Biomarker Discovery in Patients With Advanced Biliary Tract Cancer

  • STATUS
    Recruiting
  • End date
    Mar 31, 2023
  • participants needed
    100
  • sponsor
    CHA University
Updated on 13 August 2021
paclitaxel
cancer
gemcitabine

Summary

Biliary tract cancer is a rare gastrointestinal malignant neoplasm and includes intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gall bladder cancer. Curative surgical resection offers the only chance for cure. However, most patients with BTC are diagnosed at an unresectable stage. Therefore, the survival outcomes of patients with advanced biliary tract cancer remain dismal.

The combination of gemcitabine and cisplatin has become the current standard for advanced BTCs since the landmark ABC-02 trial in 2010. However, the median overall survival of Gem/Cis chemotherapy is less than 1 year. Recently, a triplet regimen of gemcitabine, cisplatin, and nab-paclitaxel showed promising results in a single-arm phase II multicenter study.

However, biliary tract cancer is a group of heterogenous diseases by site and genetic alteration, and this diversity may lead differences in response to systemic chemotherapy.

Transcriptome analysis through RNA-sequencing has rarely been performed in advanced biliary tract cancer, and even if it has performed, only small number of patients were included. Further research on multi-omics data is needed on the necessity and clinical significance in treatment of biliary tract cancer.

Description

Using biopsy specimen (formalin fixed paraffin embedded tissue), in-house NGS and RNA-sequencing will be performed simultaneously. Through this, investigators will discover biomarkers based on multi-omics data that predict response to systemic chemotherapy (nab-paclitaxel plus gemcitabine-cisplatin). In addition, blood sampling will be performed in parallel to conduct research on cell-free DNA and circulating tumor cell analysis related to response and progression on chemotherapy; before administration of chemotherapy, 3 months after chemotherapy, 6 months after chemotherapy, the time of disease progression (if possible), before curative resection (if possible).

Details
Condition Gall Bladder Cancer, Biliary Tract Cancer, Urothelial Tract Cancer, biliary cancer, Biliary neoplasm, gallbladder cancer, Adenocarcinoma, Gall Bladder Disorders, Malignant Adenoma, Gallbladder Disease, Cholangiocarcinoma, Malignant neoplasm of gallbladder, Gallbladder Carcinoma
Treatment nab-paclitaxel plus gemcitabine-cisplatin
Clinical Study IdentifierNCT04871321
SponsorCHA University
Last Modified on13 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 19 years old
Capable of understanding and complying with the protocol requirements and signed informed consent
The patients were confirmed as bilary tract cancer (gall bladder cancer, extrahepatic cholangiocarcinoma, intrahepatic cholangiocarcinoma) by histopathology or cytology
Patients with inoperable or metastatic or recurrent biliary tract cancer
Patients who underwent in-house next-generation sequencing
Patients planning to receive Gemcitabine, Cisplatin, nab-paclitaxel triplet chemotherapy
At least one measurable objective lesion was identified based on the RECIST 1.1 criteria
Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
The expected survival a 3 months

Exclusion Criteria

The subject has uncontrolled, significant intercurrent or recent illness including infection for organ failure
Prior palliative chemotherapy for biliary tract cancer
Dementia, altered mental state, or any mental illness that prevents understanding or informed consent
Other conditions that researchers not think to be suitable for enrollment
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