Trials / Completed
CompletedNCT01248000
The Use of FDG-PET in Patient With Hodgkin Lymphoma: a Population Based Study From Northern Italy
The Use of FDG Positron Emission Tomography (PET)in Patient With Hodgkin Lymphoma (HL) in the "Real World": a Population Based Study From Northern Italy
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 136 (actual)
- Sponsor
- Gruppo Italiano Studio Linfomi · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Positron Emission Tomography (PET) represents a step forward in the definition of response to therapy in patients with Hodgkin Lymphoma (HL). In particular the use of PET for the early assessment of response has been described as the most important tool for predicting the risk of disease progression. As no data are available to support the use of early assessment of response for adapting and modifying subsequent treatment, the use of PET should be limited only to patients enrolled in clinical trials. Irrespective of recommendations PET scanning is included in the current management of patients with HL at baseline, mid treatment, end of treatment, and follow-up. So far no study has been performed to verify how PET is currently used in the clinical setting and to assess if and how results of PET scanning are used for supporting treatment and clinical decisions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | FDG-PET | PET interpretation is based on a site-to-site comparison of FDG uptake both before and after chemotherapy (qualitative approach), according to the criteria defined by Cheson (2008) |
Timeline
- Start date
- 2009-05-01
- Completion
- 2010-05-01
- First posted
- 2010-11-25
- Last updated
- 2010-11-25
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT01248000. Inclusion in this directory is not an endorsement.