跳至主要内容
临床试验/NCT07109154
NCT07109154招募中不适用

DeniLA: Comprehensive Demographics and Clinical Profile of NSCLC Patients: Analyzing Guideline-Concordant Care in First-line Treatment Patterns Observational Study (Prospective and Survey); Evaluation Patterns of Choice in First Line Treatment of Metastatic NSCLC

AstraZeneca7 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2025年11月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
AstraZeneca
入组人数
200
试验地点
7
主要终点
Describe epidemiological characteristics of patients diagnosed with NSCLC in Brazil real-world.

研究概览

简要总结

This is a prospective, observational, multicenter study, in which clinical and demographic data will be extracted from medical records. Convenience sample, with an estimated inclusion of 200 patients treated in seven participating centers.

Eligible tumors for this project will be from patients with advanced (unresectable or metastatic) non-small cell lung carcinoma, who will start first-line oncological treatment in one of the participating centers between 2025 and 2026 (between January 2025 and January 2026). Patients must be over 18 years old and data must be available in electronic medical records.

Medical records will be assessed to confirm patients' eligibility. Patients with localized disease amenable to local treatment, non-epithelial histology, small cell carcinoma and neuroendocrine tumor will not be eligible.

A survey will be designed targeting thoracic and generalist medical oncologists, aiming to understand the factors guiding the choice of first-line treatment regimens and to compare these insights with real-world data. The survey will be directed to Brazil, with an estimated of 200 filled files.

研究设计

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

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Advanced (unresectable or metastatic) non-small cell lung carcinoma
  • •First-line oncological treatment in one of the participating centers between 2025 and 2026 (between January 2025 and January 2026)
  • •> 18 years old
  • •Data available in electronic medical records.

排除标准

  • •Localized disease amenable to local treatment
  • •Non-epithelial histology
  • •Small cell carcinoma
  • •Neuroendocrine tumor
  • •Patients with unresectable NSCLC who underwent treatment with the PACIFIC protocol and are being followed up.

结局指标

主要结局

Describe epidemiological characteristics of patients diagnosed with NSCLC in Brazil real-world.

时间窗: Through study completation, an average of 2 years

Clinical and demographic data will be extracted from medical records (gender, age at diagnosis, self-reported ethnicity, state, institutional profile (public or private), smoking status, lung cancer family history), clinical characteristics such as comorbidities, histology, extent of disease, metastasis location, tumor stage at diagnosis according AJCC eighth edition, ECOG status, frequency of biomarker and molecular testing (PDL-1 status, EGFR, ALK, ROS1, BRAF, NTRK, MET, HER2, KRAS, STK11, KEAP1). Descriptive statistics will be used to summarize the epidemiological characteristics.

Describe first-line NSCLC treatment patterns in Brazil real-world.

时间窗: Through study completation, an average of 2 years

The therapeutic choice: platinum-based therapy, ICI in monotherapy or combined, targeted therapy regimen for patients with driver mutations, TKI inhibitors, bi-specifics, ALK inhibitors, etc, will be extracted from medical records. Descriptive statistics will be used to summarize the treatment patterns.

Evaluate the concordance between the therapeutic choices and the BSCO guidelines.

时间窗: Through study completation, an average of 2 years

The concordance of real-life scenarios with the therapeutic guidelines of the Brazilian Society of Clinical Oncology (BSCO) will be assessed using Cohen's kappa coefficient.

次要结局

  • Describe of the epidemiological characteristics and first-line therapeutic patterns according all locally approved treatment approaches in NSCLC patients.(Through study completation,an average of 2 years)
  • Evaluate the influence of the mutational profile and PD-L1 expression on the choice of treatment.(Through study completation, an average of 2 years)
  • Evaluate the influence of clinical characteristics and mutational profile on the choice of first line treatment on EGFR mutated non-small cell lung cancer patients.(Through study completation, an average of 2 years)
  • Evaluate differences between patterns of choice in first-line treatment between generalist medical oncologists through an online survey.(Through study completation, an average of 2 years)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (7)

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