Management of metastatic renal cell carcinoma following prior vascular endothelial growth factor-targeted therapy: A real-world retrospective study from Taiwan

被引:4
作者
Chung, Hsiao-Jen [1 ,2 ,3 ]
Chang, Yen-Hwa [1 ,2 ,3 ]
Huang, Yi-Hsiu [1 ,2 ,3 ]
Lin, Tzu-Ping [1 ,2 ,3 ]
Wei, Tzu-Chun [1 ,2 ,3 ]
Lin, Fang-Ju [4 ,5 ,6 ]
Huang, Huai-Hsuan [7 ]
Wang, Hui-Chuan [8 ]
机构
[1] Taipei Vet Gen Hosp, Dept Urol, 201,Sect 2,Shi Pai Rd, Taipei 112, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Coll Med, Dept Urol, Taipei, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Shu Tien Urol Res Ctr, Taipei, Taiwan
[4] Natl Taiwan Univ, Coll Med, Sch Pharm, Grad Inst Clin Pharm, Taipei, Taiwan
[5] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei, Taiwan
[6] Natl Taiwan Univ Hosp, Dept Pharm, 33 Linsen South Rd, Taipei 100, Taiwan
[7] Natl Taiwan Univ Hosp, Dept Internal Med, Div Hematol, Taipei, Taiwan
[8] Ipsen Pharma Taiwan Branch, Taipei, Taiwan
关键词
Metastatic Renal Cell Carcinoma; Real-World; Taiwan; Treatment Patterns; Vascular Endothelial Growth Factor-Targeted Therapy; EVEROLIMUS; EFFICACY;
D O I
10.1097/JCMA.0000000000000701
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There are limited real-world data to guide the sequencing of targeted therapies in patients with metastatic renal cell carcinoma (mRCC). The objective of this study was to characterize real-world treatment patterns (primarily second line [2L]) after prior vascular endothelial growth factor (VEGF) targeted therapy in an unselected mRCC population from Taiwan between 2013 and 2017. Treatment-related adverse events (TRAEs) and their management were also evaluated (NCT03633579). Methods: This retrospective cohort study included patients who had received prior VEGF-targeted therapy and were treated at the National Taiwan University Hospital or the Taipei Veterans General Hospital between June 2013 and December 2017. Outcomes were characterized using descriptive statistics. Results: Overall, 27 patients were included: 22 (81.5%) male; mean standard deviation (SD) age, 63.1 (11.1) years; 18 (66.7%) initiated targeted therapy during the year immediately following mRCC diagnosis. All patients received sunitinib as their first-line (1L) targeted therapy, with a median (range) treatment duration of 10 (1.8-65.8) months. The most common reason for discontinuing 1L sunitinib was disease progression (88.9% of patients). Everolimus was the most common 2L targeted therapy, in 23 patients (85.2%); 4 patients (14.8%) received 2L axitinib. Median (range) duration of 2L therapy was 4.0 (0.1-30.5) months for everolimus and 4.2 (0.5-9.2) months for axitinib. Ten TRAEs were reported among seven patients receiving 2L everolimus: hypertension (n = 5), hand-foot syndrome (n = 2), hyperglycemia (n = 1), renal failure (n = 1), and interstitial pneumonitis (n = 1). The majority (80%) of TRAEs were managed in the outpatient setting. No TRAEs were reported in the axitinib group. Conclusion: Real-world management of patients with mRCC in Taiwan broadly aligned with clinical guidelines and national reimbursement policy at the time of the study. These findings may be a useful reference for assessing the implications of evolving mRCC management approaches in Taiwan.
引用
收藏
页码:438 / 442
页数:5
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