A Randomized, Open-Label, Dose Escalation Study of Bevacizumab With Ambulatory Blood Pressure Monitoring in Previously Untreated Patients With Advanced Non-squamous Non-Small Cell Lung Cancer
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
- 试验地点
- 3
- 主要终点
- Change in 24 Hour Diastolic Blood Pressure (DBP)
研究概览
简要总结
The purpose of this study is to see if higher dose of bevacizumab can be taken safely by some patients and if changes in the dose of bevacizumab have any effect on blood pressure.
详细描述
Carboplatin and pemetrexed are FDA approved chemotherapy agents for patients with advanced non squamous non small cell lung cancer. Bevacizumab is also FDA approved in lung cancer , and the combination of all three drugs is promising. The doctors directing this research want to learn how to better personalize drug dosing of bevacizumab by identifying people who could safely take a higher dose of the drug.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 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 89 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients must have histologically or cytologically confirmed, newly diagnosed Stage IIIB, stage IV, or recurrent non-squamous NSCLC for which they have not received chemotherapy.
- •Patients must have completed radiation therapy 2 weeks prior to enrollment. Patients may have received adjuvant therapy, provided the regimen included no more than one of the study agents.
- •Patients must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension.
- •Age >18 years. •Life expectancy of greater than 4 months.
- •ECOG performance status of 0 or 1
- •Patients must have normal organ and marrow function
- •Patients on anticoagulation are allowed.
- •Women of child-bearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation.
- •Ability to understand and the willingness to sign a written informed consent document.
排除标准
- •Disease-Specific
- •Patients who have had received prior chemotherapy (in the setting of recurrent disease, other than their original adjuvant therapy)
- •Patients may not be receiving any other investigational agents.
- •Patients with histologic evidence of predominantly squamous lung cell cancer
- •General Medical Exclusions
- •Inability to comply with study and/or follow-up procedures
- •Malignancy other than superficial basal cell and superficial squamous of the skin or carcinoma in situ of the cervix within last five years
- •Bevacizumab-Specific Exclusions
- •Inadequately controlled hypertension
- •Prior history of hypertensive crisis or hypertensive encephalopathy
- •New York Heart Association Grade II or greater congestive heart failure
- •History of myocardial infarction or unstable angina within 6 months prior to Day 1
- •History of stroke or transient ischemic attack within 6 months prior to Day 1
- •Known CNS disease, except for treated brain metastasis.
- •Significant vascular disease within 6 months prior to Day 1
- •History of hemoptysis within 1 month prior to Day 1
- •Evidence of bleeding diathesis or significant coagulopathy
- •Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1 or 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 Day 1
- •History of diverticulitis, abdominal fistula or gastrointestinal perforation within 6 months prior to Day 1
- •Serious, non-healing wound, active ulcer, or untreated bone fracture
- •Proteinuria as demonstrated by a UPC ratio 1.0 at screening
- •Known hypersensitivity to any component of bevacizumab
- •Pregnancy (positive pregnancy test) or lactation.
- •Mixed tumors will be categorized by the predominant cell type unless small cell elements are present.
- •Uncontrolled intercurrent illness including, ongoing or active infection or psychiatric illness/social situations that would limit compliance with study requirements.
- •Any unstable condition that in the opinion of the investigator is likely to interfere with collection of accurate blood pressure measurement data .
- •HIV-positive patients on combination antiretroviral therapy.
研究组 & 干预措施
Group B
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin+Pemetrexed+Bevacizumab 15 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Pemetrexed (Drug)
Group B
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin+Pemetrexed+Bevacizumab 15 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Carboplatin (Drug)
Group A
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Pemetrexed (Drug)
Group A
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Carboplatin (Drug)
Group A
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Bevacizumab 7.5 mg/kg (Drug)
Group B
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin+Pemetrexed+Bevacizumab 15 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Bevacizumab 7.5 mg/kg (Drug)
Group B
Carboplatin and Pemetrexed with Bevacizumab 7.5 mg/kg once, followed three weeks later by Carboplatin+Pemetrexed+Bevacizumab 15 mg/kg and bevacizumab every 3 weeks for two doses
干预措施: Bevacizumab 15 mg/kg (Drug)
结局指标
主要结局
Change in 24 Hour Diastolic Blood Pressure (DBP)
时间窗: 2 cycles
The change for each patient was calculated as mean 24 hour DBP during cycle 2 - mean 24 hour DBP during cycle 1
次要结局
- Response Rate(2 years)
- Change in Tumor Size From Baseline(2 years)
- Progression Free Survival(2 years)