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UnknownNCT00008047

Combination Chemotherapy Combined With Radiation Therapy in Treating Patients Who Have Stage II or Stage III Cancer of the Esophagus

Multicentre Phase II Study Of Concomitant Radio-Chemotherapy Associating Continuous Infusion 5-FU With Hydroxyuree Via Bone Marrow With Or Without Paclitaxel In Treatment Of Inoperable Epidermoid Carcinoma Of Esophagus

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining more than one chemotherapy drug with radiation therapy may kill more tumor cells. PURPOSE: Randomized phase I/II trial to study the effectiveness of combination chemotherapy with or without paclitaxel combined with radiation therapy in treating patients who have stage II or stage III cancer of the esophagus.

Detailed description

OBJECTIVES: * Compare the efficacy of concurrent radiotherapy with fluorouracil and hydroxyurea with or without paclitaxel in terms of survival without dysphagia in patients with inoperable stage II or III epidermoid carcinoma of the esophagus. * Compare the overall survival, response rate, toxicity, and quality of life in this patient population treated with these regimens. OUTLINE: This is a randomized, open label, multicenter study. Patients are stratified according to weight loss (less than 10% vs at least 10%) and inoperability criteria (nonresectable vs due to anatomical terrain). Patients are randomized to one of two treatment arms. * Arm I: Patients receive fluorouracil IV continuously, oral hydroxyurea, and concurrent radiotherapy daily on days 1-5. * Arm II: Patients receive fluorouracil, hydroxyurea and radiotherapy as in arm I. Patients also receive paclitaxel IV on day 1. Treatment continues every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients with possible resectable disease undergo surgical resection at 4-6 weeks following the last course of chemoradiotherapy. Patients with continued unresectable disease receive 2 additional courses of chemoradiotherapy as above within 8-17 days following the last course of chemoradiotherapy. Quality of life is assessed at baseline, monthly during therapy, every 2 months for 6 months, every 4 months for 1 year, and then every 6 months thereafter. Patients are followed every 2 months for 6 months, every 4 months for 1 year, and then every 6 months thereafter. PROJECTED ACCRUAL: A maximum of 90 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGfluorouracil
DRUGhydroxyurea
DRUGpaclitaxel
PROCEDUREconventional surgery
RADIATIONradiation therapy

Timeline

Start date
1999-08-01
First posted
2003-01-27
Last updated
2009-02-09

Locations

14 sites across 1 country: France

Source: ClinicalTrials.gov record NCT00008047. Inclusion in this directory is not an endorsement.

Combination Chemotherapy Combined With Radiation Therapy in Treating Patients Who Have Stage II or Stage III Cancer of t (NCT00008047) · Clinical Trials Directory