AI Article Synopsis

  • Immune checkpoint inhibitor (ICI) therapy is changing cancer treatment, making it more manageable like chronic diseases, but kidney transplant recipients (KTR) face unique risks with cancer due to their medication and health history.
  • Recent studies show that while KTR previously faced higher rejection risks (40%-50%), newer data indicates modified immunosuppression can lower this risk significantly (0%-12%).
  • There’s potential for using non-invasive biomarkers to assess risks and monitor for rejection in KTR undergoing ICI, though biopsies may still be needed for diagnosis, prompting a need for more research on safe and effective practices.

Article Abstract

Immune checkpoint inhibitor (ICI) therapy has enabled a paradigm shift in Oncology, with the treatment of metastatic cancer in certain tumor types becoming akin to the treatment of chronic disease. Kidney transplant recipients (KTR) are at increased risk of developing cancer compared to the general population. Historically, KTR were excluded from ICI clinical trials due to concern for allograft rejection and decreased anti-tumor efficacy. While early post-marketing data revealed an allograft rejection risk of 40%-50%, 2 recent small prospective trials have demonstrated lower rates of rejection of 0%-12%, suggesting that maintenance immunosuppression modification prior to ICI start modulates rejection risk. Moreover, objective response rates induced by ICI for the treatment of advanced or metastatic skin cancer, the most common malignancy in KTR, have been comparable to those achieved by immune intact patients. Non-invasive biomarkers may have a role in risk-stratifying patients before starting ICI, and monitoring for rejection, though allograft biopsy is required to confirm diagnosis. This clinically focused review summarizes current knowledge on complications of ICI use in KTR, including their mechanism, risk mitigation strategies, non-invasive biomarker use, approaches to treatment of rejection, and suggestions for future directions in research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11521864PMC
http://dx.doi.org/10.3389/ti.2024.13322DOI Listing

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