Clinical Study of Adjuvant Surufatinib Therapy for Postop... | NCT07279532

Status Module

Label	Type	Description	Intervention Names
Experimental Group	Experimental	Surufatinib 200mg, administered orally once daily (QD), for 6 months as postoperative adjuvant therapy.	Drug: surufatinib

Name	Type	Description	Arm Group Labels	Other Names
surufatinib	Drug	Surufatinib 200mg, administered orally once daily (QD), for 6 months as postoperative adjuvant therapy.	Experimental Group

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Recurrence Free Survival（RFS）	Refers to the time from when a patient achieves complete response after anticancer therapy or surgery until the occurrence of disease recurrence or death from any cause.	4 years

Secondary Outcomes

Measure	Description	Time Frame
Overall Survival （OS）	Refers to the time from the start of randomization (or the start of treatment in a single-arm trial) until death due to any cause.	4 years
Adverse Event (AE)	In a drug clinical trial, it refers to all adverse medical events that occur in subjects after receiving the investigational medicinal product, which can manifest as symptoms, signs, diseases, or laboratory abnormalities, but are not necessarily causally related to the investigational medicinal product.

Measure	Description	Time Frame
Biomarkers	Concentrations of NSE and ProGRP in blood samples, evaluated as percentage changes at each tumor assessment from baseline to treatment	4 years

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Provide written informed consent and voluntarily participate in the study.
Aged 18-80 years, male or female.
Confirmed as Stage III NET G1/G2 or any-stage NET G3 after surgical treatment.
Other postoperative NET patients deemed by the investigator to have high-risk factors.
Adequate organ function meeting the following criteria (no use of any blood components, cell growth factors, or corrective drugs within 14 days prior to the first dose of the study drug): (i) Absolute Neutrophil Count (ANC) ≥1.5×10⁹/L; (ii) Platelets ≥100×10⁹/L; (iii) Hemoglobin ≥8 g/dL; (iv) Total Bilirubin ≤1.5 × ULN; ALT and AST ≤2.5 × ULN (or ≤5 × ULN if liver metastases are present); (v) Serum Creatinine ≤1.5 × ULN or Creatinine Clearance >60 mL/min (Cockcroft-Gault formula).
Female subjects of childbearing potential must have a negative serum pregnancy test within 72 hours before the first study drug dose and use effective contraception during the study and for at least 3 months after the last dose. Male subjects with female partners of childbearing potential must use effective contraception during the study and for 3 months after the last dose.

Exclusion Criteria:

Major surgery, open biopsy, or significant trauma within 28 days prior to the first dose.
History of severe or poorly controlled interstitial lung disease.
Poorly controlled hypertension (systolic BP ≥140 mmHg or diastolic BP ≥90 mmHg) despite antihypertensive medication.
Poorly controlled cardiovascular diseases, including but not limited to:

(i)NYHA Class II or higher heart failure; (ii) Unstable angina; (iii) Myocardial infarction within the past year; (iv) Clinically significant supraventricular or ventricular arrhythmias poorly controlled with or without intervention.
Significant bleeding tendency or clinically significant bleeding within 3 months prior to the first dose (e.g., gastrointestinal bleeding, hemorrhagic gastric ulcer, vasculitis).
Arterial/venous thrombotic events within 6 months prior to the first dose (e.g., transient ischemic attack, cerebral hemorrhage, cerebral infarction, deep vein thrombosis, pulmonary embolism). Superficial vein thrombosis may be enrolled if deemed eligible by the investigator.
Concurrent active malignancy requiring treatment, except for adequately treated non-melanoma skin cancer or carcinoma in situ of the cervix.
Pregnancy or lactation.
Any other condition deemed by the investigator to potentially lead to study discontinuation (e.g., severe comorbid illnesses, abnormal laboratory values, psychosocial issues).