Overview

Docetaxel Plus Carboplatin in Treating Patients With Advanced Cancer of the Esophagus

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of docetaxel plus carboplatin in treating patients who have advanced cancer of the esophagus.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Eastern Cooperative Oncology Group
Collaborator:
National Cancer Institute (NCI)
Treatments:
Carboplatin
Docetaxel
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed metastatic or incurable, locally advanced
squamous cell carcinoma of the esophagus Measurable disease outside of a previously
radiated field required

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: Not
specified Hematopoietic: Absolute granulocyte count at least 1500/mm3 Platelet count at
least 100,000/mm3 Hepatic: Bilirubin normal SGOT no greater than 2 times upper limit of
normal Renal: Creatinine normal Cardiovascular: No congestive heart failure or angina
pectoris, even if medically controlled No prior myocardial infarction within the past year
No clinically significant conduction system abnormalities, such as 2nd or 3rd degree heart
block or bundle branch block Pulmonary: Not specified Other: Not pregnant or nursing
Fertile patients must use effective contraception No active infections or medical illnesses
that are uncontrolled No second malignancy other than previously treated nonmelanoma skin
cancer or carcinoma in situ of the cervix or a prior malignancy from which patient has been
disease free for past 3 years Caloric intake greater than 1500 calories/day Fluid intake
greater than 1500 mL/day

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior
chemotherapy Endocrine therapy: Not specified Radiotherapy: At least 4 weeks since prior
radiotherapy Surgery: Not specified