FDG PET Evaluation for Marginal Zone Lymphoma and Its Prognostic Role
Launched by INTERNATIONAL EXTRANODAL LYMPHOMA STUDY GROUP (IELSG) · Apr 2, 2020
Trial Information
Current as of July 16, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the use of PET scans in patients with Marginal Zone Lymphoma (MZL). The goal is to see how well PET scans help in staging the disease, assessing how well treatment is working, and predicting patient outcomes. The study will look back at patients who have already had PET scans as part of their diagnosis or treatment, and it will analyze these scans alongside other tests like CT scans and lab results to understand their effectiveness.
To participate in this trial, you need to be an adult over 18 years old and have a confirmed diagnosis of one of the specific types of MZL. Additionally, your medical records should include details about your treatment and follow-up, and you must have had the required imaging tests. Importantly, this study does not require any new scans or procedures; it will only use information and scans that have already been done. If you join the trial, you will help researchers learn more about how PET scans can improve the care and treatment of MZL patients in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- 1. One of the following subtypes of Histology confirmed Indolent non-follicular B-cell lymphoma:
- • Splenic MZL (bone marrow histology and/or splenic tissue);
- • Extranodal MZL or MALT (tissue biopsy);
- • Nodal MZL (lymph node biopsy).
- • 2. Age over 18.
- • 3. Availability of details on clinical presentation, treatment details and results, and on follow-up.
- • 4. Execution of PET at diagnosis or/and at end of treatment or/and at relapse.
- • 5. Execution of CT scan with iodine contrast medium at diagnosis and at assessment of response.
- • 6. Patients with histologically confirmed marginal zone lymphomas according to the current WHO classification are registered in the study. Diagnosis based on tru-cut core-needle biopsies are permitted in the study.
- • 7. Written informed consent.
- Exclusion Criteria:
- • 1. Patients with a diagnosis of Non Hodgkin Lymphoma other than MZL.
- • 2. Scans images not available for whatever reason.
- • 3. Cases diagnosed on fine needle aspiration cytology only.
About International Extranodal Lymphoma Study Group (Ielsg)
The International Extranodal Lymphoma Study Group (IELSG) is a collaborative network dedicated to advancing the understanding and treatment of extranodal lymphomas through rigorous clinical research. Comprising a diverse group of international experts, the IELSG focuses on designing and conducting multicenter clinical trials aimed at improving patient outcomes and establishing evidence-based treatment protocols. By fostering collaboration among leading oncologists, researchers, and institutions, the IELSG strives to enhance the knowledge of extranodal lymphomas, promote innovative therapeutic strategies, and ultimately improve the quality of care for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Dijon, , France
Dijon, , France
Paris, , France
Napoli, , Italy
Milan, Mi, Italy
Milan, Mi, Italy
Toulouse, , France
Ponderano, Bi, Italy
Bari, , Italy
Alessandria, Al, Italy
Cagliari, Ca, Italy
Catania, Ct, Italy
Milan, Mi, Italy
Palermo, Pa, Italy
Padova, Pd, Italy
Pescara, Pe, Italy
Aviano, Pn, Italy
Pavia, Pv, Italy
Torino, To, Italy
Terni, Tr, Italy
Varese, Va, Italy
Verona, Vr, Italy
Reggio Emilia, , Italy
Geneva, Ge, Switzerland
Bellinzona, Ti, Switzerland
Candiolo, To, Italy
Patients applied
Trial Officials
Stefano Luminari, MD
Study Chair
AUSL IRCCS - Reggio Emilia (Italy)
Catherine Thieblemont, MD
Study Chair
Saint-Louis Hospital, Paris, France
Emanuele Zucca, MD
Study Chair
Oncology Institute of Southern Switzerland
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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