OncoMatch

OncoMatch/Clinical Trials/NCT06349317

Neoadjuvant IMRT Combined With Camrelizumab and Apatinib for Resectable HCC With PVTT

Is NCT06349317 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Neoadjuvant intensity-modulated radiotherapy combined with perioperative camrelizumab and apatinib for hepatocellular carcinoma.

Phase 2RecruitingYongyi ZengNCT06349317Data as of Jun 2026Location: China

Treatment: Neoadjuvant intensity-modulated radiotherapy combined with perioperative camrelizumab and apatinibThis study is an open-label, single-arm prospective clinical trial that evaluates the efficacy and safety of neoadjuvant intensity-modulated radiotherapy combined with perioperative camrelizumab and apatinib in the treatment of resectable hepatocellular carcinoma with portal vein tumor thrombus.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Targeted therapy

Neoadjuvant intensity-modulated radiotherapy combined with perioperative camrelizumab and apatinib

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Lab requirements

Blood counts

ANC ≥1.5×10^9/L; Platelets ≥80×10^9/L; Hemoglobin ≥90g/L

Kidney function

Serum creatinine ≤1.5×ULN, or if >1.5×ULN, creatinine clearance ≥45 mL/min; Urinalysis proteinuria <2+; if baseline proteinuria ≥2+, 24-hour urine protein <1g

Liver function

Total bilirubin ≤3× ULN; ALT and AST ≤5×ULN; Serum albumin ≥30g/L; Child-Pugh Class A

Cardiac function

QTc ≤450ms (males), ≤470ms (females); NYHA class II or above heart failure, LVEF <50%, unstable angina, MI within 1 year, significant arrhythmias excluded

Adequate organ and marrow function, as defined by the following laboratory values: ... Child-Pugh score of Class A; ... QTc > 450ms for males and >470ms for females ... heart failure of NYHA class II or above or echocardiography showing LVEF <50%; unstable angina; myocardial infarction within 1 year before treatment; clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06349317 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify