AI Article Synopsis

  • A 70-year-old man with extensive-stage small-cell lung cancer developed Lambert-Eaton myasthenic syndrome (LEMS) after starting maintenance immunotherapy with atezolizumab following chemotherapy.
  • He experienced muscle weakness and fatigue, leading to a diagnosis of LEMS as an immune-related adverse event due to the immunotherapy.
  • After stopping atezolizumab and receiving treatment with steroids and immunoglobulin, his symptoms improved, and there has been no recurrence of neurological issues or progression of his cancer for 18 months.

Article Abstract

The case of a 70-year-old man who developed Lambert-Eaton myasthenic syndrome (LEMS) while receiving  treatment for extensive-stage small-cell lung cancer (SCLC) is presented. He started receiving maintenance immunotherapy with atezolizumab following four cycles of combination therapy with , carboplatin, and etoposide. After five cycles of maintenance  therapy, he complained of muscle weakness in the lower limbs and fatigue. Electromyographic findings and positive results for anti-P/Q-type voltage-gated calcium channel antibody made a diagnosis of LEMS. Based on the onset time of LEMS and the state of his underlying cancer at the time of the appearance of neurological symptoms, he was diagnosed with LEMS as an immune-related adverse event (irAE) induced by atezolizumab. After discontinuing atezolizumab treatment and initiating combination therapy with steroid pulse plus intravenous immunoglobulin, his neurological symptoms improved. Although 18 months have passed since the discontinuation of atezolizumab treatment, there has been neither recurrence of neurological symptoms nor a progression of his cancer without salvage chemotherapy. This is a rare case of LEMS as a neurological irAE induced by atezolizumab. Clinicians must be aware of the potential for LEMS to develop in SCLC patients taking atezolizumab treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908354PMC
http://dx.doi.org/10.7759/cureus.33557DOI Listing

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