Study of Low Dose CT in Sarcoma Patients

University Health Network, Toronto

Status and phase

Completed

Phase 1

Conditions

Soft Tissue Sarcoma

Treatments

Procedure: low dose CT

Study type

Interventional

Funder types

Other

Identifiers

NCT00188422

03-0468-CE

Details and patient eligibility

About

The primary outcome of this study is the detection of lung metastases comparing Low dose CT (LDCT) and Minimum dose CT (MnDCT) with CXR.

Hypothesis

LDCT and MnDCT have similar sensitivity for the detection of lung nodules (metastases).
MnDCT of the thorax detects a larger number of nodules (metastases) than CXR.

Full description

A 3-year prospective phase II non-randomized study commenced May 2003 enrolling 60 high-risk patients with Intermediate and High Grade STS. Each patient is kept under radiological surveillance for 3 years unless lung metastases are detected. Conventional thoracic imaging for staging and surveillance of STS patients is shown in Figure 1. In the trial, LDCT and MnDCT are added to each imaging visit (Figure 1). A 2-view CXR (CR) is performed (Direct View, Kodak, Rochester) followed by thoracic CT scans performed on a Siemens 16 row MDCT (Sensation 16, Siemens, Erlangen), CT acquisition; 120kVp, 5/2.5/2.5mm. Images are reconstructed with high and low spatial frequency filters and soft copy viewing is performed on a standalone PACS workstation using standard mediastinal (w 350, l 40) and lung (w 1500, l -600) settings. Examinations are performed with varying mAs; SDCT 120 mAs, LDCT 40 mAs and MnDCT 20 mAs. The examinations are evaluated, blinded to the results of the alternative and previous studies, for the presence of nodules (defined as a non-calcified focal opacity ≥3 mm < 3 cm). Surveillance imaging is commenced 3 months post surgery.

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria