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RecruitingNCT06771960Updated Feb 21, 2025

Association Between RVT and Prognosis After Neoadjuvant Targeted Therapy in EGFR NSCLC

An observational study in Lung Cancer (NSCLC), sponsored by Guangdong Provincial People's Hospital. Recruiting at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-02-21.

Sponsored by Guangdong Provincial People's Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Feb 2025; still recruiting 1 year 8 months later.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
120
Ages
18 Years to 80 Years
Sex
All
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Study summary

EGFR-mutated NSCLC is a distinct subtype that responds well to targeted therapies. Neoadjuvant targeted therapy aims to downstage tumors and improve surgical outcomes, but the prognostic role of residual viable tumor (RVT) remains unclear. This retrospective study examines the association between RVT and survival outcomes. The findings will further validate the importance of RVT as a surrogate.

Read the detailed description

Non-small cell lung cancer (NSCLC) with EGFR mutations represents a molecularly distinct subset of lung cancer that benefits from targeted therapies. Neoadjuvant targeted therapy has emerged as a promising approach for locally advanced NSCLC, aiming to achieve tumor downstaging and improve surgical outcomes. However, the prognostic significance of residual viable tumor (RVT) after neoadjuvant targeted therapy remains poorly understood. This retrospective study investigates the association between the percentage of RVT and survival outcomes in EGFR-mutated NSCLC patients following neoadjuvant targeted therapy. Specific survival outcomes were disease-free survival (DFS) and event-free survival (EFS). By highlighting RVT as a critical prognostic biomarker, the findings provide actionable insights for optimizing postoperative management and stratifying high-risk patients. This work underscores the need for pathological evaluation of RVT to refine prognosis and treatment strategies.

02

Conditions studied

  • Lung Cancer (NSCLC)

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Keywords

  • lung cancer
  • Neoadjuvant targeted therapy
  • residual viable tumor
  • prognosis
  • EGFR-Mutated
03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's planned enrollment of 120 is below the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Guangdong Provincial People's Hospital is the lead sponsor of 231 studies on the registry; 101 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with EGFR-mutant NSCLC who received neoadjuvant targeted therapy followed by definitive surgery.

Inclusion criteria

  • Age 18-80 years old;
  • Pathologically diagnosed EGFR-mutated non-small cell lung cancer (NSCLC);
  • Treated with neoadjuvant targeted therapy;
  • Undergoing definitive surgery.

Exclusion criteria

Exclusion Criteria:

  • A history of prior chemotherapy, immunotherapy, or radiotherapy.
  • A history of malignancy or lung surgery;
  • Missing key data.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
120 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Disease-free survival (DFS)

    Disease-free survival (DFS) was defined as the time from the date of surgery to the date of recurrence or last follow-up.

    Time frame: Disease-free survival (DFS) was defined as the time from the date of surgery to the date of recurrence or last follow-up. Estimated final follow-up is 3 years postoperatively.

  2. Event-free survival (EFS)

    Event-free survival (EFS) was defined as the time from the date of diagnosis to the date of first event (relapse or death) or last follow-up.

    Time frame: Event-free survival (EFS) was defined as the time from the date of diagnosis to the date of first event (relapse or death) or last follow-up. Estimated final follow-up is 3 years postoperatively.

07

Study locations

1 of 1 sites recruiting
  • Guangdong Provincial People's Hospital
    Guangzhou, Guangdong 510080, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06771960
Lead sponsor
Guangdong Provincial People's Hospital
Responsible party
GuiBin Qiao (Prof., Guangdong Provincial People's Hospital) — Principal investigator
First posted
Jan 13, 2025
Start date
Feb 1, 2025
Primary completion
Dec 1, 2025 (estimated)
Completion
Dec 30, 2025 (estimated)
Last update
Feb 21, 2025

Study contacts

Guibin Qiao
Contact
guibinqiao@126.com
+86-13602749153
Guibin Qiao
principal investigator · Guangdong Provincial People's Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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