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Study identifier: NCT06822855 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Changing Paragidms In The Prognostic Assessment Of Hodgkin Lymphoma

Condition: Classical Hodgkin Lymphoma · Classical Hodgkin Lymphoma Recurrent · Classical Hodgkin Lymphoma Refractory  ·  Sponsor: Azienda USL Reggio Emilia - IRCCS

PhaseN/A
Planned participants755
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Classical Hodgkin's Lymphoma (cHL) is a rare but highly treatable malignancy of the immune system, primarily affecting young adults. Despite significant therapeutic advancements, frontline treatment failure occurs in up to 30% of cases, with relapse or refractory disease affecting over 50% of these patients. The main therapeutic challenge in cHL remains achieving an optimal balance between disease control and reducing long-term adverse effects. Current prognostic tools only partially capture patient heterogeneity, and cHL continues to evolve spatially and temporally throughout the course of the disease. Personalized treatment strategies require novel integrated tools that better monitor tumor complexity and anticipate disease progression. Fluorodeoxyglucose positron emission tomography (FDG-PET) has improved risk stratification in cHL, as metabolic response during or after chemotherapy strongly correlates with disease progression and survival. However, FDG-PET has limitations, including the absence of standardized criteria and the necessity to initiate treatment before response assessment. To overcome these limitations, molecular profiling and radiomic analysis of baseline FDG-PET data may provide deeper insights into tumor biology, improving prognostic accuracy. This observational study aims to dissect the genetic and phenotypic heterogeneity of cHL at diagnosis and during disease evolution, with the goal of identifying novel prognostic biomarkers. These findings could lea…

This description comes directly from the study's public registry record.

Talk to the study team

Attilio Gennaro, Clinical Research Coordinator  ·  +39 0522 295175  ·  attilio.gennaro@ausl.re.it

Always discuss trial participation with your own doctor first.

Locations (12)

ASST Grande Ospedale Metropolitano NiguardaMilan, MI, ItalyRecruiting
Azienda USL IRCCS di Reggio EmiliaReggio Emilia, RE, ItalyRecruiting
A.O.S.G. MoscatiAvellino, ItalyRecruiting
Spedali Civili BresciaBrescia, ItalyRecruiting
Istituto Oncologico VenetoPadova, ItalyRecruiting
Azienda Ospedaliera "Ospedali Riuniti Villa Sofia-Cervello"Palermo, ItalyRecruiting
Azienda Ospedaliera di PerugiaPerugia, ItalyRecruiting
Ospedale S. Maria della Misericordia, Azienda Ospedaliera di PerugiaPerugia, ItalyRecruiting
AUSL PiacenzaPiacenza, ItalyRecruiting
Azienda Ospedaliera Santa Maria - TerniTerni, ItalyRecruiting
AOU Città della salute e della Scienza, "Le Molinette"Torino, ItalyRecruiting
AOU Città della Salute e della ScienzaTorino, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06822855