Risk of toxicity with immunotherapy-tyrosine kinase inhibitors for metastatic renal cell carcinoma: a meta-analysis of randomized controlled trials.
Alessandro RizzoVeronica MollicaMatteo SantoniMatteo RoselliniAndrea MarchettiFrancesco MassariPublished in: Future oncology (London, England) (2021)
Aim: Few data are available regarding the safety profile of immunotherapy-tyrosine kinase inhibitor (IO-TKI) combinations in metastatic renal cell carcinoma. The authors investigated all-grade and grade 3-4 (G3-4) adverse events in trials comparing IO-TKI combinations with sunitinib monotherapy. Methods: The relative risks of several all-grade and G3-4 adverse events were analyzed. Results: Relative risks were similar between patients receiving IO-TKI combinations versus sunitinib monotherapy. However, the use of IO-TKI combinations was associated with a higher risk of all-grade and G3-4 diarrhea, all-grade hypothyroidism, G3-4 decreased appetite, all-grade and G3-4 aspartate transaminase increase and all-grade and G3-4 alanine transaminase increase. Conclusion: The results of the authors' meta-analysis suggest that risks of treatment-related adverse events should be carefully considered when choosing IO-TKI combinations in metastatic renal cell carcinoma patients.
Keyphrases
- metastatic renal cell carcinoma
- tyrosine kinase
- systematic review
- chronic myeloid leukemia
- advanced non small cell lung cancer
- end stage renal disease
- combination therapy
- newly diagnosed
- chronic kidney disease
- oxidative stress
- randomized controlled trial
- ejection fraction
- open label
- clinical trial
- prognostic factors
- peritoneal dialysis
- replacement therapy
- atomic force microscopy
- study protocol
- high speed