Journal
NEUROLOGICAL SCIENCES
Volume 42, Issue 4, Pages 1405-1409Publisher
SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-020-04604-1
Keywords
Targeted therapies; Immune-related adverse events; BRAF and MEK inhibitors; Imatinib; Neuromuscular complications; Myasthenia gravis
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Funding
- Universita degli Studi di Genova within the CRUI-CARE Agreement
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Through the description of two cases, we emphasize the importance of neuromuscular complications, which may occur long after treatment initiation or in patients receiving not only the newest ICPi, but also older and seemingly more familiar targeted therapies. Even in the latter cases, an immune-mediated off-target pathogenic mechanism can be hypothesized, with potentially life-threatening consequences if not promptly diagnosed and managed appropriately.
Introduction In the last years, many new drugs have been developed targeting different oncology pathways, overall improving both quality of life and survival in several malignancies. However, the increase of those therapies is associated with novel toxicities, mainly immune-related adverse events (irAEs), never observed before. Different irAEs are now well characterized, and, among them, neuromuscular complications, following immune checkpoint inhibitor (ICPi) therapy, are increasingly studied and described. However, there are also neurological complications related to the use of other targeted therapies, less known and probably underestimated. Herein we describe two oncological patients who developed neuromuscular diseases after administration of targeted therapies, different from ICPi. Case reports The first patient was treated with the combination of Vemurafenib and Cobimetinib, BRAF and MEK inhibitors, respectively, for a cutaneous melanoma. One year after the beginning of the combined treatment, she developed a sub-acute motor neuropathy with predominant cranial nerve involvement. She was successfully treated with methylprednisolone. The second patient received therapy with Imatinib, tyrosine kinase inhibitor and precursor of the targeted therapy, for a gastrointestinal stromal tumour. Few days after the first administration, he developed generalized myasthenia gravis with respiratory failure. Clinical remission was obtained with plasma-exchange, intravenous immunoglobulins and steroids. Discussion and Conclusion We strengthen the relevance of neuromuscular complications which may occur long after treatment start or in patients receiving not only the latest ICPi but also older and apparently better-known targeted therapies. Also in the latter cases, an immune-mediated off-target pathogenic mechanism can be hypothesized, and consequences can be life threatening, if not promptly diagnosed and appropriately managed.
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