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Recruiting NCT06742021

Application of DCE-MRI Based on 4D FreeBreathing in Predicting the Efficacy of Immune and Targeted Therapy in Lung Cancer

No phase Interventional Lung Cancer

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
The protocol lists: Application Value of MRI Imaging in Treatment Decision-Making for Lung Cancer.
Who it may be relevant to
Registry conditions: Lung Cancer. Basic parameters: 18 years — 75 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 →

Overview

This study aims to address the challenge of predicting the efficacy of targeted and immunotherapy in lung cancer patients. By utilizing two DCE-MRI images-one before treatment and one after one treatment cycle-along with the patients' clinical and pathological information, we aim to achieve accurate prediction of the therapeutic efficacy of targeted and immunotherapy in lung cancer patients.

Interventions

  • Diagnostic test Application Value of MRI Imaging in Treatment Decision-Making for Lung Cancer
    Chest MRI scans outside of the standard treatment protocol

Primary outcome measures

  • Tumor treatment response evaluation [Time frame: within one week before treatment and two weeks after treatment completion]

Eligibility criteria

Inclusion criteria

  • Tumor size greater than 2 cm
  • Age between 18 and 75 years

Exclusion criteria

  • Presence of MRI contraindications (e.g., metal implants, pacemaker implantation, etc.)
  • Allergy to gadolinium contrast agents
  • Lesions difficult to delineate on images due to conditions such as atelectasis or diffuse lesions

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

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • Yunnan Cancer Hospital — Kunming

Identifiers

NCT: NCT06742021 · KYLX2024-272

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