Pilot Study of Concomitant NovoTTF-200A and Temozolomide Chemoradiation for Newly Diagnosed Glioblastoma
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
研究概览
简要总结
This study is a prospective single arm trial designed to study the safety, feasibility and preliminary efficacy of a medical device, NovoTTF-200A used concomitantly with standard adjuvant treatment for newly diagnosed glioblastoma.
详细描述
A prospective, single arm, non-randomized, open label pilot trial will enroll ten patients with histologically-confirmed newly diagnosed GBM who meet all eligibility criteria. Patients will be recruited to the study by the principal investigator (PI) or one of the co-investigators (CI) at one institution, Hackensack University Medical Center. Accrual is expected to continue for 18 months.
The protocol has a planned enrollment of 10 patients. Should patients discontinue treatment on protocol for reasons unrelated to toxicity (e.g. lost to follow-up, withdrawal of consent), additional patient (s) may be enrolled to complete enrollment.
Following maximal debulking surgery, patients will undergo a gadolinium enhanced brain MRI within 72 hours and a screening visit 2 to 4 weeks following surgery. Extent of resection will be recorded as biopsy, partial resection or gross-total resection based upon residual enhancing tumor on post-operative MRI.The day prior to XRT start, patients will have a clinic visit for training and application of the NovoTTF-200A device. During this visit, the patient will be educated regarding general use and maintenance of the device, with a particular focus upon strategies to prevent, identify and manage dermatologic adverse events (dAE). Temozolomide will be dosed nightly during XRT as per standard of care, and NovoTTF-200A will be worn continuously, removed during XRT and replaced as soon as possible thereafter.
During XRT and for 12 weeks to follow, the patient will have study visits at regular intervals (TAB A) for a physical examination and to assess toxicity and device compliance. Visits outlined in TAB A are in addition to weekly visits during radiotherapy with the treating radiation oncologist. MRI will be obtained at 4 weeks (+/-7 days) and 12 weeks (+/-7 days) following completion of XRT, and maintenance temozolomide will recommence in 5/28 day cycles as per standard of care. Objective response will be assessed as defined by the Response Assessment in Neuro-Oncology (RANO) criteria (TAB C) by the treating physician and confirmed by a second investigator.
In the case of suspected pseudoprogression, continued treatment and subsequent evaluations will help clarify whether it is true progression. Patients may continue treatment at the discretion of the investigator. If subsequent evaluations suggest that the tumor has in fact progressed, the date of progression will reflex to the date when the issue was first raised. However, if subsequent evaluations demonstrate improvement without change in therapy, the initial tumor increase may be considered pseudoprogression and response may be recorded as not evaluable for that time point. In the case of clinical progression, an unscheduled MRI will be obtained within 1 week of the investigator becoming aware of the clinical progression. No additional MRIs will be required after progression.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed GBM using WHO criteria.
- •Age ≥ 18 years
- •Maximal debulking surgery (at the discretion of the investigator). Biopsy alone is not exclusionary.
- •Life expectancy of at least 3 months.
- •Sexually active participants must agree to the strict use of barrier contraception.
- •Patients must be able to understand the investigational nature of the study and provide informed consent.
- •Adequate hematologic function:
- •Absolute neutrophil count (ANC) ≥ 1.5 x 109/L
- •Platelet count ) ≥ 100 x 109/L
- •Hemoglobin ≥ 10 g /dL
- •Adequate liver function
- •Total bilirubin ≤ 1.5 x ULN
- •AST and ALT ≤ 2.5 x ULN
- •Adequate renal function
- •a. Creatinine ≤ 1.25 x ULN
- •International normalized ratio (INR) or PT and activated partial thromboplastin time (aPTT): 1.5 x ULN (except for subjects receiving anticoagulation therapy). Use of anticoagulants is permitted as long as the INR or aPTT are within therapeutic limits (according to the medical standard of the institution).
排除标准
- •Active participation in another clinical treatment trial. Concomitant protocols for data or tissue collection without intervention are permitted.
- •Any prior treatment for GBM aside from surgery, including carmustine wafers.
- •Women who are pregnant or nursing.
- •Severe acute or chronic medical or psychiatric condition or laboratory abnormality that could increase the risk associated with trial participation, NovoTTF-200A device use or interfere with interpretation of trial results and, in the judgment of the investigator, would make the patient inappropriate for entry into the trial. This includes but not limited to:
- •Patients with inadequately healed surgical incisions or other dermatologic scalp toxicity at baseline (grade 2 or higher, as defined in Section VIII) upon which transducer leads may require placement.
- •Known HIV or other immunosuppressive disease, chronic hepatitis B or hepatitis C
- •Dementia or significantly altered mental status that would prohibit the understanding or rendering of informed consent and compliance with the requirements of the protocol.
- •Implanted pacemaker, programmable shunt, cardiac defibrillator, deep brain stimulator, other implanted electronic devices in the brain or documented clinically significant arrhythmias.
- •Infratentorial glioblastoma.
- •Past hypersensitivity reaction to temozolomide or DTIC.
- •Psychiatric illness that compromises the informed consent process, at the discretion of the investigator.
- •Inability or unwillingness to return for required visits.
- •Previous cytotoxic therapy within the last 5 years.
- •Inability to begin temozolomide concomitant to radiation therapy, for reasons 4 or 7 above.
研究组 & 干预措施
NovoTTF-200A + Temozolomide Chemoradiation
NovoTTF-200A, concomitant with radiotherapy and temozolomide, as front-line therapy for glioblastoma
干预措施: NovoTTF-200A (Device)
NovoTTF-200A + Temozolomide Chemoradiation
NovoTTF-200A, concomitant with radiotherapy and temozolomide, as front-line therapy for glioblastoma
干预措施: Temozolomide (Drug)
NovoTTF-200A + Temozolomide Chemoradiation
NovoTTF-200A, concomitant with radiotherapy and temozolomide, as front-line therapy for glioblastoma
干预措施: 3D conformal or intensity modulated radiation therapy (IMRT) (Radiation)
结局指标
主要结局
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
时间窗: 24 months
Safety and tolerability of combined modality treatment with radiotherapy, temozolomide and NovoTTF-200A based upon the incidence and severity of adverse events.
次要结局
- Overall survival time(From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 120 months)
- Progression free survival at 6 months(From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months)
- Quality of life assessed using the European Organization for Research and Treatment of Cancer (EORTC) Quality of life questionnaire (QLQ-C30)(24 months)
- Quality of life assessed using a European Organization for Research and Treatment of Cancer (EORTC) Brain Cancer questionnaire (BN20)(24 months)