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A Phase I Study of Adjuvant Chemotherapy With GC in Biliary Tract Cancer Undergoing Resection Without Major Hepatectomy

Primary Purpose

Biliary Tract Cancer

Status
Completed
Phase
Phase 1
Locations
Japan
Study Type
Interventional
Intervention
gemcitabine , cisplatin
Sponsored by
Kansai Hepatobiliary Oncology Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Biliary Tract Cancer

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Biliary tract cancer (BTC) with more than stage IB
  2. BTC undergoing R0 or R1 resection without major hepatectomy
  3. Older than 20 years old
  4. PS0 or 1
  5. No treatment other than surgery
  6. No dysfunction of main organs
  7. Possible oral intake
  8. Treatment start; after 4 weeks and within 12 weeks after surgery
  9. Obtained written informed consent

Exclusion Criteria:

  1. Patients with resection of major hepatectomy
  2. Patients with double cancers
  3. Patients having severe allergy
  4. Patients with severe organ dysfunction
  5. Patients with active infectious disease
  6. Pregnancy
  7. Patients with severe psychological disease
  8. Patients seem inadequate for this study by investigators

Sites / Locations

  • Kobe University Graduate School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

gemcitabine , cisplatin

Arm Description

Outcomes

Primary Outcome Measures

Maximum tolerated dose
To establish the maximum tolerated dose of gemcitabine plus cisplatin in patients with biliary tract cancer undergoing curative resection without major hepatectomy

Secondary Outcome Measures

Number of Participants with dose limiting toxicity
Dose limiting toxicity is defined as follows Grade 4 neutropenia, thrombocytopenia Grade 3 or 4 febrile neutropenia Grade 3 or 4 non-hematological adverse events unless unresponsive to treatment Any adverse events resulting in interruption of dosing on day 8 in both the two courses Any adverse events resulting in dose modification or delay of longer than 2 week

Full Information

First Posted
February 7, 2011
Last Updated
November 13, 2017
Sponsor
Kansai Hepatobiliary Oncology Group
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1. Study Identification

Unique Protocol Identification Number
NCT01297998
Brief Title
A Phase I Study of Adjuvant Chemotherapy With GC in Biliary Tract Cancer Undergoing Resection Without Major Hepatectomy
Official Title
A Phase I Study of Adjuvant Chemotherapy With Gemcitabine Plus Cisplatin in Patients With Biliary Tract Cancer Undergoing Curative Resection Without Major Hepatectomy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2014
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kansai Hepatobiliary Oncology Group

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To decide maximum tolerated dose and recommended dose of treatment using gemcitabine plus cisplatin combination therapy in patients with biliary tract cancer undergoing resection without major hepatectomy.
Detailed Description
Surgery currently remains the only potentially curative treatment for biliary tract cancer (BTC), and most patients develop recurrence. Therefore, effective adjuvant chemotherapy is required to increase the curability of surgery and to prolong the survival in these patients. However, to date, no standard adjuvant chemotherapy has been established, and a guideline for BTC treatment recommends that trials of adjuvant chemotherapy be carried out. Based on results from clinical studies in unresectable BTC, gemcitabine, platinum agent, fluoropyrimidine are considered to have activity against BTC. These agents are expected to be effective in the postoperative adjuvant therapy for BTC, Thus, randomized controlled trials with gemcitabine are ongoing, and the results are expected. Recently, in the ABC-02 study, the first prospective multicenter phase III study in patients with unresectable BTC, gemcitabine/cisplatin combination chemotherapy was compared with gemcitabine monotherapy and showed that the combination therapy significantly prolonged MST (from 8.1 to 11.7 months; P < 0.001). Gemcitabine/cisplatin combination therapy is now considered to be the standard regimen for unresectable BTC, and we expect this regimen to be effective for postoperative adjuvant therapy. Though hepatectomy is frequently performed in surgery for BTC, it is unclear that the effect of anticancer agent is affected by hepatectomy. Because gemcitabine is metabolized by cytidine deaminase primarily in the liver, it considered to have decreased the metabolic ability of gemcitabine after hepatectomy. Some clinical studies demonstrated that patient with hepatectomy could not tolerate the standard dose and schedule of gemcitabine. In the adjuvant chemotherapy with gemcitabine, it is necessary to examine separately whether hepatectomy was undergone or not. In this study, we aimed to assess the safety and efficacy of gemcitabine/cisplatin combination chemotherapy in patients with biliary tract cancer undergoing curative resection without hepatectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biliary Tract Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
gemcitabine , cisplatin
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
gemcitabine , cisplatin
Other Intervention Name(s)
Gemcitabine;gemzer,Cisplatin;Cispulan
Intervention Description
Dose of gemcitabine and cisplatin and treatment schedule
Primary Outcome Measure Information:
Title
Maximum tolerated dose
Description
To establish the maximum tolerated dose of gemcitabine plus cisplatin in patients with biliary tract cancer undergoing curative resection without major hepatectomy
Time Frame
Within 2 courses (every 2 weeks in Level -2 and -1; every 3 weeks in Level 0 and 1)
Secondary Outcome Measure Information:
Title
Number of Participants with dose limiting toxicity
Description
Dose limiting toxicity is defined as follows Grade 4 neutropenia, thrombocytopenia Grade 3 or 4 febrile neutropenia Grade 3 or 4 non-hematological adverse events unless unresponsive to treatment Any adverse events resulting in interruption of dosing on day 8 in both the two courses Any adverse events resulting in dose modification or delay of longer than 2 week
Time Frame
At the end of adjuvant chemotherapy (6 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Biliary tract cancer (BTC) with more than stage IB BTC undergoing R0 or R1 resection without major hepatectomy Older than 20 years old PS0 or 1 No treatment other than surgery No dysfunction of main organs Possible oral intake Treatment start; after 4 weeks and within 12 weeks after surgery Obtained written informed consent Exclusion Criteria: Patients with resection of major hepatectomy Patients with double cancers Patients having severe allergy Patients with severe organ dysfunction Patients with active infectious disease Pregnancy Patients with severe psychological disease Patients seem inadequate for this study by investigators
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tetsuo Ajiki, MD, PhD
Organizational Affiliation
Kobe University Graduate School of Medicine
Official's Role
Study Director
Facility Information:
Facility Name
Kobe University Graduate School of Medicine
City
Kobe
ZIP/Postal Code
650-0017
Country
Japan

12. IPD Sharing Statement

Citations:
PubMed Identifier
24614947
Citation
Toyoda M, Ajiki T, Fujiwara Y, Nagano H, Kobayashi S, Sakai D, Hatano E, Kanai M, Nakamori S, Miyamoto A, Tsuji A, Kaihara S, Ikoma H, Takemura S, Toyokawa H, Terajima H, Morita S, Ioka T. Phase I study of adjuvant chemotherapy with gemcitabine plus cisplatin in patients with biliary tract cancer undergoing curative resection without major hepatectomy (KHBO1004). Cancer Chemother Pharmacol. 2014 Jun;73(6):1295-301. doi: 10.1007/s00280-014-2431-y. Epub 2014 Mar 11.
Results Reference
derived

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A Phase I Study of Adjuvant Chemotherapy With GC in Biliary Tract Cancer Undergoing Resection Without Major Hepatectomy

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