Memantine efficacy in chemotherapy-induced peripheral neuropathy: double-blind placebo-controlled randomised clinical trial
Clinical Snapshot
PICO Framework
| P — Population | 176 adults with chemotherapy-induced peripheral neuropathy (CIPN) |
| I — Intervention | Memantine 5mg daily for 3 days, then titrated to 20mg daily over 8 weeks |
| C — Comparator | Matched placebo tablets for 8 weeks |
| O — Outcomes | Neuropathic pain severity (McGill Pain Questionnaire) and neuropathy improvement (tuning fork test) |
Bottom Line
This Iranian RCT suggests memantine may reduce chemotherapy-induced peripheral neuropathy symptoms compared to placebo over 8 weeks. While the double-blind design and statistical significance are encouraging, the abstract lacks crucial methodological details including randomisation methods, baseline characteristics, dropout rates, and safety data. The clinical significance appears promising with patients achieving minimal clinically important differences, but confidence intervals and effect sizes are not reported. Given memantine's established safety profile in other conditions and the limited effective treatments for CIPN, this warrants further investigation. However, clinicians should await full publication details before considering off-label use, particularly regarding adverse effects and patient selection criteria. The intervention appears feasible in Australian practice but would require specialist oversight given the off-label indication.
Key Findings
P Value: p<0.001 for both outcome measures
Effect Size: Not reported in abstract
Primary Outcome: Significant improvement in neuropathy (tuning fork test) and pain scores (McGill Pain Questionnaire)
Nnt Or Sensitivity: Not calculable from available data
Confidence Interval: Not reported
Clinical Application
Memantine is orally administered, well-tolerated, and requires standard titration protocol Memantine is PBS-listed for dementia; off-label use for CIPN would require specialist consideration and patient consent Adult cancer patients with established CIPN from various chemotherapeutic agents
Abstract
BACKGROUND AND AIMS: Chemotherapy-induced peripheral neuropathy (CIPN) is a detrimental side effect of chemotherapeutic agents. If left untreated, CIPN can persist for several years following the chemotherapy. CIPN management may enhance the quality of life of the affected patients. This study evaluated the efficacy of memantine, an antagonist of N-methyl-D-aspartate, in CIPN management. METHODS: This double-blinded randomised clinical trial was performed on 176 individuals with CIPN. Patients were randomised to either the memantine or placebo groups (88 in each). The memantine group received a single daily dose of 5 mg for the initial 3 days. Subsequently, the dosage was increased to 20 mg per day, with 5 mg increments every 3 days. The placebo group received tablets of equal shape and size. All individuals received medications for 8 weeks. The McGill pain questionnaire and tuning fork test were used to evaluate the severity of neuropathic pain in patients, both at baseline and after the intervention ended. RESULTS: Based on tuning fork test results, significant improvement in neuropathy was observed among patients who received memantine compared with those who received placebo (p<0.001 vs 0.665). McGill pain questionnaire score revealed a significant difference between memantine and placebo groups (p<0.001 for both groups). This difference was also significant after performing intention-to-treat analysis. Moreover, a higher proportion of patients in the memantine group achieved minimal clinically important difference. CONCLUSION: The use of memantine mitigated the CIPN intensity. Thus, it appears that memantine is a promising option for the management of patients experiencing CIPN.
References
- 1.Esmaili, N., Beheshtirouy, S., Sanaat, Z., Shaseb, E., Sarbakhsh, P., & Ghaffary, S. (2024). Memantine efficacy in chemotherapy-induced peripheral neuropathy: double-blind placebo-controlled randomised clinical trial. BMJ Supportive & Palliative Care. https://doi.org/10.1136/spcare-2024-005348
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