Apatinib-Induced Hypertension Correlates with Improved Prognosis in Solid Tumor Patients
- PMID: 40048128
- DOI: 10.1007/s12012-025-09980-8
Apatinib-Induced Hypertension Correlates with Improved Prognosis in Solid Tumor Patients
Abstract
This study evaluated the occurrence of apatinib-induced hypertension and its impact on the prognosis of patients with solid tumors. A retrospective cohort study with prospective follow-up was conducted on 769 patients treated with apatinib from 2014 to 2021 across three hospitals. Patients were categorized into hypertension and non-hypertension groups. The primary outcome was overall survival (OS), with progression-free survival (PFS) as a secondary outcome. Apatinib-induced hypertension occurred in 33.3% of patients and was associated with significantly longer OS (HR 0.40, 95% CI [0.37-0.48], p < 0.0001) and PFS (HR 0.41, 95% CI [0.35-0.49], p < 0.001). Subgroup analysis confirmed these findings in all cancer types, except for PFS in non-small cell lung cancer. Hypertension may serve as a predictive biomarker for improved anti-tumor efficacy.
Keywords: Apatinib; Cardio-oncology; Cardiotoxicity; Hypertension; VEGF inhibitors.
© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Conflict of interests: The authors declare no competing interests. Ethical Approval: The study received approval from the institutional ethics committee. Consent to Participate: This study was conducted in accordance with the Declaration of Helsinki and was approved by the appropriate institutional review board or ethics committee. Informed consent was obtained from all individual participants included in the study. Participants were provided with detailed information regarding the purpose, procedures, potential risks, and benefits of the study. They were assured that their participation was voluntary and that they could withdraw from the study at any time without any consequences. Consent for Publication: All authors consent to the publication of this manuscript in Cardiovascular Drugs and Therapy.
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