# Urgent considerations on renal immune-related adverse events in oncology practice

**Authors:** Wen-Qing Lv, Jing-Yao Lu, Jun Li, Dao-Yuan Lv, Qi Ke

PMC · DOI: 10.3389/fimmu.2025.1714090 · Frontiers in Immunology · 2026-02-10

## TL;DR

This paper reviews how immune therapy can cause kidney problems in cancer patients and highlights important considerations for managing these issues.

## Contribution

The paper systematically examines the causes, biomarkers, and management of kidney-related immune side effects in cancer patients.

## Key findings

- Renal irAEs often require treatment discontinuation and can worsen cancer outcomes.
- Genetic susceptibility and non-invasive biomarkers are important for managing renal irAEs.
- Targeted immunotherapy may improve both kidney health and cancer survival.

## Abstract

In recent years, immune checkpoint inhibitors (ICIs) have emerged as a critical component of hematological malignancies and solid malignant tumors therapy. However, clinical practice has revealed that these agents may induce immune-related adverse events (irAEs). Notably, renal irAEs stands out as a significant clinical concern, frequently necessitating treatment discontinuation and thereby enabling tumor progression. Renal irAEs constitutes a critical consideration for patients with cancer complicated by chronic kidney disease (CKD). This review systematically examines the immunologic pathogenesis of ICIs-induced renal disease, susceptibility genes, non-invasive biomarkers, and efficient intervention strategies. It further analyzes the critical considerations regarding renal irAEs that oncologists must address, based on real-world evidence from ICIs therapy in cancer patients with CKD, including those who are renal transplantation recipients or have end-stage renal disease (ESRD). Additionally, the promising targeted immunotherapy for malignant tumors is expected to improve both renal outcomes and survival prognosis in cancer patients.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), end-stage renal disease (MONDO:0004375)

