Clinical Feasibility of Nab-paclitaxel Plus Gemcitabine-cisplatin Chemotherapy in Patients With Locally Advanced Cholangiocarcinoma and Discovery of Biomarkers

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The objective of this observational study is to identify patients with locally advanced cholangiocarcinoma treated with nab-paclitaxel and gemcitabine-cisplatin chemotherapy. In this clinical study, peripheral blood and tumor tissues will be analyzed at baseline and every 3 cycles after systemic drug treatment in patients with locally advanced cholangiocarcinoma, and correlation with treatment was analyzed. This is an exploratory study to discover biomarkers that are highly correlated with treatment response.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Those above the age of 19 who understand the purpose of the study and agree to participate in the collection of samples during the study.

• Patients with histologically or cytologically confirmed inoperable locally advanced cholangiocarcinoma (gallbladder cancer, extrahepatic biliary tract cancer, intrahepatic biliary tract cancer)

• Patients who underwent an NGS test with advanced cholangiocarcinoma tissues

• Patients planning to be treated with nab-paclitaxel plus gemcitabine-cisplatin combination therapy

• ECOG performance status 0 or 1

Locations
Other Locations
Republic of Korea
CHA Bundang Medical Center
RECRUITING
Seongnam-si
Contact Information
Primary
Hong Jae Chon, MD,PhD
minidoctor@cha.ac.kr
82-031-780-3928
Time Frame
Start Date: 2023-03-20
Estimated Completion Date: 2024-11-30
Participants
Target number of participants: 100
Treatments
nab-paclitaxel plus gemcitabine-cisplatin
gemcitabine, 800 mg/m2, cisplatin, 25 mg/m2, and nab-paclitaxel, 100 mg/m2, on days 1 and 8 of 21-day cycles
Related Therapeutic Areas
Sponsors
Leads: CHA University

This content was sourced from clinicaltrials.gov