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Neoadjuvant Epirubicin, Cisplatin and Capecitabine (ECX) Followed by Definitive Chemoradiation With/Without Surgery for Squamous Cell Carcinoma of the Oesophagus

Primary Purpose

Oesophageal Carcinoma

Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Epirubicin, Cisplatin, Capecitabine
Surgical Resection
Sponsored by
Royal Marsden NHS Foundation Trust
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Oesophageal Carcinoma

Eligibility Criteria

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

Inclusion Criteria: Age > 18 years. Histologically verified squamous cell carcinoma of the cervical or thoracic oesophagus American Joint Committee on Cancer (AJCC) Stage I-III (T1-3 N0-1 M0) (33), as assessed by spiral or multi-slice computed tomography (CT) and endoscopic ultrasound, where radical chemoradiation would be considered with curative intent. No previous chemotherapy, radiotherapy or other investigational drug treatment for this indication. World Health Organization (WHO) performance status 0,1 or 2. Adequate bone marrow function with platelets > 100 x 10^9/l; white blood cells (WBC) > 3 x 10^9/l; neutrophils > 1.5 x 10^9/l at the time of study entry. Serum bilirubin < 35 micromol/l. Serum creatinine < 180 micromol/l and measured creatinine clearance over 60 ml/min. No concurrent uncontrolled medical condition. No previous malignant disease other than non-melanotic skin cancer or carcinoma in situ of the uterine cervix in the last 10 years. Life expectancy > 3 months. Adequate contraceptive precautions if relevant. Informed written consent. Exclusion Criteria: The presence of locally advanced or metastatic disease precluding curative chemoradiation (T4 or Stage IV or M1a-b) or disease not encompassable in a radical radiotherapy field. Total dysphagia (O'Rourke's swallowing function scoring system 5) precluding swallowing of capecitabine even when crushed. Medical or psychiatric conditions that compromise the patient's ability to give informed consent. Intracerebral metastases or meningeal carcinomatosis. New York Heart Association classification Grade III or IV. Uncontrolled angina pectoris. Pregnancy or breast feeding. Impaired renal function with measured creatinine clearance less than 60 ml/min. Previous investigational study drug Known malabsorption syndromes Patients with a known hypersensitivity to fluorouracil (5-FU) or with a dihydropyrimidine dehydrogenase (DPD) deficiency Hearing loss

Sites / Locations

  • Royal Marsden Hospital

Outcomes

Primary Outcome Measures

2 year overall survival

Secondary Outcome Measures

Objective clinical response rate assessed by computed tomography (CT), endoscopic ultrasound (EUS) and endoscopic biopsy
Pattern of treatment failure
Progression free survival
Proportion of patients not achieving clinical complete response and requiring surgery after chemoradiation
Treatment related toxicity
Time to improvement of dysphagia

Full Information

First Posted
September 19, 2005
Last Updated
December 15, 2009
Sponsor
Royal Marsden NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00220129
Brief Title
Neoadjuvant Epirubicin, Cisplatin and Capecitabine (ECX) Followed by Definitive Chemoradiation With/Without Surgery for Squamous Cell Carcinoma of the Oesophagus
Official Title
Neoadjuvant Epirubicin, Cisplatin and Capecitabine (Xeloda) [ECX] Followed by Definitive Chemoradiation With or Without Surgery for Patients With Newly Diagnosed Localized Squamous Cell Carcinoma of the Oesophagus
Study Type
Interventional

2. Study Status

Record Verification Date
December 2009
Overall Recruitment Status
Completed
Study Start Date
November 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Royal Marsden NHS Foundation Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a study to investigate the efficacy and safety of epirubicin, cisplatin and capecitabine (ECX) as neoadjuvant therapy prior to radical chemoradiotherapy using capecitabine and cisplatin as radio-sensitisers in patients with newly diagnosed localized squamous cell carcinoma of the oesophagus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oesophageal Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Epirubicin, Cisplatin, Capecitabine
Intervention Type
Procedure
Intervention Name(s)
Surgical Resection
Primary Outcome Measure Information:
Title
2 year overall survival
Secondary Outcome Measure Information:
Title
Objective clinical response rate assessed by computed tomography (CT), endoscopic ultrasound (EUS) and endoscopic biopsy
Title
Pattern of treatment failure
Title
Progression free survival
Title
Proportion of patients not achieving clinical complete response and requiring surgery after chemoradiation
Title
Treatment related toxicity
Title
Time to improvement of dysphagia

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years. Histologically verified squamous cell carcinoma of the cervical or thoracic oesophagus American Joint Committee on Cancer (AJCC) Stage I-III (T1-3 N0-1 M0) (33), as assessed by spiral or multi-slice computed tomography (CT) and endoscopic ultrasound, where radical chemoradiation would be considered with curative intent. No previous chemotherapy, radiotherapy or other investigational drug treatment for this indication. World Health Organization (WHO) performance status 0,1 or 2. Adequate bone marrow function with platelets > 100 x 10^9/l; white blood cells (WBC) > 3 x 10^9/l; neutrophils > 1.5 x 10^9/l at the time of study entry. Serum bilirubin < 35 micromol/l. Serum creatinine < 180 micromol/l and measured creatinine clearance over 60 ml/min. No concurrent uncontrolled medical condition. No previous malignant disease other than non-melanotic skin cancer or carcinoma in situ of the uterine cervix in the last 10 years. Life expectancy > 3 months. Adequate contraceptive precautions if relevant. Informed written consent. Exclusion Criteria: The presence of locally advanced or metastatic disease precluding curative chemoradiation (T4 or Stage IV or M1a-b) or disease not encompassable in a radical radiotherapy field. Total dysphagia (O'Rourke's swallowing function scoring system 5) precluding swallowing of capecitabine even when crushed. Medical or psychiatric conditions that compromise the patient's ability to give informed consent. Intracerebral metastases or meningeal carcinomatosis. New York Heart Association classification Grade III or IV. Uncontrolled angina pectoris. Pregnancy or breast feeding. Impaired renal function with measured creatinine clearance less than 60 ml/min. Previous investigational study drug Known malabsorption syndromes Patients with a known hypersensitivity to fluorouracil (5-FU) or with a dihydropyrimidine dehydrogenase (DPD) deficiency Hearing loss
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Cunningham
Organizational Affiliation
Royal Marsden NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Marsden Hospital
City
Sutton
State/Province
Surrey
ZIP/Postal Code
SM2 5PT
Country
United Kingdom

12. IPD Sharing Statement

Learn more about this trial

Neoadjuvant Epirubicin, Cisplatin and Capecitabine (ECX) Followed by Definitive Chemoradiation With/Without Surgery for Squamous Cell Carcinoma of the Oesophagus

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