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June 1, 2026Cancer Investigation0 citations

Sex-Specific Adverse Events and Cardiovascular Toxicity of Cabozantinib in Renal Cell Carcinoma: A Nine-Year Pharmacovigilance Study

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EBErhao BaoYLY Q LiYYYang Yang

Key Result

Cabozantinib demonstrated a lower overall cardiovascular adverse event signal (ROR 0.70; 95% CI 0.66-0.75) compared with sunitinib (ROR 0.87; 95% CI 0.82-0.91) in renal cell carcinoma.

Key Points

  • This study aims to investigate sex-specific adverse events and cardiovascular toxicity associated with cabozantinib in renal cell carcinoma patients.
  • Retrospective pharmacovigilance study using U.S. FDA Adverse Event Reporting System data from 2016 to 2025.
  • Disproportionality analyses conducted using Reporting Odds Ratio (ROR) and Proportional Reporting Ratio (PRR) to identify safety signals.
  • Sex-specific differences were assessed through a modified 2 × 2 contingency table and time-to-onset analyzed using Weibull distribution modeling.
  • Females reported more gastrointestinal and dermatologic adverse events compared to males, who had higher severe outcomes like acute myocardial infarction.
  • Cabozantinib displayed a lower cardiovascular adverse event signal (ROR = 0.70, 95% CI: 0.66-0.75) relative to sunitinib (ROR = 0.87, 95% CI: 0.82-0.91).
  • The study indicates an early-onset pattern of adverse events.

Study Design

Type

Observational

Structured PICO

Does cabozantinib have a different sex-specific adverse event profile and cardiovascular toxicity compared to sunitinib in patients with renal cell carcinoma?

P
Population
Patients with renal cell carcinoma (RCC) reported in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) from Q2 2016 to Q2 2025
I
Intervention
Cabozantinib
C
Comparator
Sunitinib
O
Outcome
Sex-specific adverse events and cardiovascular toxicitysafety

In a real-world pharmacovigilance study, cabozantinib showed sex-specific safety differences and a comparatively favorable cardiovascular profile compared to sunitinib in patients with renal cell carcinoma.

Main Result

Effect estimate: ROR 0.70 (95% CI 0.66-0.75)

Abstract

BACKGROUND: Cabozantinib is a multi-target tyrosine kinase inhibitor widely used in advanced renal cell carcinoma (RCC). However, real-world evidence regarding its safety profile, particularly sex-specific adverse events (AEs) and cardiovascular toxicity, remains limited. METHODS: A retrospective pharmacovigilance study was performed using data from the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) from Q2 2016 to Q2 2025. Reports listing cabozantinib as the primary suspected drug and RCC as the indication were included. Disproportionality analyses using Reporting Odds Ratio (ROR) and Proportional Reporting Ratio (PRR) were conducted to identify safety signals. Sex-specific differences were evaluated using a modified 2 × 2 contingency table. Time-to-onset (TTO) was assessed with Weibull distribution modeling. Cardiovascular toxicity was further analyzed using standardized MedDRA queries (SMQs) and compared with sunitinib. RESULTS: < 1, indicating an early-onset pattern. Females showed higher reporting of gastrointestinal and dermatologic AEs, while males had higher frequencies of severe outcomes, including acute myocardial infarction. Cabozantinib demonstrated a lower overall cardiovascular AE signal (ROR = 0.70, 95% CI: 0.66-0.75) compared with sunitinib (ROR = 0.87, 95% CI: 0.82-0.91). CONCLUSIONS: This real-world study highlights sex-specific safety differences, early AE onset, and a comparatively favorable cardiovascular profile of cabozantinib, supporting individualized monitoring strategies in RCC treatment.

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Cite This Study

Bao et al. (2026) conducted an observational in Renal cell carcinoma (RCC). Cabozantinib vs. Sunitinib was evaluated on Overall cardiovascular adverse event signal (ROR 0.70, 95% CI 0.66-0.75). Cabozantinib demonstrated a lower overall cardiovascular adverse event signal (ROR 0.70; 95% CI 0.66-0.75) compared with sunitinib (ROR 0.87; 95% CI 0.82-0.91) in renal cell carcinoma.

synapsesocial.com/papers/6a1d21ba02fbce91306379c8https://doi.org/10.1080/07357907.2026.2676988
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