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Prospective Observational Study to Predict the Response of Biliary Tract Tumors to Immunotherapy

Prospective Observational Study on Prediction of Response to First-line Immunotherapy in Patients With Biliary Tract Tumors

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06048289
Enrollment
150
Registered
2023-09-21
Start date
2023-09-14
Completion date
2025-03-31
Last updated
2023-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Biliary Tract Tumor, Cholangiocarcinoma

Brief summary

A prospective, observational study to explore multidimensional biomarkers for predicting the efficacy of immunotherapy In biliary tract tumors

Detailed description

Patient with unresectable advanced or metastatic biliary tract tumors will be enrolled and plan to receive PD-1/PD-L1 inhibitors combined with chemotherapy as first-line treatment. To explore the biomarkers, tumor tissues, acquired from puncture biopsies at baseline, will be collected and investigated by genomic panel sequencing , transcriptome sequencing, and mIHC. Meanwhile, baseline peripheral blood and feces were also collected for detection of plasma proteins, genomes, and metagenomes. Finally, the investigators will analysis and explore predictive biomarkers of immunotherapy in biliary tract tumors.

Interventions

OTHERBlood samples, tumor biopsy specimens will be collected

Blood samples, tumor biopsy specimens at baseline will be collected

Sponsors

Zhejiang Cancer Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Over 18 years old; 2. Imaging evaluation indicates unresectable advanced or metastatic biliary tract tumors (including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder carcinoma); 3. Confirmed as adenocarcinoma by histology; 4. Has not received systemic therapy in the past (patients who have not progressed within six months after the completion of neoadjuvant therapy or adjuvant therapy can be enrolled); 5. At least one measurable lesion according to RECIST 1.1 standard; 6. Plan to receive PD-1/PD-L1 inhibitors combined with chemotherapy as first-line treatment; 7. Sign informed consent, has good compliance and can cooperate with follow-up.

Exclusion criteria

1. Suffering from other active malignant tumors within 5 years or simultaneously; Unable to collect baseline plasma or tissue samples.

Design outcomes

Primary

MeasureTime frameDescription
Identifying predictive biomarkers of immunotherapy response1 yearldentifying predictive biomarkers of immunotherapy response by detecting differences in genome and transcriptome sequencing between responder and non-responder patients

Countries

China

Contacts

Primary ContactJieer Ying, Dr
jieerying@aliyun.com13858195803

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 8, 2026