Peripheral neuropathy and headache in cancer patients treated with immunotherapy and immuno-oncology combinations: the MOUSEION-02 study

Expert Opin Drug Metab Toxicol. 2021 Dec;17(12):1455-1466. doi: 10.1080/17425255.2021.2029405. Epub 2022 Jan 24.

Abstract

Introduction: Treatment-related neurotoxicity is a common side effect in cancer patients. However, few data are available regarding the risk of several neurotoxicities in patients treated with immune checkpoint inhibitors.

Areas covered: The MOUSEION-02 study is an up-to-date meta-analysis aimed at assessing the risk of peripheral neuropathy, peripheral sensory neuropathy, and headache in cancer patients receiving immunotherapy and immuno-oncology combinations. Patients receiving immunotherapy (as monotherapy or in combination with other anticancer agents) showed lower risk of all-grade peripheral neuropathy (RR, 0.50; 95% CI, 0.35-0.70) and all-grade peripheral sensory neuropathy (RR, 0.49; 95% CI, 0.30-0.79). Similarly, in patients treated with immune checkpoint inhibitor monotherapy, we observed lower risk of all-grade peripheral neuropathy (RR, 0.05; 95% CI, 0.03-0.10) and all-grade peripheral sensory neuropathy (RR, 0.11; 95% CI, 0.05-0.23). No differences were observed in terms of all-grade headache.

Expert opinion: Although the results of this meta-analysis should be interpreted with caution due to several issues, our study draws attention to immunotherapy-related neurotoxicity with the aim of maximizing clinical outcomes of cancer patients experiencing these not uncommon, and yet poorly studied, adverse events.

Keywords: Atezolizumab; avelumab; cancer; headache; immunotherapy; meta-analysis; nivolumab; pembrolizumab; peripheral neuropathy; peripheral sensory neuropathy.

Publication types

  • Meta-Analysis

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Headache / chemically induced
  • Headache / drug therapy
  • Humans
  • Immunotherapy / adverse effects
  • Neoplasms* / drug therapy
  • Peripheral Nervous System Diseases* / chemically induced

Substances

  • Antineoplastic Agents