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Surgery With or Without Combination Chemotherapy in Treating Patients With Cancer of the Esophagus

Primary Purpose

Esophageal Cancer, Gastric Cancer

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
cisplatin
fluorouracil
adjuvant therapy
conventional surgery
neoadjuvant therapy
Sponsored by
UNICANCER
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Cancer focused on measuring stage I gastric cancer, stage II gastric cancer, stage I esophageal cancer, stage II esophageal cancer, adenocarcinoma of the stomach, adenocarcinoma of the esophagus

Eligibility Criteria

0 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Adenocarcinoma of the lower third of the esophagus or the cardia for which complete resection is feasible Extension to the cardia allowed Cancer of the cardia with extension to the esophagus or stomach allowed No in situ cancer of the cardia No distant metastases PATIENT CHARACTERISTICS: Age: Not over 75 Performance status: WHO 0 or 1 Hematopoietic: WBC at least 4,000 Polymorphonuclear lymphocytes greater than 2,000 Platelets at least 100,000 Hepatic: Not specified Renal: Creatinine less than 1.3 mg/dL (120 micromoles/L) Cardiovascular: No prior myocardial infarction No other cardiac contraindication to surgery Pulmonary: No respiratory contraindication to surgery Other: No second malignancy except: Basal cell carcinoma of the skin Adequately treated in situ carcinoma of the uterine cervix PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy No prior chemotherapy for tumors of the cardia Endocrine therapy No prior radiotherapy for tumors of the cardia Radiotherapy Not specified Surgery Not specified

Sites / Locations

  • Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 1, 1999
Last Updated
February 19, 2021
Sponsor
UNICANCER
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1. Study Identification

Unique Protocol Identification Number
NCT00002883
Brief Title
Surgery With or Without Combination Chemotherapy in Treating Patients With Cancer of the Esophagus
Official Title
A PROSPECTIVE RANDOMISED TRIAL OF INDUCTION CHEMOTHERAPY WITH 5-FU CONTINUOUS IV INFUSION AND CISPLATIN VERSUS SURGERY IN RESECTABLE ADENOCARCINOMA OF THE LOW THIRD OF THE ESOPHAGUS AND CARDIOESOPHAGEAL JUNCTION
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
October 1996 (Actual)
Primary Completion Date
November 2006 (Actual)
Study Completion Date
August 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
UNICANCER

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. It is not known whether combining chemotherapy with surgery is more effective than surgery alone. PURPOSE: Randomized phase III trial to compare the effectiveness of surgery with or without combination chemotherapy in treating patients with cancer of the esophagus.
Detailed Description
OBJECTIVES: Compare survival in patients with operable adenocarcinoma of the lower third of the esophagus or the cardia treated with fluorouracil/cisplatin vs. no chemotherapy prior to surgical resection. Assess whether neoadjuvant fluorouracil/cisplatin increases tumor resectability. OUTLINE: This study is randomized for neoadjuvant chemotherapy. Patients are stratified by performance status, tumor location, and randomizing center. Patients randomized to no neoadjuvant chemotherapy undergo resection of the tumor with adequate margins and resection of regional lymph nodes (R2 with at least 8 nodal groups recommended). Patients randomized to neoadjuvant chemotherapy receive fluorouracil and cisplatin at 3-4 week intervals; fluorouracil is given by continuous intravenous infusion for 5 days and cisplatin is given on the first 2 days of fluorouracil administration. Tumor response is assessed after 2 courses; responding patients with no serious toxicity receive a third course. Surgery, as above, is initiated 4-6 weeks after the second or third course of chemotherapy. Upon recovery (within 3-6 weeks), patients who responded to neoadjuvant chemotherapy receive 3-4 additional courses of postoperative chemotherapy (maximum total of 6 courses). Patients whose best response was stable disease are assessed for postoperative radiotherapy. Patients on either arm with positive resection margins, positive lymph nodes, or equivocal complete resection are referred for postoperative radiotherapy. Further therapy for patients with incomplete resection is at the discretion of the physician. Patients are followed every 3-4 months for at least 5 years. PROJECTED ACCRUAL: A total of 250 patients will be entered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Cancer, Gastric Cancer
Keywords
stage I gastric cancer, stage II gastric cancer, stage I esophageal cancer, stage II esophageal cancer, adenocarcinoma of the stomach, adenocarcinoma of the esophagus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
cisplatin
Intervention Type
Drug
Intervention Name(s)
fluorouracil
Intervention Type
Procedure
Intervention Name(s)
adjuvant therapy
Intervention Type
Procedure
Intervention Name(s)
conventional surgery
Intervention Type
Procedure
Intervention Name(s)
neoadjuvant therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Adenocarcinoma of the lower third of the esophagus or the cardia for which complete resection is feasible Extension to the cardia allowed Cancer of the cardia with extension to the esophagus or stomach allowed No in situ cancer of the cardia No distant metastases PATIENT CHARACTERISTICS: Age: Not over 75 Performance status: WHO 0 or 1 Hematopoietic: WBC at least 4,000 Polymorphonuclear lymphocytes greater than 2,000 Platelets at least 100,000 Hepatic: Not specified Renal: Creatinine less than 1.3 mg/dL (120 micromoles/L) Cardiovascular: No prior myocardial infarction No other cardiac contraindication to surgery Pulmonary: No respiratory contraindication to surgery Other: No second malignancy except: Basal cell carcinoma of the skin Adequately treated in situ carcinoma of the uterine cervix PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy No prior chemotherapy for tumors of the cardia Endocrine therapy No prior radiotherapy for tumors of the cardia Radiotherapy Not specified Surgery Not specified
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Ychou, MD, PhD
Organizational Affiliation
Institut du Cancer de Montpellier - Val d'Aurelle
Official's Role
Study Chair
Facility Information:
Facility Name
Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle
City
Montpellier
ZIP/Postal Code
34298
Country
France

12. IPD Sharing Statement

Citations:
Citation
Boige V, Pignon J, Saint-Aubert B, et al.: Final results of a randomized trial comparing preoperative 5-fluorouracil (F)/cisplatin (P) to surgery alone in adenocarcinoma of stomach and lower esophagus (ASLE): FNLCC ACCORD07-FFCD 9703 trial. [Abstract] J Clin Oncol 25 (Suppl 18): A-4510, 200s, 2007.
Results Reference
result
Citation
Ychou M, Pignon JP, Lasser P, et al.: Phase III preliminary results of preoperative fluorouracil (F) and cisplatin (P) versus surgery alone in adenocarcinoma of stomach and lower esophagus (ASLE): FNLCC 94012-FFCD 9703 trial. [Abstract] J Clin Oncol 24 (Suppl 18): A-4026, 2006.
Results Reference
result

Learn more about this trial

Surgery With or Without Combination Chemotherapy in Treating Patients With Cancer of the Esophagus

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