AI Article Synopsis

  • - Immune checkpoint inhibitors (ICIs) have shown promise in treating Lynch syndrome-associated colorectal and endometrial cancers, but their effectiveness combined with chemotherapy for Lynch syndrome-associated urothelial carcinoma (UC) is still uncertain.
  • - A specific case of a patient with recurrent and metastatic Lynch syndrome-associated UC demonstrated a sustained positive response to a combination of a PD-1 inhibitor and chemotherapy for over 31 months, with manageable side effects.
  • - The study suggests that the status of dMMR/MSI and PD-1 expression in UC could serve as useful indicators for predicting how well patients might respond to PD-1-targeted immunotherapy, warranting further investigation in clinical trials.

Article Abstract

Immune checkpoint inhibitors (ICIs) have shown encouraging outcomes against Lynch syndrome (LS)-associated colorectal cancer (CRC) and endometrial cancer with mismatch repair deficient/microsatellite instability-high (dMMR/MSI-H). However, there is as yet no clarity on the safety and efficacy of immunotherapy combined with chemotherapy in LS-associated urothelial carcinoma (UC). Here, we report a patient with recurrent and metastatic LS-associated UC who achieved sustained response to programmed death protein 1 (PD-1) inhibitor combined with chemotherapy over 31 months, during which the side effects of immunotherapy could be controlled and managed. Our findings indicate that the dMMR/MSI status and PD-1 expression in UC may have potential predictive value for the response to PD-1-targeted immunotherapy. Our case supports the inclusion of such combination and/or monotherapy for UC in clinical studies and using dMMR/MSI status and PD-1 expression as potential predictive biomarkers for assessment of the therapeutic response.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633672PMC
http://dx.doi.org/10.3389/pore.2022.1610638DOI Listing

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