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Surgery With or Without Combination Chemotherapy in Treating Patients With Cancer of the Esophagus
This study is ongoing, but not recruiting participants.
Study NCT00002883   Information provided by National Cancer Institute (NCI)
First Received: November 1, 1999   Last Updated: February 6, 2009   History of Changes

November 1, 1999
February 6, 2009
October 1996
 
 
 
Complete list of historical versions of study NCT00002883 on ClinicalTrials.gov Archive Site
 
 
 
Surgery With or Without Combination Chemotherapy in Treating Patients With Cancer of the Esophagus
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

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.

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.

Phase III
Interventional
Treatment, Randomized
  • Esophageal Cancer
  • Gastric Cancer
  • Drug: cisplatin
  • Drug: fluorouracil
  • Procedure: adjuvant therapy
  • Procedure: conventional surgery
  • Procedure: neoadjuvant therapy
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
250
 
 

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
Both
up to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00002883
 
CDR0000065190, FRE-FNCLCC-94012, EU-96018
Federation Nationale des Centres de Lutte Contre le Cancer
 
Study Chair: Marc Ychou, MD, PhD Centre Val d'Aurelle - Paul Lamarque
National Cancer Institute (NCI)
April 2001

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP