English Español
Donate
Back to Clinical Trials
Back to Clinical Trials

Brief Title: Adjuvant Chemotherapy for Biliary Tract Cancer After Curative Resection

Adjuvant Chemotherapy With Gemcitabine and Capecitabine Compared to Capecitabine for Biliary Tract Cancer After Curative Resection

INTRODUCTION

  • Org Study ID: EK2017144
  • Secondary ID: N/A
  • NTC ID: NCT03779035
  • Sponsor: Tianjin Medical University Cancer Institute and Hospital

BRIEF SUMMARY


This prospective, open-Label, comparative, randomized, controlled phase III trial was
designed to compare the clinical performance of gemcitabine with capecitabine vs.
capecitabine alone for patients with biliary tract cancer (BTC) after curative resection.

DETAILED DESCRIPTION


Currently, complete surgical resection represents the only potentially curative treatment
option for cholangiocarcinoma (CCA, including intrahepatic, hilar and distal CCA) and
gallbladder carcinoma (GBCA). Because of high rates of disease recurrence and poor survival
rates following surgical resection, postoperative treatment have been considered to improve
patient survival after resection of BTC. The systematic review showed a beneficial impact of
adjuvant treatment in BTC, particularly in patients with involved lymph nodes or resection
margins and distal or hilar CCA. However, in regard of the paucity of randomized data,
current guidelines recommend inclusion in clinical trials.

Previously, the data of the BILCAP trial showed an improvement in median overall survival for
capecitabine compared to observation alone for BTC, indicating capecitabine as the new
standard postoperative treatment after curative resection of BTC.

Previous phase II studies for advanced BTC showed superiority of the combination gemcitabine/
capecitabine regimen vs. the capecitabine monotherapy, the median OS was 12.7-14 vs. 7.9
months.

Based on these data, this AdBTC trial will was designed to compare the clinical performance
of gemcitabine with capecitabine vs. capecitabine alone for patients with biliary tract
cancer (BTC) after curative resection, aiming for superiority of the combination regimen vs.
the oral monotherapy. This will be based on the BILCAP protocol, applying the similar dosing,
assessments and dose modifications.

The primary endpoint is DFS and secondary endpoints include recurrence free survival, OS,
safety and tolerability of adjuvant CTx, quality of life, and patterns of disease recurrence.


  • Overall Status
    Recruiting
  • Start Date
    December 15, 2018
  • Phase
    Phase 3
  • Study Type
    Interventional

PRIMARY OUTCOMES

Primary Outcome 1 - Measure: Disease free survival (DFS) rate

Primary Outcome 1 - Timeframe: at 24 months

CONDITION

  • Cholangiocarcinoma
  • Gall Bladder Carcinoma

ELIGIBILITY


DISEASE CHARACTERISTICS:

- Histologically confirmed biliary tract cancer (including intrahepatic, extrahepatic,
hilar cholangiocarcinoma or muscle invasive gallbladder cancer or cancer of the distal
bile duct)

- Must have undergone a radical surgical approach which includes liver resection,
pancreatic resection, or less commonly both

- Patients with pathological evidence of microscopic involvement of the margins of the
excised specimen are eligible as long as resection is macroscopically complete

- Must be able to start treatment within 12 weeks of surgery

- No pancreatic or periampullary cancer

- No mucosal gallbladder cancer

PATIENT CHARACTERISTICS:

- ECOG performance status 0-2

- Urea < 1.5 times upper limit of normal (ULN)

- Creatinine < 1.5 times ULN

- Glomerular filtration rate ≥ 60 mL/min (if < 60 mL/min, adequate renal function for
capecitabine must be confirmed by isotope EDTA)

- Hemoglobin ≥ 10 g/dL

- WBC ≥ 3,000/mm³

- Absolute neutrophil count ≥ 1,500/mm³

- Platelet count ≥ 100,000/mm³

- Bilirubin ≤ 3 times ULN

- ALT and AST ≤ 5 times ULN

- Adequate surgical biliary drainage with no evidence of infection

- Not pregnant or nursing

- Negative pregnancy test for women of childbearing age and childbearing potential

- Fertile patients must use effective contraception during study treatment and for at
least 3 months after study treatment has ended

- Must provide written informed consent

- No history of other malignant diseases within the past 5 years

- No serious coexisting medical condition likely to interfere with protocol treatment,
including a potential serious infection

- No evidence of significant clinical disorder or laboratory finding that makes it
undesirable for the patient to participate in the trial

- No psychological, familial, sociological, or geographical factors considered likely to
preclude study compliance

- No other serious uncontrolled medical conditions

- No unresolved biliary tree obstruction

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

- Completely recovered from prior surgery

- No use of other investigational agents within 28 days prior to and during study
treatment

- No prior chemotherapy or radiotherapy for biliary tract cancer

- No other concurrent anticancer chemotherapy, radiotherapy, or investigational agent

Gender: All

Minimum Age: N/A

Maximum Age: 18 Years

Healthy Volunteers: No

OFFICIAL INFORMATION

Name: N/A

Role: N/A

Affiliation: N/A

Overall Contact

Name: N/A

Phone: +86-022-23340123

Email: tjchi@hotmail.com

LOCATION

Facility Status Contact
Facility: Tianjin Medical University Cancer Insititute and Hospital
Tianjin, Tianjin 300060
China 		Status: Recruiting Contact:
Tianqiang Song, PH.D.

tjchi@hotmail.com

Read Our Stories