RecruitingPhase 2NCT06607276

Phase 2 Trial of Adjuvant Adebrelimab Combined With Capecitabine in High-Risk Resected Cholangiocarcinoma: ACHIEVE

A Phase 2, Randomized, Controlled, Multicenter Study of Adjuvant Adebrelimab Combined With Capecitabine in Resected Cholangiocarcinoma With High-risk Factors: ACHIEVE


Sponsor

The First Affiliated Hospital with Nanjing Medical University

Enrollment

122 participants

Start Date

Sep 20, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Biliary tract malignancies (BTC) are malignant tumors that originate from the epithelium of the bile ducts. Currently, the optimal treatment for biliary tract malignancies is radical surgical resection. In recent years, with the advancement of imaging technology and surgical techniques, there has been certain progress in the diagnosis and treatment of biliary tract malignancies. However, the surgical resection rate and long-term survival rate after surgery are still not satisfactory, and the high postoperative recurrence rate is an important factor affecting the long-term survival of patients. Therefore, there is an urgent need to explore new postoperative adjuvant treatment plans to reduce postoperative tumor recurrence, which is of great significance for extending the survival of patients with biliary tract malignancies. In the NCCN and CSCO guidelines, capecitabine is listed as a category I recommendation for adjuvant treatment of biliary tract malignancies (BTC). However, in clinical practice, the use of capecitabine or tegafur for postoperative patients with cholangiocarcinoma at high risk of recurrence still has a high recurrence rate. Therefore, there is still a huge unmet need in the clinical adjuvant treatment after surgery for biliary tract malignancies. Based on the above background, we plan to carry out a randomized, open, and comparative study to observe the efficacy and safety of Adebrelimab combined with capecitabine for adjuvant treatment in patients with biliary tract malignancies after surgery, and to explore treatment methods to improve the efficacy of postoperative adjuvant treatment for cholangiocarcinoma.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This phase 2 trial tests whether combining an immunotherapy drug (adebrelimab) with a chemotherapy pill (capecitabine) after surgery reduces the chance of bile duct cancer (cholangiocarcinoma) coming back in patients who had their tumor fully removed but are at high risk of recurrence. **You may be eligible if...** - You are between 18 and 75 years old - You have been diagnosed with cholangiocarcinoma (bile duct cancer), either inside or at the junction of the liver, confirmed by pathology - You had complete surgical removal of the tumor (R0 resection) with high-risk features for recurrence - There is no evidence of cancer recurrence on imaging within the past 28 days - You have not received any prior chemotherapy or radiation for this cancer - You are in good physical condition (ECOG score 0 or 1) **You may NOT be eligible if...** - You have evidence of recurrent or metastatic disease - You have had prior systemic treatment for this cancer - You do not meet liver, kidney, and blood function requirements Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAdebrelimab and capecitabine

Adebrelimab: 1200mg, IV, q3w for one year; capecitabine:1250mg/m2, po, bid,d1-14, q3w, for 6-8 cycles

DRUGcapecitabine

capecitabine:1250mg/m2, po, bid,d1-14, q3w, for 6-8 cycles


Locations(4)

Jinling Hospital

Nanjing, Jiangsu, China

The First Affiliated Hospital of Nanjing Medical University

Nanjing, Jiangsu, China

The Affiliated Hospital of Xuzhou Medical University

Xuzhou, Jiangsu, China

Yancheng NO.1 People's Hospital

Yancheng, Jiangsu, China

View Full Details on ClinicalTrials.gov

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NCT06607276


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