AI Article Synopsis

  • The aging population and improved survival rates after kidney transplants are leading to more cases of cancer before and after these surgeries, prompting a need for better screening and treatment strategies.
  • Kidney transplant recipients face a higher risk for cancer, yet current guidelines for screening and treatment mainly draw from data on the general public, which may not be fully applicable to them.
  • Effective management of cancer in kidney transplant patients involves balancing cancer treatment with immunosuppression to prevent graft rejection, requiring personalized assessments of risks and benefits due to the rise of new cancer therapies.

Article Abstract

As the population ages and post-transplant survival improves, pretransplant and post-transplant malignancy are becoming increasingly common. In addition, rapid advances in cancer therapies and improving outcomes prompt us to rethink pretransplant cancer-free wait time and screening strategies. Although kidney transplant recipients (KTRs) are at higher risk of developing cancer, epidemiological data on how to best screen and treat cancers in KTRs are incomplete. Thus, current recommendations are still largely on the basis of studies in the general population, and their validity in KTRs is uncertain. Kidney transplant candidates without prior cancer should be evaluated for latent malignancies even in the absence of symptoms. Conversely, individuals with a history of malignancy require thorough monitoring to detect potential recurrences or de novo malignancies. When treating KTRs with cancer, reducing immunosuppression can enhance antitumor immunity, yet this also increases the risk of graft rejection. Optimal treatment and immunosuppression management remains undefined. As the emergence of novel cancer therapies adds complexity to this challenge, individualized risk-benefit assessment is crucial. In this review, we discuss up-to-date data on pretransplant screening and cancer-free wait time, as well as post-transplant cancer screening, prevention strategies, and treatment, including novel therapies such as immune checkpoint inhibitors and chimeric antigen receptor T-cell therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556922PMC
http://dx.doi.org/10.34067/KID.0000000000000545DOI Listing

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