EUCTR2017-000498-35-PL进行中（未招募）1 期
Very early FDG-PET-response adapted targeted therapy for advanced Hodgkin lymphoma: a single-arm phase II study - COBRA
European Organisation for Research and Treatment of Cancer (EORTC)0 个研究点目标入组 150 人开始时间: 2019年3月5日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Previously untreated, histologically proven classical Hodgkin lymphoma;
- •Staged by PET with diagnostic-quality CT (i.v. contrast).
- •- Clinical stages according to Lugano 2014 and based on FDG/PET CT:Stage IIB with large mediastinal mass > 1/3 max transverse diameter thorax and/or extranodal lesion(s) (GHSG)
- •- Stage III - IV
- •Participation in translational research is mandatory and therefore patient must consent to additional blood samples at multiple time points in the study. In addition, sufficient tissue must be available (15 blank formalin fixed paraffin embedded tissue samples mounted on APES slides or a tissue block).
- •Age =18 and =60
- •WHO performance status 0-2
- •Patient demonstrates adequate organ function as defined in the protocol.
- •Women of child bearing potential (WOCBP) must have a negative serum pregnancy test within 72 hours prior to the first dose of study treatment.
- •Patients of childbearing / reproductive potential should use two birth control methods, as defined by the investigator, from the time of signing the informed consent form , and throughout the entire study and for 6 months after the last dose of treatment.
- •Female subjects who are breast feeding should discontinue nursing prior to the first dose of study treatment and until 6 months after the last study treatment.
- •Absence of any medical, psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
- •Before patient registration, written informed consent must be given according to ICH/GCP, and national/local regulations.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 150
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Known cerebral or meningeal disease (HL or any other etiology), including signs or symptoms of Progressive Multifocal Leukoencenphalopathy
- •Symptomatic neurologic disease compromising normal activities of daily living or requiring medications
- •Sensory or motor peripheral neuropathy greater than or equal to grade 2 according to CTCAE version 5.0
- •Any of the following cardiovascular conditions or values:
- •- within 6 months before registration:
- •A left-ventricular ejection fraction <50%
- •New York Heart Association (NYHA) Class III or IV heart failure (see Appendix D).
- •Evidence of current uncontrolled cardiovascular conditions, including cardiac arrhythmias, congestive heart failure (CHF), angina, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities
- •symptomatic coronary heart disease (stable angina pectoris is allowed)
- •severe uncontrolled hypertension defined as blood pressure (BP) >150/100 mmHg despite optimal antihypertensive treatment
- •- within 2 years before registration:
- •Myocardial infarction
- •Patients with poorly controlled diabetes mellitus (HbA1c > 7.5 % or a fasting blood sugar > 200 mg/dL).
- •Any active systemic viral, bacterial, or fungal infection requiring systemic antibiotics within 2 weeks prior to registration.
- •Known HIV infection, chronic active hepatitis C, HBV positivity (HBsAg + patients; HBsAg -/HBcAb+/HBV DNA+ patients).
- •Note: HBsAg-/HBV DNA – patients are eligible; patients who are seropositive due to vaccination are eligible
- •Concomitant or previous malignancies within the past 5 years with the exception of adequately treated carcinoma in situ of the cervix , nonmelanoma skin cancer.
- •Previous treatment with anti CD30 antibodies
- •Known hypersensitivity to any excipient contained in Brentuximab Vedotin formulation and other study drugs. Refer to Summary Product Characteristics for list of excipients.
- •Concurrent anti-cancer treatment or use of any investigational agent(s)
研究者
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