Multiple high-grade and rare immune-related adverse events in a colon cancer patient with genomic and cytokine profiling

Immunotherapy. 2022 Aug;14(11):843-850. doi: 10.2217/imt-2021-0298. Epub 2022 Jun 13.

Abstract

We report a case of multiple high-grade and rare immune-related adverse events (irAEs) in a patient with microsatellite instability-high (MSI-H) metastatic colorectal cancer (mCRC). A middle-aged MSI-H mCRC patient with metastases to the lungs and lymph nodes received several lines of chemotherapy and immunotherapy and developed five different high-grade irAEs during immunotherapy, including lymphadenitis, pneumonitis, hypophysitis, thyroiditis and transverse myelitis. Genomic profiling revealed high tumor mutational burden of 43 Muts/Mb. Cytokine profiling showed a threefold increase in MMP-9 shortly prior to the onset of lymphadenitis and a fourfold increase of Ang-1 1 week after the resolution of lymphadenitis. Further studies are warranted to investigate the association of MSI-H mCRC with irAEs and the role of cytokines in predicting irAEs.

Keywords: GITR; anti-PD-1; hypophysitis; immune checkpoint inhibitor; immune-related adverse events; lymphadenitis; pneumonitis; thyroiditis; transverse myelitis.

Plain language summary

Immune-related adverse events (irAEs) are a potential side effect of taking immunotherapy treatment for cancer. We report a case of a patient with a highly mutated form of metastatic colon cancer who developed five unique and severe irAEs while receiving immunotherapy. The patient developed inflammation of the lymph nodes, lungs, pituitary gland, thyroid and spinal cord. Genetic testing showed that the tumor was highly mutated (43 Muts/Mb). Analysis of cell signaling proteins called cytokines revealed that MMP-9 sharply increased before the onset of lymphadenitis and Ang-1 sharply increased after its resolution. Further research is needed to understand the relationship between highly mutated colon cancer and irAEs as well as the role of cytokines in predicting the onset and resolution of irAEs.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents, Immunological* / adverse effects
  • Colonic Neoplasms* / drug therapy
  • Cytokines
  • Genomics
  • Humans
  • Immune System Diseases*
  • Immunotherapy / adverse effects
  • Lymphadenitis* / chemically induced
  • Middle Aged
  • Programmed Cell Death 1 Receptor
  • Retrospective Studies

Substances

  • Antineoplastic Agents, Immunological
  • Cytokines
  • Programmed Cell Death 1 Receptor