A Study to Evaluate the Association of Biliary Complications and Treatment Duration in Unresectable BTC Patients
NCT ID: NCT07101874
Last Updated: 2026-01-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1000 participants
OBSERVATIONAL
2025-08-22
2026-02-28
Brief Summary
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Detailed Description
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This is a multi-center, retrospective, observational study of patients receiving first-line systemic therapy as routine clinical care for unresectable BTC in Japan.
The primary objective of this study is to evaluate the association of the occurrence of biliary complication during first-line systemic therapy with time to treatment failure (TTF) in unresectable BTC patients, to test the hypothesis that the occurrence of biliary complications requiring hospitalization during first-line systemic therapy for unresectable BTC as a time-dependent covariate is significantly associated with TTF .
This study is conducted in collaboration with Japan Oncology Network in Hepatobiliary and Pancreas (JON-HBP, https://jon-hbp.org/en/). Approximately 1,000 patients who start the first dose of first-line systemic therapy for unresectable BTC between May 1, 2022, and December 31, 2023, will be enrolled and these patients' data until July 31, 2025 in medical charts will be collected.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
1. Patients who were deemed unamenable to curative resection at the initial diagnosis.
2. Patients who relapsed after curative resection of BTC more than 6 months after the end of adjuvant therapy or after the date of surgery for patients who did not receive adjuvant therapy.
2\. Patients who received first-line systemic therapy for unresectable BTC with the date of the first dose between May 1, 2022, and December 31, 2023. However, patients who received postoperative adjuvant therapy for BTC with R2 resection is not included.
3\. Patients with ECOG performance status 0 or 1 on the most recent assessment date prior to first dose of first-line systemic therapy for unresectable BTC 4. Patients who provided written informed consent form (ICF), in cases where obtaining informed consent is not difficult, or for whom an appropriate opt-out approach was taken at the study site if obtaining informed consent is difficult.
5\. Patients aged 18 years or older at the date of first dose of first-line systemic therapy for unresectable BTC.
6\. Patients who started first-line systemic therapy with physician's expectation of 3 months or longer prognosis at the time of starting systemic therapy.
Exclusion Criteria
2. Combined any locoregional therapy with first-line systemic therapy for unresectable BTC (e.g., radiation therapy, radiofrequency ablation, arterial injection chemotherapy)
3. Patient who participated in clinical trials (interventional studies) of first-line systemic therapy for BTC
4. Active cancers other than unresectable BTC within the past 2 years from the date of the first dose of first-line systemic therapy. The following are exceptions to this criterion:
* Carcinoma in situ or lesions equivalent to carcinoma in situ.
* Intramucosal cancers that are deemed cured by local treatment.
5. Patients who were followed up for less than 3 months after starting first-line systemic therapy for reasons other than TTF events (disease progression, death, or treatment discontinuation).
ALL
No
Sponsors
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Japan Oncology Network in Hepatobiliary and Pancreas (JON-HBP)
UNKNOWN
AstraZeneca
INDUSTRY
Responsible Party
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Locations
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Research Site
Aichi, , Japan
Research Site
Chiba, , Japan
Research Site
Ehime, , Japan
Research Site
Fukuoka, , Japan
Research Site
Fukushima, , Japan
Research Site
Hokkaido, , Japan
Research Site
Hyōgo, , Japan
Research Site
Ishikawa, , Japan
Research Site
Kagawa, , Japan
Research Site
Kanagawa, , Japan
Research Site
Kochi, , Japan
Research Site
Kyoto, , Japan
Research Site
Miyagi, , Japan
Research Site
Nara, , Japan
Research Site
Okayama, , Japan
Research Site
Osaka, , Japan
Research Site
Ōita, , Japan
Research Site
Saitama, , Japan
Research Site
Shizuoka, , Japan
Research Site
Tochigi, , Japan
Research Site
Tokyo, , Japan
Research Site
Wakayama, , Japan
Countries
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Central Contacts
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Other Identifiers
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D4191R00099
Identifier Type: -
Identifier Source: org_study_id
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