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OncoMatch/Clinical Trials/NCT07640048

Adjuvant Therapy for High-Risk Intrahepatic Cholangiocarcinoma: A Real-World Study

Official title: A Real-World Study on Postoperative Adjuvant Therapy for Intrahepatic Cholangiocarcinoma Patients With High-Risk Recurrence Factors

Is NCT07640048 recruiting? Yes, currently enrolling (Oct 2026). Studying multiple treatments for intrahepatic cholangiocarcinoma (icc).

RecruitingPeking Union Medical College HospitalNCT07640048Data as of Oct 2026Location: China

Treatment: Adebrelimab · Gemcitabine · Cisplatin · S-1 · Apatinib — This multicenter real-world study assesses the efficacy and safety of adjuvant therapies in postoperative intrahepatic cholangiocarcinoma (ICC) patients with high-risk recurrence factors. 90 eligible patients will be assigned to: Cohort 1: GP (gemcitabine/cisplatin) + adebrelimab Cohort 2: Apatinib + adebrelimab Cohort 3: S-1 (tegafur/gimeracil/oteracil) + adebrelimab Outcomes will be compared against historical real-world controls receiving standard chemotherapy.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Adebrelimab

Targeted therapy

Apatinib

Chemotherapy

GemcitabineCisplatin

Other

S-1

Cancer type

Cholangiocarcinoma

Disease stage

Required: Stage ANY T

Any T stage; N0/N+; M0

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

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

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ function.

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

Frequently asked questions

Is NCT07640048 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.

What disease stage is eligible?

Stage ANY T is required.

Could you qualify for this trial?

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

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