Phase II Study of Avastin, Fluorouracil, Doxorubicin and Streptozocin in Locally Advanced and Metastatic Pancreatic Endocrine Tumors

H. Lee Moffitt Cancer Center and Research Institute1 个研究点分布在 1 个国家目标入组 1 人开始时间: 2007年8月最近更新: 2017年3月23日

适应症

干预措施

试验速览

阶段: 2 期
状态: 终止
发起方: H. Lee Moffitt Cancer Center and Research Institute
入组人数: 1
试验地点: 1
主要终点: Number of Participants With Progression Free Survival (PFS) at 12 Months

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Open label, single-arm phase II study of avastin combined with fluorouracil, doxorubicin and streptozocin administered in 28-day cycles. Treatment will continue until progression of disease, or until withdrawal due to toxicity, or up to a maximum of 12 cycles (48 weeks). In order to reduce the risk of cardiac toxicity, doxorubicin will be administered for a maximum of 8 cycles. If disease has not progressed after 12 cycles of treatment, avastin monotherapy will continue until disease progression or withdrawal due to toxicity.

详细描述

Patients will need to come for 24 study visits in all. Most study visits will take about 2 hours. At some of these study visits, the doctor

Will do a physical exam
Will take blood for routine lab tests
Will do a urinalysis
Will administer study medication Some study visits may be longer because patient will have a CT scan or an MRI.

At patient's last visit, they will have a CT scan or MRI.

After treatment starts, patient will:

Have their blood pressure monitored with every dose of Avastin® (about every 2 weeks).
Have a history and physical with every chemotherapy cycle (about every 4 weeks).
Have their blood taken for routine blood tests with every chemotherapy cycle (about every 4 weeks).
Have a CT scan or MRI during every other cycle (about every 8 weeks).
Have a MUGA scan during every 4 cycles (about 16 weeks).
Have blood taken for tumor markers during every cycle only if their markers were high at baseline.
Patients will receive study medication to treat their cancer:
Fluorouracil on days 1 through 5 of each cycle through cycle 12
Doxorubicin on day 1 of each cycle through cycle 8
Streptozocin on days 1 through 5 of each cycle through cycle 12
Avastin® on days 1 and 15 of each cycle through cycle 12

研究设计

研究类型: Interventional
分配方式: Na
干预模型: Single Group
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 80 Years（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Patients must have locally advanced (unresectable) or metastatic, well or moderately differentiated pancreatic endocrine tumors.
•Measurable disease on CT scan or MRI.
•Age ≥ 18 years and ≤ 80 years.
•Use of effective means of contraception (men and women) in subjects of child-bearing potential
•Adequate renal function (serum creatinine ≤1.5, urine protein:creatinine ratio <1.0 or urine dipstick for proteinuria < 2+ (patients discovered to have ≥ 2+ proteinuria on dipstick urinalysis at baseline should undergo a 24 hour urine collection and must demonstrate ≤ 1 g of protein in 24 hours to be eligible).
•Adequate hepatic function (bilirubin ≤2.0, AST and ALT ≤ 3x ULN.
•Adequate hematologic function (WBC ≥ 3,000, ANC ≥ 1500, platelets ≥ 100,000)

排除标准

•Prior therapy with fluorouracil, doxorubicin, streptozocin or avastin
•Ejection fraction on MUGA <50%
•ECOG performance status > 2
•Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an experimental drug study other than a Genentech-sponsored avastin cancer study
•Inadequately controlled hypertension (defined as systolic blood pressure >150 and/or diastolic blood pressure > 100 mmHg on antihypertensive medications)
•Any prior history of hypertensive crisis or hypertensive encephalopathy
•Unstable angina
•New York Heart Association (NYHA) Grade II or greater congestive heart failure
•History of myocardial infarction or unstable angina within 6 months prior to study enrollment
•History of stroke or transient ischemic attack within 6 months prior to study enrollment
•Significant vascular disease (e.g., aortic aneurysm, aortic dissection)
•Symptomatic peripheral vascular disease
•Evidence of bleeding diathesis or coagulopathy
•Presence of central nervous system or brain metastases
•Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0, anticipation of need for major surgical procedure during the course of the study
•Core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to study enrollment
•Pregnant (positive pregnancy test) or lactating. Use of effective means of contraception (men and women) in subjects of child-bearing potential
•Proteinuria at screening as demonstrated by either
•Urine protein: creatinine (UPC) ratio ≥ 1.0 at screening OR
•Urine dipstick for proteinuria ≥ 2+ (patients discovered to have ≥2+ proteinuria on dipstick urinalysis at baseline should undergo a 24 hour urine collection and must demonstrate ≤ 1g of protein in 24 hours to be eligible).
•History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to Day 0
•Evidence of duodenal invasion on CT scan, MRI, or endoscopy
•Known hypersensitivity to any component of avastin
•Serious, non-healing wound, ulcer, or bone fracture
•Inability to comply with study and/or follow-up procedures