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临床试验/NCT02041845
NCT02041845进行中(未招募)不适用

A Randomized Phase II Study Comparing Two Schedules of Hyperfractionated Thoracic Radiotherapy in Limited Disease Small Cell Lung Cancer

Norwegian University of Science and Technology22 个研究点 分布在 3 个国家目标入组 177 人开始时间: 2014年7月8日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
177
试验地点
22
主要终点
survival

研究概览

简要总结

The majority of patients with limited disease small cell lung cancer (SCLC) experience recurrent disease despite receiving concurrent chemoradiotherapy. New agents and dose-escalation of chemotherapy have not provided a survival benefit. Local failure accounts for high proportion of recurrences. Improved thoracic radiotherapy (TRT) might increase local control and thus reduce the recurrence rate and prolong survival. Positron emission tomography (PET CT) is better for staging of SCLC than computer tomography (CT) and bone scan. More precise localization of tumors leads to more accurate definition of target volumes for TRT and reduce the radiation dose to normal tissue. A large proportion of patients relapse and die within one and two year after therapy. Few patients survive longer than three years. Thus, two-year survival is considered a clinically highly relevant measure of efficacy.

The aim of this study is to compare two schedules of TRT with respect to local control, progression free survival, overall survival, toxicity and health-related quality of life. In addition patients who have the best outcomes and tolerate chemoradiotherapy will be characterized (e.g. clinical characteristics, blood biomarkers, body composition).

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
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

入选标准

  • Histologically or cytologically confirmed small-cell lung cancer (SCLC)
  • Limited disease (stage II-III)
  • Stage I if ineligible for surgery
  • Eastern Cooperative Oncology Group (ECOG) Performance 0-2
  • Measureable disease according to the Response Evaluation Criteria In Solid Tumors (RECIST) 1.1
  • Adequate organ function defined as: (a) Serum serum alanine transaminase (ALT) ≤ 3 x upper limit of normal (ULN); (b) Total serum bilirubin ≤ 1.5 x ULN; (c) Absolute neutrophil count (ANC) ≥ 1.5 x 109/L; (d) Platelets ≥ 100 x 109/L; (e) Creatinine < 100 µmol/L and calculated creatinine-clearance > 50 ml/min. If calculated creatinine-clearance is < 50 ml/min, an ethylene diamine tetra-acetic acid (EDTA) clearance should be performed.
  • Pulmonary function: Forced Expiratory Volume in One Second (FEV1) > 1 l or 30 % of predicted value and diffusing capacity of the lungs for carbon monoxide (DLCO) > 30 % of predicted value
  • All fertile patients should use safe contraception
  • Written informed consent

排除标准

  • prior systemic therapy for small-cell lung cancer
  • Previous radiotherapy to the thorax
  • malignant cells in pericardial or pleural fluid (at least one sample should be analysed if pleural fluid is present
  • serious concomitant systemic disorders (for example active infection, unstable cardiovascular disease) that in the opinion of the investigator would compromise the patient's ability to complete the study or interfere with the evaluation of the efficacy and safety of the study treatment
  • conditions - medical, social, psychological - which could prevent adequate information and follow-up
  • clinically active cancer other than SCLC. Hormonal therapy for prostate cancer or breast cancer and basocellular carcinoma of the skin is allowed
  • pregnancy, lactation

结局指标

主要结局

survival

时间窗: 2 years

measured for all patients from the date of the first day of the first course of chemotherapy until the date of death from any cause (or last contact/observation if lost to follow-up - or the follow-up is completed before all patients die).

次要结局

  • health related quality of life (HRQoL)(From baseline, before and after radiotherapy and then at follow-up every 3 months until 24 months after start of chemotherapy. Then every 6 months until 5 year after start of therapy)
  • progression free survival (PFS)(2 years)
  • overall survival(3 years)
  • toxicity(2 years)
  • Local control(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (22)

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