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临床试验/NCT04830826
NCT04830826已完成不适用

A Prospective, National, Multi-center, Non-intervention Real-world Study of Adjuvant Therapy in Early Stage NSCLC With EGFR Mutation-Positive in China

The First Affiliated Hospital of Guangzhou Medical University51 个研究点 分布在 1 个国家目标入组 1,490 人开始时间: 2020年7月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,490
试验地点
51
主要终点
The distribution of participants with initial adjuvant treatment pattern after radical resection surgery for early-stage NSCLC patients

研究概览

简要总结

This study is a prospective, national, multi-center, non-interventional study. The main purpose is to explore the initial adjuvant treatment pattern after radical resection for early-stage NSCLC patients with EGFR Mutation-Positive in the real world. The secondary purpose was to observe the postoperative follow-up treatment pattern and its subgroups (based on different EGFR mutation status and different clinical stages).

详细描述

About 2,000 eNSCLC patients who received radical resection from about 50 research centers across the country will be included in this study, and will be followed up to 2 years after enrollment according to the actual clinical situation. The analysis method of this study is mainly based on descriptive statistics. The information about the human genetic resources of the subjects to be collected includes: demography, physical examination, WHO fitness status, medical history, smoking history, disease characteristics, surgical information, initial and follow-up adjuvant treatment pattern, laboratory tests, survival status, and adverse events related to gefitinib/osimertinib, serious adverse events/non-severe ADR, measures taken for adverse events, outcome of adverse events.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Informed consent signed;
  • Newly confirmed EGFR Mutation-Positive NSCLC confirmed by histopathology except for cytology;
  • Receiving or not receiving neoadjuvant treatment before surgery;
  • Patients with stage I-III NSCLC undergo confirmed radical R0 resection;

排除标准

  • Patients who currently or have previously participated in any other anti-tumor clinical studies;
  • Patients with NSCLC who have received any systemic anti-cancer therapy as the main treatment in the past. Cytotoxic therapy, targeted therapy (tyrosine kinase inhibitors or monoclonal antibodies) and immunotherapy included except for the use of neoadjuvant therapy;
  • Patients who have received adjuvant therapy before enrollment.
  • Patients with stage I-III NSCLC whose surgical resection cannot be confirmed.
  • Patients assessed by the investigator as unfit for enrollment, such as neurological disorders or metabolic disorders, physical examination or laboratory examination suspected that the patient has a possible disease, or has contraindications to the use of study drugs, or has treatment-related complications High risk etc.

结局指标

主要结局

The distribution of participants with initial adjuvant treatment pattern after radical resection surgery for early-stage NSCLC patients

时间窗: 2 years

Descriptive summary statistics ( total number of cases, number of missing cases, frequency, and percentage of each category) were used to describe the distribution of participants with initial adjuvant treatment patterns, including chemical, targeted, combined, or other therapy. Set subgroup analysis for different initial adjuvant treatment pattern, including different clinical stages (according to phase I/ Phase II/ stage III) and different EGFR mutation status (19del or 21 L858R);

The interval from the date of operation to the start date of initial adjuvant therapy with EGFR-TKI.

时间窗: 2 years

Calculate the interval of operation to the adjuvant therapy with EGFR-TKI, which is classified into single-drug therapy and combined therapy. The total number of cases, number of missing cases, mean, standard deviation, median, 25th and 75th percentiles, minimum and maximum were used for statistical description.

Numbers of therapy cycles of initial adjuvant treatment

时间窗: 2 years

The patients with chemotherapy were mainly calculated, divided into chemotherapy and targeted combination chemotherapy. The total number of chemotherapy cycles, the number of missing cases, the mean, standard deviation, the median, the 25th and 75th percentiles, the minimum and the maximum were statistically described

Time on initial adjuvant treatment

时间窗: 2 years

Calculate the time from the start date to the end of initial adjuvant treatment. The total number of cases, number of missing cases, mean, standard deviation, median, 25th and 75th percentiles, minimum and maximum were used for statistical description.

次要结局

  • Numbers of therapy cycles of follow-up treatment(2 years)
  • The distribution of participants with follow-up treatment pattern after initial adjuvant treatment.(2 years)
  • The interval from the date of operation to the start date of the follow-up treatment with EGFR-TKI.(2 years)
  • Time on follow-up treatment(2 years)

研究者

发起方
The First Affiliated Hospital of Guangzhou Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jianxing He

Clinical Professor

The First Affiliated Hospital of Guangzhou Medical University

研究点 (51)

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