Overview

S9924 R115777 in Treating Patients With Locally Advanced or Metastatic Pancreatic Cancer

Status:
Completed
Trial end date:
2005-10-01
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. PURPOSE: Phase II trial to study the effectiveness of R115777 in treating patients who have locally advanced or metastatic pancreatic cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Southwest Oncology Group
Collaborator:
National Cancer Institute (NCI)
Treatments:
Pancreatin
Pancrelipase
Tipifarnib
Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed adenocarcinoma of the
pancreas Ductal adenocarcinoma Mucinous noncystic carcinoma Signet ring cell carcinoma
Adenosquamous carcinoma Undifferentiated (anaplastic) carcinoma Mixed ductal endocrine
carcinoma Well differentiated adenocarcinoma Moderately well or poorly differentiated
adenocarcinoma Undifferentiated ductal carcinoma No papillary cystic carcinomas, sarcomas,
or tumors arising from the endocrine pancreas Pathological confirmation of a metastatic
site allowed Clinical documentation of pancreatic involvement and no evidence of another
primary allowed Locally advanced or distant metastatic disease surgically incurable No
known brain metastases

PATIENT CHARACTERISTICS: Age: Not specified Performance status: Zubrod 0-1 Life expectancy:
Not specified Hematopoietic: Absolute granulocyte count at least 1,500/mm3 Platelet count
at least 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 times upper limit of normal
(ULN) SGOT or SGPT no greater than 2.5 times ULN Renal: Creatinine no greater than 2.0
mg/dL Other: Ability to swallow and/or receive enteral medications via gastrostomy feeding
tube No intractable nausea or vomiting No other prior malignancy within the past 5 years
except adequately treated basal or squamous cell skin cancer, carcinoma in situ of the
cervix, or stage I or II cancer in remission Not pregnant or nursing Fertile patients must
use effective contraception

PRIOR CONCURRENT THERAPY: Biologic therapy: No prior or concurrent immunotherapy
Chemotherapy: No prior chemotherapy No prior adjuvant or neoadjuvant chemoradiotherapy,
including for advanced pancreatic cancer No other concurrent chemotherapy Endocrine
therapy: No prior or concurrent hormonal therapy Radiotherapy: See Chemotherapy No prior
radiotherapy, except for palliation to metastatic sites No concurrent radiotherapy Surgery:
See Disease Characteristics At least 2 weeks since prior surgery for pancreatic cancer and
recovered Prior partial resections of the stomach and duodenum for pancreatic cancer
allowed No prior major resection of the small intestine Prior pancreaticduodenectomy for
pancreatic cancer allowed Other: No concurrent proton pump inhibitors (e.g., omeprazole)
Concurrent antacids or H2 blockers allowed No other concurrent therapy for pancreatic
cancer