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Updated: Apr 11, 2026

Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
Effects of Cancer Therapy Targeting Vascular Endothelial Growth Factor Receptor on Central Blood Pressure and
Antonella Moreo1, Paola Vallerio1, Riccardo Ricotta2
1Cardiology IV, "A.De Gasperis" Department, Ospedale Niguarda Ca' Granda, Milan, Italy;
Background:
In the last 2 decades, new drugs that oppose the effects of vascular endothelial growth factor receptor (VEGFR), and thus angiogenesis, have considerably improved treatment of solid tumors. These anti-VEGFR drugs, however, are burdened by several side effects, particularly relevant on heart and vessels. The aim of this study was to analyze the changes in cardiovascular structure and function associated with use of anti-VEGFR drugs.
Methods:
Twenty-nine patients (27 affected by renal and 2 by thyroid cancer), received treatment with anti-VEGFR drugs. Brachial blood pressure (BP), central BP, carotid-femoral pulse wave velocity (cfPWV), augmentation index (Aix), and several echocardiographic markers of systolic and diastolic left ventricular functions including global longitudinal strain were measured before starting treatment (T0), after 2 (T1), and 6 weeks (T2) of treatment.
Results:
Anti-VEGFR treatment was accompanied by a significant increase of both peripheral (systolic BP +13±15.5mm Hg, diastolic BP +7.1±9.3mm Hg, P < 0.001) and central BP (systolic BP +14±14.2mm Hg, diastolic BP +7.3±10.4mm Hg, P < 0.001) and a significant raise of cfPWV (+1.3±1.8 m/sec, P = 0.003). There was also a significant alteration of markers of diastolic and subclinical left ventricular systolic function, including global longitudinal strain (-19.9±3.8% at T0, -17.8±2.6% at T2, P < 0.05). All the changes were already evident at T1, worsened at T2 in patients who maintained oncological treatment, but disappeared at T2 in patients in whom treatment was stopped.
Conclusions:
All the changes regarding BP and cfPWV appear early after treatment initiation and seem to be reversible if treatment is stopped, instead diastolic and systolic left ventricular function are persistently altered by anti-VEGFR drugs.
Insights
Anti-VEGFR drugs significantly increase blood pressure and arterial stiffness, with potential for persistent cardiac dysfunction. Cardiovascular changes are early and may reverse if treatment stops, but left ventricular function alterations persist.
Area of Science:
- Cardiovascular Medicine
- Oncology
- Pharmacology
Background:
- Anti-angiogenic therapies targeting vascular endothelial growth factor receptor (VEGFR) have improved solid tumor treatment.
- These therapies can cause significant cardiovascular side effects.
- This study investigates cardiovascular structural and functional changes during anti-VEGFR drug use.
Purpose of the Study:
- To analyze cardiovascular structural and functional changes in patients treated with anti-VEGFR drugs.
- To assess the impact of anti-VEGFR therapy on blood pressure, arterial stiffness, and left ventricular function.
Main Methods:
- Twenty-nine cancer patients received anti-VEGFR treatment.
- Measurements included brachial and central blood pressure, carotid-femoral pulse wave velocity (cfPWV), augmentation index (Aix), and echocardiographic markers of left ventricular function (including global longitudinal strain).
- Data collected at baseline (T0), 2 weeks (T1), and 6 weeks (T2).
Main Results:
- Significant increases in peripheral and central blood pressure and cfPWV were observed.
- Diastolic and subclinical systolic left ventricular function, including global longitudinal strain, were significantly altered.
- Cardiovascular changes appeared early (T1) and worsened by T2 if treatment continued, but reversed if stopped.
Conclusions:
- Blood pressure and cfPWV changes are early and reversible upon cessation of anti-VEGFR therapy.
- Diastolic and systolic left ventricular function alterations are persistent despite treatment discontinuation.
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