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Updated: Feb 17, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Examining the bleeding incidences associated with targeted therapies used in metastatic renal cell carcinoma
MacKenzie Crist1, Elizabeth Hansen2, Lipika Chablani1
1Wegmans School of Pharmacy, St. John Fisher College, Rochester, NY, United States.
Abstract:
A systematic review was conducted to illustrate the bleeding risks associated with targeted therapies used in the treatment of metastatic renal cell carcinoma (mRCC). Eligible studies included phase II, III, or IV clinical trials using pazopanib, sunitinib, cabozantinib, lenvatinib, everolimus, temsirolimus, bevacizumab, axitinib, and/or sorafenib in the setting of mRCC. Types of bleeding event(s), bleeding event frequency, and incidence of thrombocytopenia were collected from the relevant articles. ClinicalTrials.gov was also searched for incidence of "Serious bleeding adverse effects" reported in these trials. The incidences of bleeding events ranged from 1 to 36%, and incidences of thrombocytopenia ranged from 2 to 78%. Available serious bleeding adverse events ranged from 1 to 7%. The highest percentage of bleeding incidences were seen with bevacizumab, while the lowest percentage of bleeding incidences were seen with axitinib. All of the included trials were of high quality per Jadad scoring.
Insights
This review highlights bleeding risks in metastatic renal cell carcinoma (mRCC) targeted therapies. Bevacizumab showed the highest bleeding incidence, while axitinib had the lowest among these cancer treatments.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Metastatic renal cell carcinoma (mRCC) is a complex cancer requiring targeted therapies.
- Understanding the adverse event profiles of these treatments is crucial for patient management.
- Bleeding events and thrombocytopenia are known potential side effects of several mRCC drugs.
Purpose of the Study:
- To systematically review and illustrate the bleeding risks associated with targeted therapies used in mRCC treatment.
- To compare the incidence of bleeding events and thrombocytopenia across different targeted agents.
- To identify specific drugs with higher or lower bleeding risk profiles.
Main Methods:
- A systematic review of phase II, III, or IV clinical trials involving specific mRCC targeted therapies.
- Data collection included types of bleeding events, frequency, and incidence of thrombocytopenia.
- Searched ClinicalTrials.gov for serious bleeding adverse effects.
- Assessed trial quality using Jadad scoring.
Main Results:
- Bleeding event incidences ranged from 1% to 36%.
- Thrombocytopenia incidences ranged from 2% to 78%.
- Serious bleeding adverse events ranged from 1% to 7%.
- Bevacizumab exhibited the highest bleeding incidence, whereas axitinib demonstrated the lowest.
Conclusions:
- Targeted therapies for mRCC are associated with a spectrum of bleeding risks and thrombocytopenia.
- Bevacizumab is linked to a higher incidence of bleeding events compared to other agents reviewed.
- Axitinib appears to have a comparatively lower bleeding risk profile in mRCC treatment.
- All reviewed trials were of high quality, supporting the reliability of the findings.
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