EUCTR2019-003058-10-SK进行中(未招募)1 期
Prospective, multicentre phase II study of de-escalation of primary chemoradiotherapy of squamous cell carcinoma of oropharynx (OPC) associated with human papilloma virus (HPV) - NaDeJ
VÝCHODOSLOVENSKÝ ONKOLOGICKÝ ÚSTAV, a.s.0 个研究点目标入组 120 人开始时间: 2019年9月16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
- 120
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
- •Oropharyngeal squamous cell carcinoma
- •Positivity of p16 by imunohistochemistry
- •Clinical stage T1-T2, N1-N2c or T3, N2-N2c, UICC 8th edition without distant metastases
- •The lifetime cumulative history of smoking cannot exceed 20 packages / years
- •WHO status 0-1
- •Age = 18 years
- •Both genders
- •Hemoglobin = 10 g/l
- •Platelets =1 00x 10x9/l
- •Neutrophils = 1,5 x 10x9/l
- •Adequate renal functions enable one-week therapy of cisplatina
- •Bilirubin, AST or ALT 3x upper limit of norm
- •Negative pregnancy test
- •Signed informed consent
- •Slovak language
- •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 120
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Tumor in the oral cavity or in nasopharynx or in the hypopharynx or larynx if the p16 is also positive
- •Tumor of unknown origin (p16 positivity too)
- •Simultaneous tumors
- •Patients with invasive malignancy (except non-melanoma skin cancer) and a history of tumor diagnosis less than 3 years
- •Previous radiotherapy in the head and neck area to overlap the irradiated volume
- •Unstable angina or congestive heart failure requiring hospitalization for the last 6 months
- •Transmural myocardial infarction last 6 months
- •Active infection requiring i.v. antibiotics at the time of registration
- •Chronic obstructive bronchoplumonal disease with exacerbation or other respiratory disease requiring hospitalization or postponement of study treatment within 30 days of enrollment
- •Hepatic insufficiency with clinical jaundice and impaired coagulation
- •Active AIDS disease, but the protocol does not require HIV testing
- •Previous allergic reaction to cisplatin
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