Double-blind, Placebo-controlled, Randomized Phase II-study Investigating the Efficacy of Bevacizumab for Symptom Control in Patients With Malignant Ascites Due to Advanced-stage Gastrointestinal Cancers
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 53
- 试验地点
- 26
- 主要终点
- paracentesis-free survival (ParFS)
研究概览
简要总结
Malignant ascites represents a severe clinical problem for physicians and patients being confronted with this common symptom of advanced-stage gastrointestinal cancer. Unfortunately, there is no standardized and evidence-based treatment for malignant ascites and therapies which are commonly being used are only temporarily effective. Newer modes of therapy, such as the application of the tri-functional antibody catumaxomab, are associated with significant side effects and are limited to patients in stages of good overall performance. Therefore, there is still an urgent need for more effective, longer-lasting, and less toxic modes of treatment for peritoneal effusions caused by gastrointestinal cancers.
Preclinical data strongly suggest that bevacizumab might be a very effective agent for the treatment of malignant ascites, which is in large part caused by the hyperpermeability-promoting factor VEGF. Emerging clinical results from cancer patients with malignant ascites treated with bevacizumab add further support to this idea. Bevacizumab has been tested in a variety of large clinical trials, has a good toxicity profile, and is effective in a number of human cancers underlying malignant ascites.
In the present study, Bevacizumab will be administered as an intraperitoneal infusion at an absolute standardized dosage of 400 mg. This dosage was chosen because it is comparable to the approved standard dosage for intravenous administration which was also used in both studies reporting the successful and safe intraperitoneal administration of Bevacizumab to patients with malignant ascites. Finally, a standardized dosage seems more practical in the particular patient population treated in this study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age >= 18 years
- •Written informed consent has been obtained prior to inclu¬sion into the study
- •Patient is capable and willing to comply with the study
- •Histologically confirmed esophageal, gastric, pancreatic, cholangiocellular, hepatocellular, or colorectal carcinoma
- •Cytologically confirmed ascites OR diagnosis of an exsudate (total protein in ascites > 30 g/l) clinically suggestive for malignant ascites OR morphological diagnosis of peritoneal carcinosis by CT , MRT or ultrasound
- •Ascites clinically judged as not responsive to conventional systemic therapies for primary malignancy
- •Ascites clinically judged as not responsive to diuretics
- •At the time of inclusion paracentesis required at least twice within past 4 weeks.
- •Before inclusion of the patient into the study, a 4-week screening period will allow for a stringent evaluation of the patient regarding fulfillment of inclusion and exclusion criteria. Importantly, no treatments for malignant ascites other than paracentesis and diuretics are allowed during the 4-week screening period.
- •ECOG performance score 0-3
- •Life expectancy > 12 weeks
- •Laboratory parameters:
- •Neutrophils > 1,500/µl
- •Platelets > 100,000/µl
- •Hemoglobin >= 9 g/dl or 5.59 mmol/l Hemastasiology
- •INR <= 1.5 x ULN and aPTT <= 1.5 x ULN within past 7 dClinical chemistry
- •Creatinine clearance > 30 ml/min, serum creatinine < 2.5 x ULN
- •Serum bilirubin < 3.0 x ULN
- •Alkaline phosphatase and transaminases < 3.0 x ULN (in case of liver metastases < 7 x ULN)
- •Urinalysis:
- •Patients with < 2+ proteinuria on dipstick urinalysis.
- •Patients with >= 2+ proteinuria on dipstick urinalysis, who demonstrate < 2.0 g of protein/24 h on 24-h urine collection
排除标准
- •Concomitant malignancies other than gastrointestinal cancers (Patients with curatively treated basal and squamous cell carcino¬ma of the skin and / or in-situ carci¬noma of the cervix are eli¬gible).
- •Bacterial peritonitis as indicated by laboratory results (neutrophil count > 250 / µl ascites) or clinical suspicion
- •Hemorrhagic ascites (ascites hematocrit > 2%)
- •Transudative ascites (total protein in ascites < 30 g/l)
- •Parallel treatment with anti-tumor agents other than the study medication from inclusion into the study until safety follow-up. Chemotherapy may be continued if started before screening phase (- 4 weeks before inclusion). Parallel Treatment with Bevacizumab i.v. is not allowed.
- •Therapy naïve patients
- •Parallel treatment of ascites with measures other than para¬centesis, diuretics, and the study drugs from 4 weeks before inclusion into the study until safety follow-up.
