Successful apatinib treatment for advanced clear cell renal carcinoma as a first-line palliative treatment: A case report

被引:1
作者
Wei, Hang-Ping [1 ]
Mao, Jie [2 ]
Hu, Zu-Liang [1 ]
机构
[1] Wenzhou Med Univ, Dongyang Hosp, Dept Med Oncol, 60 West Wuning Rd, Dongyang 322100, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Dongyang Hosp, Dept Radiol, Dongyang 322100, Zhejiang, Peoples R China
关键词
Apatinib; Renal cell carcinoma; Targeted therapy; Palliative treatment; Case report; TARGETED THERAPY; CHEMOTHERAPY;
D O I
10.12998/wjcc.v10.i11.3593
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Apatinib is an orally bioavailable small-molecule receptor tyrosine kinase inhibitor. In December 2014, the China Food and Drug Administration made it the first anti-angiogenic therapy to be approved for treating metastatic gastric cancer. It was specifically designated as a third-line or later treatment for metastatic gastric cancer. CASE SUMMARY Here, we present a case of advanced renal cell carcinoma (RCC) with multiple metastases (Stage IV) in a 48-year-old male with an extremely poor general status (Karnofsky 30%). He was initially given pazopanib as a targeted therapeutic. However, he experienced severe adverse reactions within two weeks, including grade IV oral mucositis. We, thus, tried switching his targeted treatment to an apatinib dose of 250 mg once daily since April 2018. The patient demonstrated striking benefits from this switch to the apatinib palliative treatment. Nearly one month later, his pain and other associated symptoms were alleviated. The patient was able to move freely and had an excellent general status (Karnofsky 90%). His progress has been followed up with regularly, allowing for a documented progression-free survival interval of approximately 32 mo. CONCLUSION This case suggests that, like other multi-target drugs, apatinib may be a useful first-line therapeutic drug for advanced RCC. It may be a particularly helpful curative option when patients are found to be intolerant of other targeted drugs.
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页码:3593 / 3600
页数:8
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