Skip to content

The outcome of gemcitabine and S1 combination in the treatment of inoperable hilar cholangiocarcinoma

The outcome of gemcitabine and S1 combination in the treatment of inoperable hilar cholangiocarcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004733
Enrollment
Unknown
Registered
2014-03-25
Start date
2009-02-05
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hilar cholangiocarcinoma

Interventions

S-1 alone:S1 was used alone twice daily on days 28 days, followed by a 14-day rest period
Gemcitable+5FU:Gemcitabine 1000 mg/m2 on day 1 and 15 for 4 weeks, combined with 5FU injected intravenously on day 1 and 15 for weeks at a dose of 750mg/person
gemcitable+S1:Gemcitabine intravenously at 1000 mg/m2 on days 1 and 15 and S-1 oral twice daily for 2 weeks followed by a 2-week rest between each 4-week cycle

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
34 Years to 71 Years

Inclusion criteria

Inclusion criteria: 1. Hilar cholangiocarcinoma diagnosed by pathological examination or typical radiographic findings; 2. Unresectable locally advanced or metastatic disease; 3. No prior treatment for hilar cholangiocarcinoma includign surgery or radiation therapy; 4. Age>18 years; 5. To be able to oral intake the chemotherapy drugs.

Exclusion criteria

Exclusion criteria: 1. Severe complications, such as active infection, cardiac or renal disease, marked pleural effusion, or ascites; 2. Active gastrointeatinal bleeing; 3. Severe drug hypersensitivity; 4. Active concomitant malignancy; and 5. Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Leukocyte;

Countries

China

Contacts

Public ContactGuangwen Zhou

Shanghai Jiao Tong University School of Medicine

gwzhousfph@163.com+86 13916662683

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 2, 2026