- •Patients with extensive metastases of the liver making up > 70% of the total liver mass
- •Child C cirrhosis of the liver
- •Occlusion or thrombosis of the portal vein.
- •Evidence of current and symptomatic central nervous system (CNS) metas¬ta¬ses or spinal cord compression.
- •Clinically significant cardiovascular diseases, e.g., un¬con¬trolled hypertension, uncontrolled arrhythmia, hemoptoe, cardiovascular accident within the last 6 months before treatment start, unstable angina, congestive heart failure (CHF) NYHA grade III/IV, symptomatic coronary heart disease, peripheral arterial disease stage >= II.
- •History of fistula formation involving an internal organ (e.g. tracheo-oesophagal, bronchopleural, biliary, vagina and bladder)
- •Major surgical procedure, open biopsy, or significant trau¬matic injury within 28 days prior to study treatment start, or anticipation of the need for major surgical procedure during the course of the study.
- •Concomitant treatment with intravenous Bevacizumab for primary malignancy from inclusion into study until safety follow-up. Prior treatment with Bevacizumab for primary malignancy is not exclusionary.
- •Serious non-healing wound, ulcer or bone fracture.
- •Radiotherapy for purposes other than local control of symp¬toms.
- •Evidence of bleeding diathesis or coagulopathy.
- •Hematopoietic diseases.
- •Known intra-abdominal inflammatory process or serious gastrointestinal ulceration.
- •History of chronic intestinal diseases associated with severe diarrhea.
- •Thrombo-embolic events or severe hemorrhage (<= 6 months before treatment start).
- •Known hypersensitivity to the test drug Bevacizumab
- •Evidence of any other disease, metabolic dysfunction, physi¬cal examination finding, or laboratory finding giving reasonable suspicion of a disease or condition that contra-indicates the use of an investigational drug or puts the patient at high risk for treatment-related compli¬cations.
- •With the only exception of full dose (INR > 1.5) oral coumarin-derived anticoagulants, the use of full dose anticoagulants is allowed as long as the INR or a PTT is within therapeutic limits (according to the medical standard in the institution) and the patient has been on a stable dose for at least two weeks at the time of randomisation.
- •Patients who participated within the last 30 days prior to enrolment in a clinical trial and received a non approved investigational drug (e.g. follow up within the trial is not exclusionary).
- •Patients who have participated in this study before.
- •Women, lactating, pregnant or of childbearing potential and fertile men not using a highly effective contraceptive method . [Women of childbearing potential must have a negative pregnancy test (serum ß HCG) within 7 days before the first dose of study drug].
- •Patients who are committed to an institution by virtue of an order issued either by the judicial or the administra¬tive authorities (according to § 40 (1) 4 AMG).
- •Patients who are underage or patients who are incapable to understand the aim, importance and consequences of the study and to give legal informed consent (according to § 40 (4) and § 41 (2) and (3) AMG).
- •Patients with a history of a psychological illness or con¬di¬tion such as to interfere with the patient's ability to un¬der¬stand the requirements of the study.
- •Patients who possibly are dependent on the sponsor or investigator.
研究组 & 干预措施
Arm A Bevacizumab
48 patients randomized into arm A will receive repeated intra¬peritoneal application of Bevacizumab
干预措施: Bevacizumab (Drug)
Arm B Placebo
26 patients randomized into arm B will receive repeated intra¬peritoneal application of Placebo
干预措施: Placebo (Other)
结局指标
主要结局
paracentesis-free survival (ParFS)
时间窗: one year
The first primary endpoint will consist of paracentesis-free survival (ParFS) which will be calculated as the time period between the initial puncture after randomization to the first subsequent paracentesis or other symptomatic treatments for ascites with the exception of diuretics or until death (whichever occurs first)
次要结局
- All adverse events(12 weeks)
- Best Response (BR)(12 weeks from 1st application)
- Volume of ascites(12 weeks)
- Quality of life(12 weeks)
- Changes in ECOG performance status(baseline and 12 weeks)
- Pharmacokinetics of Bevacizumab and VEGF concentrations(12 weeks)
- Proportions of patients with adverse events grades 3, 4, or 5.(12 weeks)
- Proportions of patients with adverse events of special interest(12 weeks)
- Changes in laboratory values and vital signs.(baseline, every two weeks up to week 12)