EUCTR2007-003098-21-IT进行中(未招募)不适用
INTEGRATED PROTOCOL OF CHEMO-RADIOTHERAPY IN THE TREATMENT OF THE OLD PATIENTS WITH NSCLC STAGE III. PHASE II TRIAL - ND
AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO0 个研究点开始时间: 2007年7月20日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •Hystological or cytological diagnosis of NSCLC;
- •Stage IIIA and IIIB (excluded the N3 sovraclavear and/or T4 for positive pleural cytology);
- •ECOG Performance Status 0-1;
- •Age >= 70 years;
- •Not previous chemotherapy;
- •Life expectancy of at least 12 weeks;
- •PFR (FEV1>45%; DLCO>45% of the theoretical value)
- •Adeguate bone marrow reserve: granulocytes >= 1500; platelets >= 100.000; hemoglobin >=10 gr/dl; ?
- •Normal renal function (creatinin <= 1,5 mg/dl) and hepatic (total bilirubin <= 2,0 mg/dl and levels of AST/ALT within five times the normal value);
- •Absence of significative hepatic, cardiac pathology and of comorbidity that may be interfere with the therapy, the controls and the follow up;
- •Informed Consent written
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Active or uncontrolled infections
- •Hystory present or past of allergy
- •Significant cardiovascular pathology
- •Uncontrolled Diabetes Mellitus
- •Weight dicrease >10%
- •Second tumor within previous 5 years (except carcinoma in situ of the portio, cutaneous carcinoma, superficial carcinoma of the blister with radical treatment)
- •Impossibility to perform a follow-up quickly if a significant toxicity is present
研究者
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