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Imaging Multiparametric/Multimodality for Lungcancer

Imaging Multiparametric/Multimodality (Magnetic Resonance Imaging Combined With Positron Emission Tomography) for Lungcancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02977663
Acronym
IRMomics
Enrollment
200
Registered
2016-11-30
Start date
2017-08-28
Completion date
2023-08-31
Last updated
2021-01-08

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

Conditions

Lungcancer

Brief summary

1. To build an imaging biobank of 200 patients with lungcancer, including pathologic and molecular characteristics of the tumor (mutational status, circulating DeoxyriboNucleic Acid (DNA) from serum biobank…), staging of the cancer (according to the new 2016 Tumor Node Metastasis (TNM) status, the table that classify non-small cell lungcancer) and follow-up informations (Response to first-line treatment (Response Evaluation Criteria in Solid Tumors (RECIST)), disease-free survival, 1-3 years survival). 2. To propose a simple severity scoring system based on tumor features such as size, doubling time (if available), location, amount of enhancement and necrosis. Such approach has been proposed for glioma evaluation (Visually Accessible Rembrandt Images (VASARI)) but is not available for the lung. The objective is to do better than the Tumor Node Metastasis (TNM) staging. 3. To develop and evaluate an IntraVoxel Incoherent Motion (IVIM) protocol for lungcancer evaluation.

Interventions

OTHERMagnetic Resonance Imaging (MRI)

* Chest MRI during the MRI cerebral * 2 tubes of blood taken during the medical visit

Sponsors

General Electric
CollaboratorINDUSTRY
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Adults over 18 years * High suspicion of lungcancer confirmed * Tumor \> 2 cm * Incomplete cerebral staging or not yet realized in the initial consultation of screening

Exclusion criteria

* Lungcancer medical history * During Pregnancy * Contraindications to MRI * Patient not able to understand the information of the protocol, taking into account the state of the brain * Patient unable to keep lying in MRI the necessary time

Design outcomes

Primary

MeasureTime frame
Event-free survival of patients with lungcancer3 years

Secondary

MeasureTime frame
Number of patients by histologic subtypes3 months, 1 year, 2 years and 3 years
Number of patients by mutational profile3 months, 1 year, 2 years and 3 years
Number of patients with metastases3 months, 1 year, 2 years and 3 years
Overall survival3 months, 1 year, 2 years and 3 years
Number of metastases by patient3 months, 1 year, 2 years and 3 years
Therapeutic responses assessed by scanner/MRI and/or Positron Emission Tomography (PET) based on consensus criteria (RECIST 1.1 and PET Response Criteria in Solid Tumors (PERCIST))3 months, 1 year, 2 years and 3 years
Number of patients with brain metastases3 months, 1 year, 2 years and 3 years

Countries

France

Contacts

Primary ContactSabine Helfen
sabine.helfen@aphp.fr33148957732

Outcome results

None listed

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