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18FDG-PET in Patients With Melanoma or NSCLC Treated With Immunotherapy

18FluoroDeoxyGlucose-Positron Emission Tomography (PET) in Patients With Melanoma or Non Small Cell Lung Cancer Treated With Immunotherapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03741231
Acronym
IMMUNOPET
Enrollment
70
Registered
2018-11-14
Start date
2018-03-01
Completion date
2018-06-30
Last updated
2019-05-06

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

Conditions

18F-FDG, Immunotherapy, Melanoma, NSCLC, Positron-Emission Tomography

Keywords

melanoma, NSCLC, FDG, PET, immunotherapy

Brief summary

Study the EFS and OS according to 18FDG PET in patients with melanoma or non small cell lung cancer treated by immunotherapy.

Detailed description

Study EFS in patients with melanoma or NSCLC treated by immunotherapy (anti CTLA4 or anti PDL1) and performed18FDG PET Multicentric retrospective study

Interventions

None listed

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* patients treated for melanoma or NSCLC with immunotherapy (anti CTLA4 or antiPDL1) * patients treated in Brest, Morlaix, Landerneau hospital * patients performed FDG PET * no opposition to study

Exclusion criteria

* age under 18 years old * refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
measure of progression free survival (obtained by the delay between the date of initiation of immunotherapy until the date of first documented progression disease in patients with melanoma or NSCLC treated by immunotherapyup to 50 monthsFrom date of initiation of treatment until the date of first documented progression disease according to different criteria in interim PET/CT 1. 18F-FDG PET/CT imaging was performed prior to (18F-FDG PET/CT 0) and 14 weeks after ICI onset (18F-FDG PET/CT 1). Assessment of patient response to treatment was done according to RECIST1.1, iRECIST, PERCIST and PECRIT criteria.

Secondary

MeasureTime frameDescription
measure of overall survival (obtained by the delay between the date of initiation of immunotherapy until the date of death related to disease in patients with melanoma or NSCLC treated by immunotherapyup to 50 monthsFrom date of initiation of treatment until the date of death related to disease according to different criteria in interim PET/CT 1. 18F-FDG PET/CT imaging was performed prior to (18F-FDG PET/CT 0) and 14 weeks after ICI onset (18F-FDG PET/CT 1). Assessment of patient response to treatment was done according to RECIST1.1, iRECIST, PERCIST and PECRIT criteria.
Study different criteria (RECIST, iRECIST, PERCIST and PECRIT) to predict PFS or OSup to 50 monthsInterpretation according to 4 criteria to predict response to immunotherapy
study the potential correlation between PET data and clinicobiological dataup to 50 monthscorrelation between adverse events (AE) due to immunotherapy described on PET data and AE detected on clinicobiological data

Countries

France

Outcome results

None listed

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