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Real World Study on Erlotinib/Gefitinib Combined With Bevacizumab in Advanced Non-aquamous Non-small Cell Lung Cancer

Real World Study to Evaluate the Efficacy and Resistant Mechanism of Erlotinib/Gefitinib Combined With Bevacizumab in First Line EGFR Mutation Positive Advanced Non-aquamous Non-small Cell Lung Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03647592
Enrollment
30
Registered
2018-08-27
Start date
2018-06-01
Completion date
2025-12-01
Last updated
2023-12-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Small Cell Lung Cancer

Keywords

Non-small Cell Lung Cancer, Bevacizumab, Erlotinib/Gefitinib, EGFR mutation positive

Brief summary

This study aims to explore the efficacy and safety of Erlotinib/Gefitinib combined with bevacizumab in the real world for advanced non-squamous cell lung cancer with EGFR mutation, explore new drug resistance mechanisms under the A+T regimen and consistency between plasma and tissue detection driving genes, and finally assess the predictive value of plasma dynamic detection driving gene mutation profiles in predicting disease. The role of disease progression risk.

Detailed description

A retrospective study of 30 cases of advanced non-squamous non-small cell lung cancer (NSCLC) with EGFR mutation positive treated with A+T was conducted to observe the efficacy and safety of A+T regimen in the real world. Exploratory research contents are as follows: 1. Consistency between tissue gene test (NGS) and plasma gene test (NGS) at the initial diagnosis; 2. Consistency between tissue gene test (NGS) and plasma gene test (NGS) at the progression of A + T treatment; 3. New drug resistance mechanism of A + T treatment; 4. Plasma dynamics during A + T treatment. Detection (the first efficacy evaluation and a blood sampling before imaging PD) exploration and imaging progress sequence; 5. Plasma large panel dynamic drive gene mutation spectrum analysis to build disease progression risk model.

Interventions

DRUGErlotinib/Gefitinib combined with Bevacizumab

Erlotlnib,150mg po qd/gefitinib 250mg po qd +Bevacizumab(15mg/kg),lvgtt,every 21 day ,evaluate every 2 months

Sponsors

Hunan Province Tumor Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* EGFR mutation(19del/L858R) * advanced non-saquamous non-small cell lung cancer * primary treatment of first diagnosis * performance status(0-1)

Exclusion criteria

* other genes mutation * saquamous

Design outcomes

Primary

MeasureTime frameDescription
PFSApproximately 1 yearsProgression free survival

Secondary

MeasureTime frameDescription
OSApproximately 1 yearsOverall survival
DCRApproximately 1 yearsDisease control rate

Countries

China

Contacts

Primary ContactYongchang Z MD, MD
zhangyongchang@csu.edu.cn+8613873123436
Backup ContactYongchang Z MD, PhD
zhangyongchang@csu.edu.cn+8613873123436

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026