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

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-08-22

Study Completion Date

2026-02-28

Brief Summary

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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. This study attempts to test the hypothesis that the occurrence of biliary complications requiring hospitalization during first-line systemic therapy for unresectable BTC, which is as a time-dependent covariate, affects time to treatment failure (TTF) .

Detailed Description

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The real-world evidence on cancer-related biliary complications during systemic therapy in patients with advanced biliary tract cancers (BTC) in a large population is lacking. The results from this study may reveal the association of biliary complications with treatment duration, provide an overview of the current status of managing them, and clarify the issues to be addressed as a priority in future studies.

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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Biliary Tract Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

1\. Patients diagnosed with "unresectable BTC" who meet any of the following:

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

1. Maintenance dialysis at the date of the first dose of first-line systemic therapy for unresectable BTC.
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).
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Japan Oncology Network in Hepatobiliary and Pancreas (JON-HBP)

UNKNOWN

Sponsor Role collaborator

AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Research Site

Aichi, , Japan

Site Status RECRUITING

Research Site

Chiba, , Japan

Site Status RECRUITING

Research Site

Ehime, , Japan

Site Status RECRUITING

Research Site

Fukuoka, , Japan

Site Status RECRUITING

Research Site

Fukushima, , Japan

Site Status RECRUITING

Research Site

Hokkaido, , Japan

Site Status RECRUITING

Research Site

Hyōgo, , Japan

Site Status RECRUITING

Research Site

Ishikawa, , Japan

Site Status RECRUITING

Research Site

Kagawa, , Japan

Site Status RECRUITING

Research Site

Kanagawa, , Japan

Site Status RECRUITING

Research Site

Kochi, , Japan

Site Status RECRUITING

Research Site

Kyoto, , Japan

Site Status RECRUITING

Research Site

Miyagi, , Japan

Site Status RECRUITING

Research Site

Nara, , Japan

Site Status RECRUITING

Research Site

Okayama, , Japan

Site Status RECRUITING

Research Site

Osaka, , Japan

Site Status RECRUITING

Research Site

Ōita, , Japan

Site Status RECRUITING

Research Site

Saitama, , Japan

Site Status RECRUITING

Research Site

Shizuoka, , Japan

Site Status RECRUITING

Research Site

Tochigi, , Japan

Site Status RECRUITING

Research Site

Tokyo, , Japan

Site Status RECRUITING

Research Site

Wakayama, , Japan

Site Status RECRUITING

Countries

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Japan

Central Contacts

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AstraZeneca Clinical Study Information Center

Role: CONTACT

1-877-240-9479

Other Identifiers

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D4191R00099

Identifier Type: -

Identifier Source: org_study_id

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