## Full-text entities

- **Genes:** FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}, SLA-5 (MHC class I antigen 5) [NCBI Gene 100135029] {aka PG3I, SLA-1, SLA-5b}, CXCL11 (C-X-C motif chemokine ligand 11) [NCBI Gene 6373] {aka H174, I-TAC, IP-9, IP9, SCYB11, SCYB9B}, TRBV25-1 (T cell receptor beta variable 25-1) [NCBI Gene 28562] {aka TCRBV11S1A1T, TCRBV25S1, TRBV251}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, ERVK-3 (endogenous retrovirus group K member 3) [NCBI Gene 100862689] {aka c3_B}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 100126861] {aka Akt, PKB}, CD28 [NCBI Gene 100738615], CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CD80 (CD80 molecule) [NCBI Gene 397161] {aka B7-1}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, APC (APC regulator of WNT signaling pathway) [NCBI Gene 100517932] {aka APC1}, CD274 (CD274 molecule) [NCBI Gene 574058] {aka PDL1}, CXCL9 (C-X-C motif chemokine ligand 9) [NCBI Gene 4283] {aka CMK, Humig, MIG, SCYB9, crg-10}, PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 574057] {aka PDL2}, GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}, SHP [NCBI Gene 100127458], CD86 (CD86 molecule) [NCBI Gene 397441], PDCD1 (programmed cell death 1) [NCBI Gene 100533201], REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, CCL26 (C-C motif chemokine ligand 26) [NCBI Gene 10344] {aka IMAC, MIP-4a, MIP-4alpha, SCYA26, TSC-1}, PCCA (propionyl-CoA carboxylase subunit alpha) [NCBI Gene 5095], CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, RPS26 (ribosomal protein S26) [NCBI Gene 6231] {aka DBA10, S26, eS26}, CD163 (CD163 molecule) [NCBI Gene 9332] {aka M130, MM130, SCARI1}, IL21 (interleukin 21) [NCBI Gene 59067] {aka CVID11, IL-21, Za11}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, MMP12 (matrix metallopeptidase 12) [NCBI Gene 4321] {aka HME, ME, MME, MMP-12}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, SYK (spleen associated tyrosine kinase) [NCBI Gene 6850] {aka IMD82, p72-Syk}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, JUN (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3725] {aka AP-1, AP1, c-Jun, cJUN, p39}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 397286], IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, MS4A2 (membrane spanning 4-domains A2) [NCBI Gene 2206] {aka APY, ATOPY, FCER1B, FCERI, IGEL, IGER}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, ADAD1 (adenosine deaminase domain containing 1) [NCBI Gene 132612] {aka Tenr}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, NT5E (5'-nucleotidase ecto) [NCBI Gene 4907] {aka CALJA, CD73, E5NT, NT, NT5, NTE}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 100127359] {aka FRAP1}, CD27 (CD27 molecule) [NCBI Gene 939] {aka S152, S152. LPFS2, T14, TNFRSF7, Tp55}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, RBP4 (retinol binding protein 4) [NCBI Gene 5950] {aka MCOPCB10, RDCCAS}, IFI27 (interferon alpha inducible protein 27) [NCBI Gene 3429] {aka FAM14D, ISG12, ISG12A, P27}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL2 (Interleukin 2 level) [NCBI Gene 101055066]
- **Diseases:** minimal change (MESH:D009402), C3 nephropathy (MESH:C565169), urinary irritation (MESH:D001523), graft failure (MESH:D051437), cystitis (MESH:D003556), uremic (MESH:D006463), ATN (MESH:D007683), oliguria (MESH:D009846), myeloma (MESH:D009101), Renal irAEs (MESH:D002318), lung cancer (MESH:D008175), renal (MESH:D006030), hepatocellular carcinoma (MESH:D006528), infection (MESH:D007239), fever (MESH:D005334), ESRD (MESH:D007676), impaired immune function (MESH:D007154), ANCA (MESH:D056648), hematological malignancies (MESH:D019337), diabetes mellitus (MESH:D003920), sarcoidosis (MESH:D012507), MPGN (MESH:D015432), thrombocytopenia (MESH:D013921), autoimmune lupus nephritis (MESH:D008181), endocrine injury (MESH:D004700), Tumor (MESH:D009369), proteinuria (MESH:D011507), kidney cancer (MESH:D007680), steroid (MESH:D016114), IgA nephropathy (MESH:D005922), tubular impairment (MESH:D000230), pyuria (MESH:D011776), head and neck squamous cell carcinoma (MESH:D000077195), disorders of the complement system (MESH:D009422), Kaposi sarcoma (MESH:D012514), urinary system injury (MESH:D057772), ureteral and cystitis (MESH:D014515), renal tubular acidosis (MESH:D000141), urinary tract infections or obstructions (MESH:D014552), renal cell carcinoma (MESH:D002292), lupus (MESH:D008180), toxicity (MESH:D064420), non-small cell lung cancer (MESH:D002289), CKD (MESH:D051436), edema (MESH:D004487), hypovolemia (MESH:D020896), hydronephrosis (MESH:D006869), renal involvement (MESH:C565423), infectious (MESH:D003141), lip cancer (MESH:D008048), immune complex glomerular lesions (MESH:D007105), anti-glomerular basement membrane disease (MESH:D019867), metabolic acidosis (MESH:D000138), eosinophilia (MESH:D004802), rash (MESH:D005076), glomerulonephropathy (MESH:D015433), Vasculitis (MESH:D014657), interstitial nephritis (MESH:D009395), anemia (MESH:D000740), AIN (MESH:C564356)
- **Chemicals:** dexamethasone (MESH:D003907), nivolumab (MESH:D000077594), ipilimumab (MESH:D000074324), calcium phosphate (MESH:C020243), TI (MESH:D014025), Cu (MESH:D003300), pembrolizumab (MESH:C582435), Cr (MESH:D002857), Rituximab (MESH:D000069283), DMXAA (MESH:C066668), creatinine (MESH:D003404), FDG (MESH:D019788), APCP (MESH:C083343), azathioprine (MESH:D001379), aldosterone (MESH:D000450), Infliximab (MESH:D000069285), Tofacitinib (MESH:C479163), cyclophosphamide (MESH:D003520), Sb (MESH:D000965), metal (MESH:D008670), BioRender (-), MMF (MESH:D009173), fluindione (MESH:C017673), Steroid (MESH:D013256), Prednisone (MESH:D011241), cyclosporine (MESH:D016572), galunisertib (MESH:C557799), tocilizumab (MESH:C502936)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Saccharomyces boulardii [taxon 252598], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Homo sapiens (human, species) [taxon 9606], Glycyrrhiza uralensis (Chinese licorice, species) [taxon 74613]
- **Mutations:** rs16957301, rs3810610, rs17388568

## Full text

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## References

141 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929483/full.md

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Source: https://tomesphere.com/paper/PMC12929483