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NCT04206787Completed

The Study Observes Afatinib as First-line Treatment in Patients With Epidermal Growth Factor Receptor (EGFR) Mutation-positive Advanced Non-small Cell Lung Cancer

Real-world Study on Afatinib as First-line Treatment in Patients With Epidermal Growth Factor Receptor (EGFR) Mutation-positive Advanced Non-small Cell Lung Cancer (NSCLC)

Source: ClinicalTrials.gov · Last updated 28 Feb 2025

Brief summary (registry, in English)

This study aims to observe the sequential strategy with afatinib as first-line treatment and to find the optimal treatment strategy for long-term chemotherapy-free regimens in Chinese patients with EGFR-mutated advanced NSCLC. Furthermore, this study can also assess the effectiveness and safety of afatinib as first-line treatment.

Status (registry)
Completed
Study type
Observational
Enrollment
72 (actual)
First submitted
11 Dec 2019
Start date
20 May 2020
Primary completion date
18 Dec 2023
Lead sponsor
Boehringer Ingelheim
Diseases
Lung cancer
NCT number
NCT04206787

What you commit to

  • Study type: Observational
  • Participants enrolled: 72
  • From 20 May 2020 to the primary completion date, 18 Dec 2023
  • 10 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have received previous systemic therapy (previous adjuvant or neoadjuvant therapies are permitted)
  • Patients with symptomatic brain metastases (patients with brain metastases, who were previously treated, are eligible provided they have asymptomatic brain metastasis for at least 4 weeks on stable doses of medication) at the start of afatinib treatment
  • Patients with concurrent participation in an interventional oncology clinical trial during the first-line treatment phase or within the last 30 days prior to the first-line treatment phase. If patients join another interventional study during the period of second-line treatment or later-line treatment, this patient should not be excluded from this study

Who the study is looking for

  • Patients who are diagnosed with locally advanced or metastatic NSCLC with EGFR sensitive mutation positive
  • Patients who will initiate afatinib as first-line treatment for EGFR mutation-positive NSCLC
  • Male and female patients with age ≥18 years
  • Written informed consent per local regulatory requirement

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking Union Medical College Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
West China Hospital
Coordinator of this site? Confirm its status
ChengduChinaUnknown status
First Affiliated Hospital of Guangzhou Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status
The First Afiliated Hospital, Sun Yet-sen University
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status
Hainan Cancer Hospital
Coordinator of this site? Confirm its status
HaikouChinaUnknown status
The First Affiliated Hospital, Zhejiang University
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status
China Shenyang Chest Hospital
Coordinator of this site? Confirm its status
ShenyangChinaUnknown status
Shenzhen People's Hospital
Coordinator of this site? Confirm its status
ShenzhenChinaUnknown status
The First Affiliated Hospital of Zhengzhou Unviersity
Coordinator of this site? Confirm its status
ZhengzhouChinaUnknown status
Zhongshan People's Hospital
Coordinator of this site? Confirm its status
ZhongshanChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.