Paclitaxel/Cisplatin/Fluorouracil Followed by Paclitaxel/Cisplatin/Radiotherapy and Esophagectomy for Esophageal Cancer
Primary Purpose
Esophageal Cancer
Status
Unknown status
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
TP-HDFL,TP-CCRT, Esophagectomy
Sponsored by
About this trial
This is an interventional treatment trial for Esophageal Cancer focused on measuring Esophageal cancer, Esophagectomy, Paclitaxel, Induction chemotherapy
Eligibility Criteria
Inclusion Criteria:
- Pathologically proven esophageal cancer
- Locally advanced diseases T3 N0-1 M0; T1-3 N1 M0; T1-3 or N0-1 M1a
- Age ≥ 18 years old
- ECOG ≤ 2
- Creatinine < 1.5 mg/dl AST, ALT < 2.5 x upper normal limits Bilirubin < 2.0 mg/dl
- WBC > 4,000/μl or ANC>2,000/μl
- Platelet > 100,000//μl
- Informed consent
Exclusion Criteria:
- Invasion to surrounding organs (T4 disease)
- Distant mets (except M1a)
- Prior thoracic irradiation
- Presence of other squamous cell carcinoma of aerodigestive way
- Symptomatic co-morbid diseases
- Previous malignancy
Sites / Locations
- National Taiwan University HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
One-cycle induction chemotherapy
Arm Description
TP-HDFL, TP-CCRT, Esophagectomy
Outcomes
Primary Outcome Measures
To determine whether clinical response to one cycle of induction chemotherapy (TP-HDFL) could predict the pathologic complete response to preoperative chemoradiotherapy (TP-CCRT
Secondary Outcome Measures
Full Information
NCT ID
NCT01034332
First Posted
January 7, 2008
Last Updated
December 17, 2009
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01034332
Brief Title
Paclitaxel/Cisplatin/Fluorouracil Followed by Paclitaxel/Cisplatin/Radiotherapy and Esophagectomy for Esophageal Cancer
Official Title
A Phase II Study With One-cycle Weekly TP-HDFL Followed by Twice Weekly TP-CCRT and Esophagectomy for Locally Advanced Esophageal Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
December 2009
Overall Recruitment Status
Unknown status
Study Start Date
December 2007 (undefined)
Primary Completion Date
December 2009 (Anticipated)
Study Completion Date
December 2009 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
We hypothesize that one-cycle induction chemotherapy may also help to identify chemo-responsive esophageal cancer patients who are highly treatable by definitive CCRT.
Detailed Description
We hypothesize that one-cycle induction chemotherapy may also help to identify chemo-responsive esophageal cancer patients who are highly treatable by definitive CCRT.in order to test this hypothesis, we thus propose this phase II clinical study to verify the role of "response to one-cycle induction chemotherapy"in the prediction of pathologic complete response rate to CCRT and tje outcomes for patients with loco-regional esophageal cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Cancer
Keywords
Esophageal cancer, Esophagectomy, Paclitaxel, Induction chemotherapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
58 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
One-cycle induction chemotherapy
Arm Type
Experimental
Arm Description
TP-HDFL, TP-CCRT, Esophagectomy
Intervention Type
Procedure
Intervention Name(s)
TP-HDFL,TP-CCRT, Esophagectomy
Intervention Description
To determine whether clinical response to one cycle of induction chemotherapy (TP-HDFL) could predict the pathologic complete response to preoperative chemoradiotherapy (TP-CCRT) in patients with locally advanced esophageal cancer.
Primary Outcome Measure Information:
Title
To determine whether clinical response to one cycle of induction chemotherapy (TP-HDFL) could predict the pathologic complete response to preoperative chemoradiotherapy (TP-CCRT
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pathologically proven esophageal cancer
Locally advanced diseases T3 N0-1 M0; T1-3 N1 M0; T1-3 or N0-1 M1a
Age ≥ 18 years old
ECOG ≤ 2
Creatinine < 1.5 mg/dl AST, ALT < 2.5 x upper normal limits Bilirubin < 2.0 mg/dl
WBC > 4,000/μl or ANC>2,000/μl
Platelet > 100,000//μl
Informed consent
Exclusion Criteria:
Invasion to surrounding organs (T4 disease)
Distant mets (except M1a)
Prior thoracic irradiation
Presence of other squamous cell carcinoma of aerodigestive way
Symptomatic co-morbid diseases
Previous malignancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chih-Hung Hsu, M.D
Phone
886-2-23711174
Ext
7680
Email
chihhunghsu@ntu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chih-Hung Hsu, M.D
Organizational Affiliation
National Taiwan University Hospita
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
ZIP/Postal Code
100
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chin-Hung Hsu, MD
Phone
02-23123456
Ext
7680
Email
chihhunghsu@ntu.edu.tw
12. IPD Sharing Statement
Citations:
PubMed Identifier
26313683
Citation
Guo JC, Huang TC, Lin CC, Hsieh MS, Chang CH, Huang PM, Lee JM, Hsu FM, Chia-Hsien Cheng J, Wang HP, Yeh KH, Cheng AL, Hsu CH. Postchemoradiotherapy Pathologic Stage Classified by the American Joint Committee on the Cancer Staging System Predicts Prognosis of Patients with Locally Advanced Esophageal Squamous Cell Carcinoma. J Thorac Oncol. 2015 Oct;10(10):1481-9. doi: 10.1097/JTO.0000000000000651.
Results Reference
derived
Learn more about this trial
Paclitaxel/Cisplatin/Fluorouracil Followed by Paclitaxel/Cisplatin/Radiotherapy and Esophagectomy for Esophageal Cancer
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