Clinical Trials Directory

Trials / Completed

CompletedNCT00351598

Lung Tumour Volume Database

Tumour Volume as an Independent Prognostic Factor in Patients With Non-Small Cell Lung Cancer - A Protocol for a Prospective Database.

Status
Completed
Phase
Study type
Observational
Enrollment
531 (actual)
Sponsor
Trans Tasman Radiation Oncology Group · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main aim is to determine, in patients with locoregional, non-small cell lung cancer (NSCLC) treated by definitive radiotherapy, the influence on survival of the volume of primary tumour, as measured from CT imaging, after adjusting for the effect of the current TNM staging system and other known prognostic factors (especially ECOG performance and weight loss).

Detailed description

Patients with locoregional non small cell lung cancer are registered on study after tumour volumes are outlined by a radiologist and prior to the commencement of any treatment. All patients must have recorded the volume of disease in the primary tumour (and of involved nodes \> 1 cm diameter) as measured from a CT scan performed according to a standard set of conditions. Following registration patients are treated with Definitive radiotherapy with or without chemotherapy. Follow-up will occur with the collection of a minimum amount of data every 12 months from the date of registration on study. Quality Assurance procedures will be implemented with each site that participates in the study.

Conditions

Interventions

TypeNameDescription
RADIATIONDefinitive Radiotherapy60Gy in 6 weeks, 50Gy in 4 weeks. Each individual fraction should not exceed 2.5Gy.

Timeline

Start date
1999-09-01
Primary completion
2009-02-01
Completion
2012-11-01
First posted
2006-07-13
Last updated
2014-08-04

Locations

15 sites across 3 countries: Australia, New Zealand, Singapore

Source: ClinicalTrials.gov record NCT00351598. Inclusion in this directory is not an endorsement.