RO4929097 Before Surgery in Treating Patients With Pancreatic Cancer

• Status: Terminated
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

This phase I trial is studying the side effects of RO4929097 before surgery in treating patients with pancreatic cancer. RO4929097 may stop the growth of tumor cells by blocking some enzymes needed for cell growth. Giving RO4929097 before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Cancer Institute (NCI)
• Treatments: R04929097

Criteria

Inclusion Criteria:

• Histologically or cytologically confirmed pancreatic adenocarcinoma

• T1-3, N0-1, and M0 disease

• Surgically resectable disease confirmed by a surgeon experienced in pancreatic surgery

• No borderline resectable disease defined as any of the following:

• Tumors with severe unilateral or bilateral SMV/portal involvement impingement

• Abutment (or) encasement of hepatic artery

• SMA or celiac encasement (or) presence of SMV occlusion by tumor

• No metastatic disease

• ECOG performance status 0-1

• Life expectancy > 6 months

• WBC ≥ 3,000/mm³

• ANC ≥ 1,500/mm³

• Platelet count ≥ 100,000/mm³

• Hemoglobin ≥ 9 g/dL

• Total bilirubin ≤ 2 mg/dL

• AST and ALT ≤ 2.5 times upper limit of normal

• Creatinine ≤ 2 mg/dL

• Calcium, magnesium, phosphorous, and potassium normal

• Negative pregnancy test

• Not pregnant or nursing

• Fertile patients must use effective barrier-method contraception 4 weeks before, during, and for ≥ 12 months after completion of treatment

• Able to swallow tablets

• No malabsorption syndrome or other condition that would interfere with intestinal absorption

• No history of allergic reactions attributed to compounds of similar chemical or biologic composition to gamma-secretase inhibitor RO4929097 or other agents used in the study

• No uncontrolled hypocalcemia, hypomagnesemia, hyponatremia, hypophosphatemia, or hypokalemia despite adequate electrolyte supplementation

• Grade 1 hyponatremia with sodium ≤ 131 mg/dL is permissible

• No uncontrolled intercurrent illness including, but not limited to, any of the following:

• Ongoing or active infection

• Symptomatic congestive heart failure

• Unstable angina pectoris

• Cardiac arrhythmia other than chronic

• Stable atrial fibrillation

• Psychiatric illness/social situations that would limit compliance with study requirements

• No baseline QTcF > 450 msec (male) or QTcF > 470 msec (female)

• Patients with a prior cancer with evidence of active cancer are excluded from this study

• Patients with a prior cancer are permitted to enter this study as long as there is no documented evidence of active malignancy

• No uncontrolled electrolyte abnormalities including hypocalcemia, hypomagnesemia, and hypokalemia

• No symptomatic congestive heart failure, unstable angina pectoris, and a history of torsades de pointes or other significant cardiac arrhythmias

• No requirement for antiarrhythmics or other medications known to prolong QTc

• No other concurrent anticancer agents or therapies

• Recovered to < grade 2 toxicity related to prior therapy

• No prior chemotherapy or radiotherapy for pancreatic cancer

• No other concurrent investigational agents

• No concurrent medications with narrow therapeutic indices that are metabolized by cytochrome P450 (CYP450), including warfarin sodium (Coumadin®), ketoconazole, or grapefruit juice

• No concurrent strong inducers or inhibitors of CYP3A4

• No concurrent combination antiretroviral therapy for HIV-positive patients