AI Article Synopsis

  • Immune checkpoint inhibitors (ICIs) are a promising cancer treatment that can have serious side effects, especially in patients with preexisting autoimmune disorders like multiple sclerosis (MS).
  • A case study reported significant improvement in a man with both metastatic non-small cell lung cancer (NSCLC) and MS after treatment with atezolizumab, but he also experienced a severe MS flare that stopped further treatment.
  • Diagnosing complications in patients with both MS and brain tumors is complicated because symptoms could indicate tumor growth, an MS flare-up, or radiation necrosis, making management difficult.

Article Abstract

Background: Immune checkpoint inhibitors (ICIs) have become an increasingly important tool in cancer treatment, revealing durable responses in several different types of tumors, including NSCLCs. Nevertheless, ICIs carry a risk of immune-mediated toxicities. There is a paucity of data for concurrent use of these agents in patients with autoimmune disorders, such as multiple sclerosis (MS).

Case Presentation: We report a case of a man with a history of MS and metastatic NSCLC with brain metastases who had cancer progression after receiving chemotherapy, whole-brain radiation therapy, and stereotactic radiosurgery to brain lesions and was treated with the programmed death-ligand 1 inhibitor, atezolizumab. He had dramatic clinical and radiographic benefit but developed a severe MS flare and neurologic decline precluding further treatment. Considerable growth of a previously radiated brain lesion prompted resection, with pathologic findings consistent with radiation necrosis and demyelination without viable tumor cells.

Conclusions: Although patients with preexisting autoimmune diseases, including MS, might be at an increased risk of developing immune-related adverse events with ICIs, they may also experience anticancer benefit. Intracranial disease can be challenging to accurately diagnose in a patient with MS who previously underwent radiation, as progressing lesions can be tumor growth, MS flare, or radiation necrosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474265PMC
http://dx.doi.org/10.1016/j.jtocrr.2021.100183DOI Listing

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