Impact of tumor immunotherapy on kidney injury and multi-organ outcomes: a mechanistic and clinical perspective - Summary - MDSpire

Impact of tumor immunotherapy on kidney injury and multi-organ outcomes: a mechanistic and clinical perspective

  • By

  • Lan Jiang

  • Jing Wang

  • Shihong Xiong

  • Sumei Min

  • Na Gong

  • July 10, 2026

  • 0 min

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Objective:

To systematically evaluate ICI efficacy and safety profiles concerning renal and multi-organ outcomes in cancer patients, focusing on underlying mechanisms and protective interventional approaches.

Approach:
  • Literature Search: Comprehensive systematic literature search across multiple databases (PubMed, Cochrane Library, Embase, Web of Science, Scopus) from January 2000 to December 2025.
  • Narrative Synthesis: Integration of evidence from diverse study designs to generate mechanistic hypotheses and clinical insights, rather than estimating pooled effect sizes.
  • Quality Appraisal: Structured study selection and quality appraisal using established tools (Cochrane RoB 2.0, ROBINS-I, GRADE) to enhance transparency and evaluate evidence certainty.
Key Findings:
  • ICIs are associated with acute kidney injury, particularly acute tubulointerstitial nephritis.
  • Multi-organ immune-related adverse events (irAEs) include myocarditis.
  • Mechanistic investigations highlight PD-1/PD-L1 pathway disruption, metabolic dysregulation, and immune cell heterogeneity as central pathways.
  • Quantitative effect estimates showed significant interstudy variability.
Interpretation:

Tumor immunotherapy significantly impacts renal and multi-organ homeostasis, with moderate-certainty evidence supporting the need for immune microenvironment-targeted protective strategies.

Limitations:
  • Methodological heterogeneity precluded formal meta-analysis.
  • Existing literature predominantly focuses on isolated organ systems, lacking a holistic perspective.
  • Variable efficacy of glucocorticoids remains unexplained at a molecular level.
Conclusion:

Future investigations should prioritize biomarker-guided precision approaches to balance efficacy and safety considerations, with a focus on tissue-specific immune microenvironment interactions.

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