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Endostar Combined With SBRT and Envafolimab in the Treatment of Advanced Gastrointestinal Tumors
RECRUITINGPhase 2Sponsored by Nanjing First Hospital, Nanjing Medical University
Actively Recruiting
PhasePhase 2
SponsorNanjing First Hospital, Nanjing Medical University
Started2024-02-21
Est. completion2025-06-21
Eligibility
Age18 Years – 75 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06301828
Summary
This is a single-arm, prospective, exploratory clinical study to evaluate the efficacy and safety of endostar combined with stereotactic body radiation therapy (SBRT) and Envafolimab in patients with advanced gastrointestinal cancer after multi-line treatment.
Eligibility
Age: 18 Years – 75 YearsHealthy volunteers accepted
Inclusion Criteria: * 18 to 75 years old, regardless of gender * advanced gastrointestinal tumors confirmed by histopathology or cytology; * patients with gastrointestinal tumors who did not or refused standard treatment at enrollment;Each line of treatment for advanced disease includes one or more drugs for one or more cycles; The pre-permissible treatment was combined with molecular targeted drugs (except endostar); Patients with previous PD-1 treatment were eligible * ECOG-PS score of 0-2 * The main organ function was normal and met the following requirements: Blood routine examination (no blood transfusion within 14 days) : a. HB≥80g/L; b. ANC ≥1.5×109/L; c. PLT ≥60×109/L; ② Biochemical examination should meet the following criteria: a. BIL\<1.5 times the upper limit of normal (ULN); b. ALT and AST\<2.5×ULN; ALT and AST\< 5×ULN,if liver metastasis was present; c. Serum Cr≤1×ULN, endogenous creatinine clearance ≥50ml/min (Cockcroft-Gault formula) * predicted survival time ≥3 months * Patients voluntarily participated in this study and signed the informed consent form (ICF) Exclusion Criteria: * hypertensive patients whose blood pressure could not be reduced to normal range by antihypertensive drugs (systolic blood pressure\>140 mmHg/diastolic blood pressure \>90 mmHg); Patients with ≥ grade Ⅱ coronary artery disease, arrhythmia (including QTc prolongation \> 450 ms in men and \> 470 ms in women) and cardiac insufficiency * patients with active immune diseases * abnormal coagulation function (INR\>1.5×ULN, APTT\>1.5×ULN) with bleeding tendency * symptomatic central nervous system metastasis * pregnant or lactating women * Other patients deemed ineligible for enrollment by the treating physician
Conditions2
CancerGastrointestinal Neoplasms
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Actively Recruiting
PhasePhase 2
SponsorNanjing First Hospital, Nanjing Medical University
Started2024-02-21
Est. completion2025-06-21
Eligibility
Age18 Years – 75 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06301828