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Recruiting NCT07388771

Prediction of Outcome to Neoadjuvant Therapy in Non-small Cell Lung Cancer(NSCLC)

Observational NSCLC Neoadjuvant Therapy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: NSCLC, Neoadjuvant Therapy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Study on Multimodal Data Prediction of Outcome to Neoadjuvant Therapy in NSCLC

Overview

This observational study aims to construct and validate the performance of a multimodal predictive model in forecasting the outcomes of neoadjuvant therapy in patients with NSCLC. The core research question is: Can a multi-model approach predict outcomes of neoadjuvant therapy for non-small cell lung cancer and provide clinical recommendations?

Primary outcome measures

  • pathologic response [Time frame: Perioperative]
Secondary outcome measures (1)
  • EFS [Time frame: One year after the treatment ended]

Eligibility criteria

Inclusion criteria

  • pathologically diagnosed non-small cell lung cancer
  • The treatment plan is:receiving neoadjuvant chemo-immunotherapy during the study period, followed by surgical resection

Exclusion criteria

  • recurrent or metastatic lung cancer;
  • patients with other primary tumors

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 2 centers
  • Tongji hospital — Wuhan
  • Sir Run Run Shaw Hospital — Hangzhou

Identifiers

NCT: NCT07388771 · TJ-IRB202512147

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