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临床试验/NCT05557474
NCT05557474招募中不适用

Development and Clinical Validation of Early-stage Lung Cancer Prognostic Kit and Immunotherapy Companion Diagnostic Laboratory Developed Tests

Chung Shan Medical University2 个研究点 分布在 1 个国家目标入组 236 人开始时间: 2021年10月1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
236
试验地点
2
主要终点
disease free survival

研究概览

简要总结

Lung cancer is the leading cause of cancer mortality worldwide in spite of the advanced progresses in medication and low-dose CT screening. The early-stage lung cancer accounts for less than 50% of newly diagnosed lung cancer in Taiwan, even in stage IB patients proximately 30% still suffer from recurrence and metastasis.

The International Cancer Moonshot Project recently established the first comprehensive proteogenomics profiling of early-stage lung cancer patients in East Asia, revealing a proteomics-informed classification to identify a new "late like" subtype, which can identify a subgroup of early-stage patients with worse clinicopathological features (Cell, Cover story, 2020). This study has been featured in prestigious journals (Nat Rev Clin Oncol; Cancer Discov, 2020) and led to two provisional US patents. In this proposal, taking the discovery from the Cancer Moonshot multiomics database, the investigators aim to translate these findings into clinical utilities. Two subprojects are proposed. (1) Validation of "late-like" protein markers for identifying high-risk early-stage lung cancer: Two IVD kits will be developed, including high-risk early-stage lung cancer IHC prediction kit for tumor staining and high-risk early lung cancer ELISA prediction kit for noninvasive diagnosis. (2) Conducting a prospective clinical trial to evaluate the accuracy of high-risk early-stage lung cancer IHC prediction kit and high-risk early-stage lung cancer ELISA prediction kit.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Willing to sign and provide subject consent.
  • Male or female of age 20 or older.
  • Patients diagnosed with lung adenocarcinoma by tumor pathology.
  • Lung cancer with the pathological stage of IA/IB/II/IIIA according to the American Joint Committee on Cancer Staging Manual (8th Edition).
  • Complete tumor resection (R0 resection).
  • The East Coast Cancer Clinical Research Collaborative (ECOG) performance status was 0 or 1 at the time of grouping.
  • Those willing to provide tumor tissue or cytology specimens (including surgical specimens, tissue biopsy specimens, or cytology specimens), blood and body fluid specimens (for follow-up or disease recurrence, such as urine, malignant pleural effusion, ascites, pericardial fluid, etc.).

排除标准

  • Not primary lung cancer patients.
  • Lung cancer patients whose pathological stage is not IA/IB/II/IIIA according to the American Joint Committee on Cancer Staging Manual (8th Edition) after surgery.
  • Patients with uncontrolled malignant tumors other than lung cancer.
  • Uncontrolled systemic disease (such as diabetes, hypertension, active infection, etc.) (determined by the principal investigator )
  • Pregnant women.
  • Any condition may put the patient at serious risk, may affect the interpretation of the trial results, or may seriously interfere with the patient's participation in the trial.

研究组 & 干预措施

Lung cancer post surgery recurrence follow up

Lung adenocarcinoma, stage IA/IB/II/IIIA post-surgery follow up

干预措施: Early-stage lung cancer prognostic kit -- ELISA (Other)

Lung cancer post surgery recurrence follow up

Lung adenocarcinoma, stage IA/IB/II/IIIA post-surgery follow up

干预措施: Early-stage lung cancer prognostic kit -- IHC (Other)

结局指标

主要结局

disease free survival

时间窗: 5 years

Disease free survival

次要结局

  • Overall survival(10 years)

研究者

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

Gee-Chen Chang

Chung Shan Medical University

Chung Shan Medical University

研究点 (2)

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