[Translation] A retrospective non-interventional study of the efficacy and safety of LANREOTIDE AUTOGEL® at a dose of 120 mg every 28 days in the treatment of patients with gastroenteropancreatic neuroendocrine tumors (GEP-NET) in routine clinical practice in Hong Kong and Taiwan, China
在常规临床实践中进一步描述Lanreotide Autogel在中国华人参试者中用于肿瘤控制单药治疗的临床有效性和安全性,以补充桥接研究并支持临床试验申请。病史记录回顾的是在开始使用Lanreotide Autogel治疗后约48周后的数据。
[Translation] The purpose of this study is to further characterize the clinical efficacy and safety of Lanreotide Autogel as a monotherapy for tumor control in Chinese participants in routine clinical practice to supplement the bridging study and support the clinical trial application. The medical records were reviewed approximately 48 weeks after the start of treatment with Lanreotide Autogel.