High Risk, Hodgkin Lymphoma, Relapse
Conditions
Brief summary
Cohort study enrolled high-risk Hodgkin Lymphoma patients in first relapse after induction therapy followed after remission either with a systemic imaging-based surveillance (Imaging cohort) or with standard clinical-based surveillance (standard cohort).
Interventions
DIAGNOSTIC_TESTStandard cohort: Clinical lab follow-up
DIAGNOSTIC_TESTImaging cohort: integrated imaging follow-up
Sponsors
Federico II University
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* High risk Hodgkin Lymphoma * achievement of complete response to first line therapy
Exclusion criteria
* comorbidities that could impair participation in follow-up procedures
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Event Free Survival (EFS) | Time period from the first relapse after induction therapy to the date of an event (refractoriness, relapse, or death) or the last follow-up visit after autologous stem cell transplantation (ASCT), up to 2 years | Events: * refractoriness * relapse * death |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| EFS for clinically silent relapses | Time period from the first relapse after induction therapy to the date of an event (refractoriness, relapse, or death) or the last follow-up visit after autologous stem cell transplantation (ASCT), up to 2 years | Events: * refractoriness * relapse * death |
| Response rate | After salvage therapy and autologous stem cell transplantation (ASCT), up to 2 years | Rate of response |
Outcome results
None listed