Alkylating Agent-Induced High Tumor Mutational Burden in Medullary Thyroid Cancer and Response to Immune Checkpoint Inhibitors: Two Case Reports

Thyroid. 2023 Nov;33(11):1368-1373. doi: 10.1089/thy.2023.0144. Epub 2023 Oct 9.

Abstract

Background: Patients with metastatic medullary thyroid cancer (MTC) who progressed under tyrosine kinase inhibitors can benefit from an alkylating agent such as dacarbazine or temozolomide. Patient Findings: We describe two patients with metastatic MTC who developed a hypermutant phenotype after alkylating agent treatment. This phenotype was characterized by a high tumor mutational burden (TMB) and a mutational signature indicative of alkylating agent mutagenesis (single-base substitution 11). Both patients received immune checkpoint inhibitors, with partial morphological responses, clinical benefit, and progression-free survival of 6 and 9 months, respectively. Summary and Conclusions: Based on the described observations, we suggest that a hypermutant phenotype may be induced after alkylating agent treatment for MTC and the sequential use of immunotherapy should be further explored as a treatment option for MTC patients with increased TMB.

Keywords: alkylating agents; hypermutant phenotype; immune checkpoint inhibitors; medullary; mutational signature; thyroid cancer.

Publication types

  • Case Reports

MeSH terms

  • Alkylating Agents / adverse effects
  • Carcinoma, Neuroendocrine* / drug therapy
  • Carcinoma, Neuroendocrine* / genetics
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Thyroid Neoplasms* / drug therapy
  • Thyroid Neoplasms* / genetics

Substances

  • Alkylating Agents
  • Immune Checkpoint Inhibitors

Supplementary concepts

  • Thyroid cancer, medullary