Incidence and risk of hypertension associated with vascular endothelial growth factor receptor tyrosine kinase inhibitors in cancer patients: a comprehensive network meta-analysis of 72 randomized controlled trials involving 30013 patients

被引:45
作者
Liu, Bo [1 ,3 ]
Ding, Fengxia [2 ,3 ]
Liu, Yang [1 ,3 ]
Xiong, Geng [1 ,4 ]
Lin, Tao [1 ]
He, Dawei [1 ]
Zhang, Yuanyuan [4 ]
Zhang, Deying [1 ,3 ]
Wei, Guanghui [1 ]
机构
[1] Chongqing Med Univ, Childrens Hosp, Dept Urol, Chongqing, Peoples R China
[2] Chongqing Med Univ, Childrens Hosp, Dept Resp Med, Chongqing, Peoples R China
[3] Chongqing Int Sci & Technol Cooperat Ctr Child De, Chongqing Key Lab Pediat, Minist Educ, Key Lab Child Dev & Disorders, Chongqing, Peoples R China
[4] Wake Forest Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC USA
关键词
meta-analysis; cancer; VEGFR-TKIs; hypertensive events; CELL LUNG-CANCER; PHASE-III TRIAL; METASTATIC COLORECTAL-CANCER; DIFFERENTIATED THYROID-CANCER; VANDETANIB PLUS DOCETAXEL; PLACEBO-CONTROLLED-TRIAL; DOUBLE-BLIND; 1ST-LINE TREATMENT; HEPATOCELLULAR-CARCINOMA; OPEN-LABEL;
D O I
10.18632/oncotarget.11813
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Tyrosine kinase inhibitors (TKIs) have been developed during the last decade that target the vascular endothelial growth factor receptor (VEGFR) are currently being evaluated as treatments for malignant tumors. The increased application of VEGFR-TKIs means that the probability of hypertension is a serious concern. However, the reported incidence varies markedly between clinical trials. Here, we undertook an up-to-date, comprehensive meta-analysis on clinical works to build the incidence of hypertension along with VEGFR-TKIs. The goal was to understand better of the overall venture of cancer patients' hypertension treated with these drugs. Methods: Databases (EMBASE, PubMed, and Cochrane library) and the abstracts of the American Society of Clinical Oncology annual meeting and European Society of Medical Oncology were searched to identify related studies. 95% confidence intervals (CIs), summary incidences, and relative risk (RR) were calculated utilizing either fixed-effects models on the basis of the heterogeneity of the included studies or random-effects. Results: Seventy-two randomized controlled trials (including 30013 patients) were involved. The total incidence of high-grade and all-grade hypertensive events along with VEGFR-TKIs was 23.0% (95% CI, 20.1-26.0%) and 4.4% (95% CI, 3.7-5.0%), respectively. The use of VEGFR-TKIs remarkably enhanced the venture of developing high-grade (RR, 4.60; 95% CI, 3.92-5.40; P<0.001) and all-grade (RR, 3.85; 95% CI, 3.37-4.40; P<0.001) hypertensive events. Subgroup analyses revealed that the risk of a hypertensive event varied significantly in accordance with tumor type, VEGFR-TKI, trial phase, VEGFR-TKIs-based regimen, control therapy, and chemotherapy regimen. Conclusions: Patients with cancer that receive VEGFR-TKIs are at a remarkable venture of developing hypertension. Therefore, suitable treatment and monitoring should be introduced to avoid cardiovascular complications.
引用
收藏
页码:67661 / 67673
页数:13
相关论文
共 102 条
[1]   Doxorubicin Plus Sorafenib vs Doxorubicin Alone in Patients With Advanced Hepatocellular Carcinoma A Randomized Trial [J].
Abou-Alfa, Ghassan K. ;
Johnson, Philip ;
Knox, Jennifer J. ;
Capanu, Marinela ;
Davidenko, Irina ;
Lacava, Juan ;
Leung, Thomas ;
Gansukh, Bolorsukh ;
Saltz, Leonard B. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2010, 304 (19) :2154-2160
[2]   A randomized, phase II study of vandetanib maintenance for advanced or metastatic non-small-cell lung cancer following first-line platinum-doublet chemotherapy [J].
Ahn, Jin Seok ;
Lee, Ki Hyeong ;
Sun, Jong-Mu ;
Park, Keunchil ;
Kang, Eun-Suk ;
Cho, Eun Kyung ;
Lee, Dae Ho ;
Kim, Sang-We ;
Lee, Gyeong-Won ;
Kang, Jin-Hyoung ;
Lee, Jong-Seok ;
Lee, Jae-Won ;
Ahn, Myung-Ju .
LUNG CANCER, 2013, 82 (03) :455-460
[3]   Incidence and risk of significantly raised blood pressure in cancer patients treated with bevacizumab: an updated meta-analysis [J].
An, Mao Mao ;
Zou, Zui ;
Shen, Hui ;
Liu, Ping ;
Chen, Meng Li ;
Cao, Yong Bing ;
Jiang, Yuan Ying .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 66 (08) :813-821
[4]  
[Anonymous], J CLIN ONCOL
[5]  
[Anonymous], J CLIN ONCOL
[6]  
[Anonymous], 2016, LANCET, DOI DOI 10.1016/S0140-6736(16)00559-6
[7]  
[Anonymous], RANDOMIZED PHASE 3 S
[8]  
[Anonymous], J CLIN ONCOL
[9]  
[Anonymous], NEW ENGL J MED
[10]  
[Anonymous], LANCET