Overview

Combination Chemotherapy in Treating Patients With Locally Advanced or Metastatic Cancer of the Pancreas

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 tumor cells from dividing so they stop growing or die. Combining more that one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining gemcitabine and docetaxel in treating patients who have locally advanced or metastatic cancer of the pancreas.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Eastern Cooperative Oncology Group
Collaborator:
National Cancer Institute (NCI)
Treatments:
Docetaxel
Gemcitabine
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma or poorly differentiated
carcinoma of the pancreas Metastatic disease with at least 1 bidimensionally measurable
lesion OR Locally advanced disease that is either recurrent or not amenable to surgery
Measurable disease outside of prior radiation port or disease progression within the port

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: Not
specified Hematopoietic: Absolute neutrophil count at least 1500/mm3 Platelet count at
least 125,000/mm3 Hepatic: Bilirubin no greater than upper limit of normal (ULN) SGOT no
greater than 2.5 times ULN (less than 3 times ULN if liver metastases) Renal: Creatinine no
greater than ULN Other: Not pregnant or nursing Fertile patients must use effective
contraception

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior
chemotherapy for metastatic disease At least 1 year since prior adjuvant chemotherapy Prior
chemoradiotherapy as initial therapy allowed Endocrine therapy: Not specified Radiotherapy:
See Disease Characteristics See Chemotherapy At least 4 weeks since prior radiotherapy
Surgery: Not specified