Brief Communication PD1-related Nephrotoxicity: Optimizing Its Clinical Management Through Histopathologic Features
Anna M Di Giacomo1,2, Andrea Guarnieri3, Sergio A Tripodi4
1Center for Immuno-Oncology, University Hospital.
Journal of Immunotherapy (Hagerstown, Md. : 1997)
|February 8, 2022
Summary
Immune-related nephrotoxicity from immune-checkpoint inhibitors is rare but serious. Treating it like kidney transplant rejection rapidly improved kidney function in a small patient group.
Area of Science:
- Nephrology
- Immunology
- Oncology
Background:
- Immune-related nephrotoxicity (ir-N) is a rare adverse event associated with immune-checkpoint inhibitor (ICI) therapy.
- The clinical management of ir-N remains a subject of ongoing debate and research.
Purpose of the Study:
- To investigate the histological features of ir-N in patients treated with ICI.
- To evaluate the efficacy of a treatment strategy adapted from kidney transplant rejection protocols for managing ir-N.
Main Methods:
- Retrospective analysis of 501 patients treated with ICI.
- Kidney biopsy performed on 6 patients presenting with clinical signs of acute kidney injury due to ir-N.
- Histopathological examination of kidney biopsies.
- Implementation of acute allograft kidney rejection management protocols.
Main Results:
- Histology revealed acute tubule-interstitial nephritis in all biopsied patients, mimicking acute T-cell-mediated kidney transplant rejection.
- Patients treated with the adapted protocol showed rapid improvement in renal function.
Conclusions:
- Histological findings of immune-mediated acute kidney injury in ICI-treated patients can guide clinical management.
- Adapting strategies used for kidney transplant rejection may be an effective approach for managing ir-N.
- Further research is warranted to optimize ir-N management strategies.
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