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Updated: Nov 4, 2025

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Adjuvant Tyrosine Kinase Inhibitors in Renal Cell Carcinoma: A Concluded Living Systematic Review and Meta-Analysis
Irbaz Bin Riaz1, Rabbia Siddiqi2, Mahnoor Islam2
1Mayo Clinic, Phoenix, AZ.
Purpose:
Multiple large clinical trials have investigated adjuvant tyrosine kinase inhibitors (TKIs) to reduce the risk of cancer recurrence and progression to metastasis in high-risk renal cell carcinoma. We sought to maintain living and interactive evidence on this topic, until a high level of certainty is reached for key clinical outcomes such that further updates become unnecessary and unlikely to change clinical practice.
Methods:
We created a living interactive evidence synthesis platform to maintain a continuously updated meta-analysis on TKI monotherapy in adjuvant renal cell carcinoma. We implemented an automated search strategy with weekly updates to identify randomized phase 2 and 3 clinical trials. Study selection, appraisal, and data extraction were done in duplicate. Cumulative meta-analysis was performed using Analyzer Module in Living Interactive Evidence platform. For each outcome (overall survival [OS], disease-free survival [DFS], and all-cause and treatment-related adverse events), we assessed certainty of evidence using GRADE approach and conducted trial sequential analysis.
Results:
This final update includes five randomized trials including recently updated data from PROTECT trial. Meta-analysis shows that adjuvant TKI monotherapy offers no benefit in OS (hazard ratio, 1.01; 95% CI, 0.91 to 1.12, high certainty) or DFS (hazard ratio, 0.92; 95% CI, 0.86 to 1.00, high certainty) and significantly increases adverse event risk. Lack of benefit was consistent across subgroups including highest-risk patients (test for subgroup differences: P = .32). Optimal information size criteria were met, and there was high certainty of evidence for lack of DFS and OS benefit for adjuvant TKIs.
Conclusion:
There is no guidance on when to stop maintaining a living review. In this example, we used trial sequential analysis and high certainty of evidence (future clinical trials unlikely to change current conclusions) as a benchmark to conclude a living review in view of convincing evidence.
Insights
Adjuvant tyrosine kinase inhibitors (TKIs) do not improve survival in high-risk kidney cancer patients. This living review found no benefit for overall survival or disease-free survival, with increased adverse events.
Area of Science:
- Nephrology
- Oncology
- Clinical Trials
Background:
- Adjuvant tyrosine kinase inhibitors (TKIs) are investigated for high-risk renal cell carcinoma (RCC) to prevent recurrence and metastasis.
- Living evidence synthesis aims to provide continuously updated meta-analyses until clinical certainty is achieved.
Purpose of the Study:
- To maintain a living, interactive meta-analysis of adjuvant TKI monotherapy in RCC.
- To assess clinical outcomes including overall survival (OS), disease-free survival (DFS), and adverse events.
- To determine when sufficient evidence warrants concluding the living review.
Main Methods:
- A living interactive evidence synthesis platform with automated weekly searches for randomized phase 2 and 3 trials.
- Duplicate study selection, appraisal, and data extraction.
- Cumulative meta-analysis, GRADE certainty assessment, and trial sequential analysis (TSA).
Main Results:
- Analysis of five randomized trials, including updated PROTECT data, shows no OS or DFS benefit from adjuvant TKIs.
- Hazard ratios: OS 1.01 (95% CI, 0.91-1.12) and DFS 0.92 (95% CI, 0.86-1.00), both with high certainty.
- TKIs significantly increased adverse events; lack of benefit was consistent across subgroups, meeting TSA optimal information size criteria.
Conclusions:
- Adjuvant TKI monotherapy provides no survival benefit in high-risk RCC and increases risks.
- High certainty of evidence and TSA indicate that further trials are unlikely to alter these conclusions.
- The living review was concluded based on convincing evidence and established benchmarks.
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