Surufatinib related nephrotic syndrome in a pancreatic neuroendocrine tumor: a case report and review of literature

Chengqian Shi^1*Jinglian Lin¹Xiadan Xiang¹Wenlong Bao²Jie Yang^1*

• ¹Second Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China
• ²Zhejiang Cancer Hospital, University of Chinese Academy of Sciences, Hangzhou, Zhejiang, China

Pancreatic neuroendocrine tumors (pNETs) are rare, heterogenous neoplasms originating from pancreatic neuroendocrine cells, which regulate hormone secretion and metabolic homeostasis.Pancreatic neuroendocrine tumors (pNETs) are rare malignancies originating from the pancreas. Surgery is the primary method of control and potential cure for pNETs and targeted therapies have also been investigated for low-grade inoperable or distant metastatic pNETs. Surufatinib, an oral angioimmuno kinase inhibitor, is approved for treating inoperable or late-stage, low-grade (G1 and G2), well-differentiated pNETs and extrapancreatic neuroendocrine tumors. This study describes a case of nephrotic syndrome in a middle-aged woman with pNETs. This patient showed nephrotic syndrome after surufatinib treatment 3 months and renal pathology suggested IgA nephropathy with moderate podocyte injury. However, the nephrotic syndrome was relieved after 2 weeks of discontinuation of surufatinib. After resuming treatment with low-dose surufatinib for 2 weeks, the random proteinuria quantification was increased and the proteinuria turned negative after discontinuation of surufatinib again. It provides a reference for surufatinib related nephrotic syndrome in patients with pNETs and the potential mechanism between surufatinib and podocyte injury in IgA nephropathy needs to be investigated.