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Prognostic Role of Primary Non Small Cell Lung Carcinoma Standardized F18-FDG Uptake Values (SUV and TLG) Measured With F18-fluorodeoxyglucose Positron Emission Tomography (F18-FDG-PET): a Non Interventional Study.

Prognostic Role of Primary Non Small Cell Lung Carcinoma Standardized F18-FDG Uptake Values (SUV and TLG) Measured With F18-fluorodeoxyglucose Positron Emission Tomography (F18-FDG-PET): a Non Interventional Study.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00759382
Enrollment
340
Registered
2008-09-25
Start date
2008-07-31
Completion date
2022-01-31
Last updated
2021-08-23

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

Conditions

Non Small Cell Lung Carcinoma

Keywords

Non small cell lung carcinoma, PET scan, Observational study, Non metastatic, treated, curative intent

Brief summary

The primary aim of this non interventional study is to assess the independent prognostic role on overall survival of primary tumour 18F-FDG uptake value (SUVmax) measured on 18fluorodeoxyglucose positron emission tomography (18F-FDG-PET) in patients with non-metastatic non-small cell lung cancers treated with curative intent, taking into account the other conventional prognostic factors (performance status, age, sex, disease stage).

Interventions

None listed

Sponsors

European Lung Cancer Working Party
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Pathologically demonstrated NSCLC * Stage I-III treated by curative treatment by surgery with or without chemotherapy (induction or adjuvant) or by chemoradiotherapy * Inoperable patients treated by exclusive radiotherapy * A whole-body (skull base to mid thighs) FDG-PET or a combined FDG-PET/CT on a dedicated machine, performed before any anticancer treatment * FDG-PET or combined FDG-PET/CT has to be previously standardised according to the procedure described in appendix IV * Written informed consent * Accessibility to follow-up * Age \> 18 years

Exclusion criteria

* Prior anticancer treatment (surgery, radiotherapy or chemotherapy) * Stage IV NSCLC * A history of prior malignant tumour, except non-melanoma skin cancer or in situ carcinoma of the cervix and cured malignant tumour (more than 5-year disease free interval) * Uncontrolled diabetes mellitus (fast glycaemia above 130 mg/dl) * Pregnancy and lactating woman * Unavailability to send a copy of the PET or PET-CT (DICOM format) to the data centre

Design outcomes

Primary

MeasureTime frame
SurvivalSurvival will be dated from the date of PET scan

Secondary

MeasureTime frame
Progression-free survivalPeriod between the date of PET scan and the date of first progression or death

Other

MeasureTime frame
discriminant value of 18F-FDG uptake for survival and for PFSdated from PET examination

Countries

Belgium

Outcome results

None listed

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