Key result
Early hypertension within the first 8 weeks of VEGF pathway inhibitor therapy was independently associated with significantly improved progression-free survival (HR 0.61) in patients with advanced solid cancer.
Why the study?
VEGF pathway inhibitors induce cardiovascular adverse events, and while some studies suggest a correlation between efficacy and these adverse events, further real-world evidence was required.
Does the development of cardiovascular adverse events (specifically hypertension) within the first 8 weeks predict improved progression-free survival in patients with advanced solid cancer treated with VEGF pathway inhibitors?
Cohort (n=294)
No
Does the development of cardiovascular adverse events (specifically hypertension) within the first 8 weeks predict improved progression-free survival in patients with advanced solid cancer treated with VEGF pathway inhibitors?
Hazard Ratio: 0.61 (95% CI 0.44–0.84)
Absolute Event Rate: 5.2% vs 2.8%
p-value: p=0.0026
The development of early hypertension in patients receiving VEGF pathway inhibitors for advanced solid cancers is a strong independent predictor of improved progression-free survival.
Objective Many vascular endothelial growth factor (VEGF) pathway inhibitors are used in the treatment of patients with various advanced cancers; however, treatments induce cardiovascular adverse events (CVAEs), such as hypertension, heart failure, arrhythmia, arterial or venous embolism, and hemorrhage. Some studies have suggested a correlation between efficacy and CVAEs; however, further evidence is required. This study evaluated real-world data concerning the frequency and degree of CVAEs and possible associations between CVAEs and efficacy in such patients. Methods We analyzed CVAEs observed in 294 patients with advanced cancer who were treated with ramucirumab, regorafenib, pazopanib, sunitinib, or sorafenib. Results CVAEs of any grade and proteinuria within 8 weeks after the initiation of VEGF pathway inhibitors (early) or during the treatment period (total period) were observed in 72-85% and 77-92% of the patients, respectively. The progression-free survival (PFS) of patients with a CVAE of grade ≥1 in the early period was favorable compared with the PFS of those who had no CVAE (median, 4.9 vs. 3.5 months, p=0.016, log-rank test). Furthermore, the PFS of patients with a CVAE grade ≥3 in the early period was favorable compared to that of those with CVAEs of grades 0-2. Taken together, a higher degree of CVAE was correlated with favorable patient outcomes. Conclusion This study revealed the frequency and degree of CVAEs in patients with solid cancers who received VEGF pathway inhibitors in a real-world setting and added evidence regarding the correlation between CVAEs and efficacy of VEGF pathway inhibitors.
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Yoshida et al. (2024) conducted a cohort in Advanced solid cancer (n=294). Early hypertension (within 8 weeks of VEGF pathway inhibitor initiation) vs. No early hypertension was evaluated on Progression-free survival (PFS) (HR 0.61, 95% CI 0.44-0.84, p=0.0026). Early hypertension within the first 8 weeks of VEGF pathway inhibitor therapy was independently associated with significantly improved progression-free survival (HR 0.61) in patients with advanced solid cancer.
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