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Renal Toxicities in Cancer Patients Receiving Immune-Checkpoint Inhibitors: A Meta-Analysis
Matteo Righini1,2, Veronica Mollica3,4, Alessandro Rizzo5
1Nephrology and Dialysis Unit, Santa Maria delle Croci Hospital, AUSL Romagna, 48121 Ravenna, Italy.
Abstract:
Aim: We performed a meta-analysis of the available clinical trials of immune-checkpoint inhibitors to assess risk differences and relative risks of renal toxicity. Methods: 17 randomized phase III studies were selected, including 10,252 patients. Results: The administration of immune-checkpoint inhibitors resulted in an overall low-grade, high-grade and all-grade renal toxicity Risk Difference of: 0.746% (95% CI 0.629% to 1.15%, p < 0.001—random), 0.61% (95% CI, 0.292−0.929%, p < 0.001—fixed) and 1.2% (95% CI, 0.601−1.85%—random), respectively. The pooled Relative Risk of low-grade, high-grade and all-grade renal toxicity was: 2.185 (95% CI 1.515−3.152—fixed), 2.610 (95% CI, 1.409−4.833, p = 0.002—fixed) and 2.473 (95% CI, 1.782−3.431, p < 0.001—fixed), respectively. An increased risk of renal toxicity was evident in some subgroups more than others. Conclusion: Immune-checkpoint inhibitors are associated with an increased risk of renal toxicity.
Insights
Immune-checkpoint inhibitors increase the risk of renal toxicity. This meta-analysis of 17 trials found a higher relative risk for all grades of kidney damage in patients receiving these treatments.
Area of Science:
- Oncology
- Nephrology
- Immunology
Background:
- Immune-checkpoint inhibitors (ICIs) are revolutionary cancer therapies.
- Assessing treatment-related adverse events, such as renal toxicity, is crucial for patient safety.
Purpose of the Study:
- To conduct a meta-analysis of clinical trials evaluating immune-checkpoint inhibitors.
- To quantify the risk differences and relative risks of renal toxicity associated with ICIs.
Main Methods:
- Systematic review and meta-analysis of 17 randomized phase III clinical trials.
- Inclusion of data from 10,252 patients treated with immune-checkpoint inhibitors.
Main Results:
- ICIs were associated with a statistically significant increased risk of all grades of renal toxicity (pooled Relative Risk = 2.473).
- Specific risk differences were calculated for low-grade (0.746%), high-grade (0.61%), and all-grade (1.2%) renal toxicity.
- Increased renal toxicity risk was observed in specific patient subgroups.
Conclusions:
- Immune-checkpoint inhibitors are linked to a notable increase in the risk of developing renal toxicity.
- Clinicians should carefully monitor patients receiving ICIs for potential kidney-related adverse events.
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