OncoMatch/Clinical Trials/NCT07272512
Prospective Multicenter Real-world Study of Surufatinib in Patients With Advanced Neuroendocrine Neoplasms
Is NCT07272512 recruiting? Yes, currently enrolling (May 2026). This Phase 4 trial studies Surufatinib for neuroendocrine tumors.
Treatment: Surufatinib — This is a prospective, multicenter, phase 4, single-arm study designed to evaluate the effectiveness and safety of surufatinib in adult patients with advanced neuroendocrine neoplasms (NENs) treated in routine clinical practice. Approximately 350 patients with histologically or cytologically confirmed advanced NENs and at least one measurable lesion (RECIST 1.1) will receive oral surufatinib, either as monotherapy (300 mg once daily in 4-week cycles) or in combination regimens (250 mg once daily), according to the treating physician's judgment and protocol guidance. Participants will be followed with regular imaging, laboratory tests, cardiac assessments, and patient-reported outcome questionnaires to monitor tumor response, side effects, quality of life, and treatment adherence. The primary outcomes include progression-free survival, objective response rate, disease control rate, and overall survival; safety will be assessed by the type, frequency, and severity of adverse events. The findings are expected to inform standardized, evidence-based use of surufatinib and help optimize individualized treatment strategies for patients with advanced NENs in the real-world setting.
Check if I qualifyExtracted eligibility criteria
Cancer type
Neuroendocrine Tumor
Lab requirements
Blood counts
adequate bone marrow function required
Kidney function
severe renal impairment excluded
Liver function
severe hepatic impairment excluded
Cardiac function
grade III-IV cardiac insufficiency excluded
adequate organ and bone marrow function; severe hepatic/renal impairment excluded; grade III-IV cardiac insufficiency excluded
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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