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临床试验/NCT05889247
NCT05889247招募中不适用

Circulating Tumor DNA Guided Treatment Monitoring in Advanced Lung Cancer - a Randomized Interventional Study

Zealand University Hospital5 个研究点 分布在 1 个国家目标入组 350 人开始时间: 2023年7月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
350
试验地点
5
主要终点
Overall Survival

研究概览

简要总结

The study is a prospective randomized interventional study including patients with advanced non-small cell lung cancer, receiving immunotherapy, with the aim of optimizing treatment monitoring. The study aims to investigate the clinical utility of liquid biopsy monitoring in order to reduce the numbers of inefficient treatments and needless toxicity - and to explore the cost-effectiveness and cost-utility of introducing liquid biopsy monitoring in daily clinical practice.

详细描述

Lung cancer is the leading cause of cancer-related death worldwide with Non-Small Cell Lung Cancer (NSCLC) being the most common subtype. Performance status deterioration due to progressive symptoms and toxicity by treatments are major challenges in managing advanced NSCLC patients. Moreover, standard treatment monitoring by radiologic scans is often imprecise. This technology has limited sensitivity as only a visible increase or decrease in tumor mass can be evaluated, making interpretation challenging and conclusions of whether patients benefit from treatment indefinite. Interpretation of radiologic scans has been further challenged after implementation of immunotherapy, causing immunotherapy-induced recruitment of immune cells resembling increment in tumor size, called "pseudo-progression." More sensitive methods are highly needed to reduce ineffective treatments and needless toxicity. Liquid biopsy has the potential to overcome these challenges by measuring molecular changes with high precision in a dynamic manner. Recent studies have demonstrated its promising potential as a biomarker predictive of treatment efficacy and overall survival. In a recent real-life study, investigators found that ctDNA measurements could reduce 33% of likely inefficient treatments and clarify 79% of non-conclusive CT-scans, highlighting the clinical potential. A randomized interventional multicenter study will be performed, investigating the true clinical potenial of liquid biopsy compared to standard monitoring by radiological scans. A total of 350 patients with advanced NSCLC will be included in the study from three Departments of Clinical Oncology. In the interventional arm, liquid biopsy monitoring will be the basis for treatment discontinuation before the standard two years of immunotherapy in patients reaching a complete molecular response in plasma. Thus clarifying the question if treatment duration can be reduced for the benefit of patients and health cost.

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
Single (Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Newly diagnosed, histologically verified, Non-Small Cell Lung Cancer (NSCLC)
  • Advanced or locally advanced disease without curative intended treatment options
  • Age > 18 years
  • Eastern Cooperative Oncology Group (ECOG) score of Performance Status (PS) 0-1
  • Measurable disease according to the iRECIST criteria version 1.
  • Eligible to first line immunotherapy (monotherapy)
  • Signed informed consent

排除标准

  • Targetable alterations in EGFR, ALK or ROS-1
  • Other active cancers

研究组 & 干预措施

ctDNA monitoring

Experimental

Treatment monitoring by longitudinal circulating tumor DNA measurements and Quality of Life assessments

干预措施: Circulating tumor DNA treatment monitoring (Other)

CT scan monitoring

No Intervention

Treatment monitoring by longitudinal CT scans (standard) and Quality of Life Assessments

结局指标

主要结局

Overall Survival

时间窗: through study completion, an average of 3 years

Overall Survival

次要结局

  • Common Terminology Criteria for Adverse Events(through study completion, an average of 3 years)
  • Health Cost/Utility(From randomization to first detection of progressive disease, an average of 3 years)
  • Physicians Global Assessment to measure quality of life(through study completion, an average of 3 years)
  • Number of Treatments(From randomization to first detection of progressive disease, an average of 3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Malene Støchel Frank

Medical Oncologist, PhD

Zealand University Hospital

研究点 (5)

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