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Updated: Sep 16, 2025

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Successful Management of Immune-Mediated Myelitis in a Renal Cancer Patient: A Case Report
Paula Rodríguez Payá1,2, Álvaro Muñoz Abad1,2, Beatriz Grau Mirete1,2
1Department of Medical Oncology, Hospital General Universitario de Elche, Elche, Spain.
Introduction:
Immune checkpoint inhibitors (ICIs) have revolutionized metastatic renal cell carcinoma treatment, significantly improving survival outcomes. However, ICIs are linked to immune-related adverse events (irAEs), which can impact multiple organs. Neurological irAEs, such as myelitis, are rare but potentially severe.
Case Presentation:
We describe a 54-year-old male with high-grade clear cell renal carcinoma treated with nivolumab and ipilimumab. After four cycles, he developed hypophysitis, adrenal insufficiency, and hypothyroidism, managed with hydrocortisone and levothyroxine, while continuing nivolumab monotherapy. In August 2022, he experienced right eyelid ptosis and right hand weakness. Cranial magnetic resonance imaging (MRI) showed improvement in the sellar lesion, and chronic sensorimotor polyneuropathy was diagnosed, ruling out myasthenia gravis. Nivolumab treatment continued. By December 2022, after seven cycles, the patient developed back pain and dysesthesias, with MRI confirming transverse myelitis from C7 to T3. Nivolumab was discontinued, and high-dose corticosteroids (1 g methylprednisolone daily for 5 days) led to clinical improvement. A 12-week taper followed, with no symptom recurrence. Disease progression in April 2023 led to a switch to pazopanib, maintaining a partial response for 6 months.
Conclusion:
This case emphasizes the serious nature of neurological irAEs from ICIs and the critical need for early detection and management. It also highlights the increased risk of subsequent irAEs after an initial event, underscoring the importance of vigilant monitoring.
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