studies should clarify optimal dosing, route, and long-term safety.

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