A Comprehensive Register Of Lymphoproliferative Disorders (ReLy)
1 other identifier
observational
9,000
1 country
1
Brief Summary
The primary objective of this study is to assess the 10-year overall survival (OS) of patients with different lymphoproliferative disorders. Secondary objectives include evaluating the comorbidities and fitness of patients and their impact on treatment choices and outcomes. Additionally, the study will examine the effectiveness of various therapeutic regimens, with a particular focus on new treatments, such as chemo-free protocols, targeted drugs, and cell therapies, in order to determine the best treatment sequence for refractory and relapsed cases. The research will also investigate how clinical and biological factors influence disease progression or relapse. Another aim is to explore potential correlations between genotype, clinical phenotype, and outcomes, both at diagnosis and during various disease stages. The study will also assess the incidence of tumor lysis syndrome and other adverse events during treatment, considering how these factors might affect treatment discontinuations or dose reductions. Another objective is to evaluate the outcomes of patients who are managed with a "watch and wait" approach. Long-term toxicities and the occurrence of secondary malignancies will also be studied, alongside the analysis of healthcare costs and the resources used in patient management.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2022
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 9, 2022
CompletedFirst Submitted
Initial submission to the registry
April 2, 2026
CompletedFirst Posted
Study publicly available on registry
April 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 30, 2030
April 9, 2026
April 1, 2026
8.6 years
April 2, 2026
April 2, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
To evaluate 10 year overall survival (OS) of each lymphoproliferative disorder.
from 2002 to 2030
Study Arms (5)
LNH B
malignant tumor of the lymphatic system originating from the uncontrolled proliferation of B lymphocytes,
LNH T/NK
A heterogeneous and rare group of blood cancers (hematological malignancies) that originate from the malignant transformation of mature T lymphocytes or natural killer (NK) cells.
Hodgkin
It is a tumor of the lymphatic system, characterized by the presence of Reed-Sternberg cells, which usually originates in the lymph nodes.
Immunodeficiency-associated
conditions characterized by abnormal lymphoid tissue growth, ranging from benign to malignant lymphomas, resulting from immune dysregulation
Hystiocitic and dendritic cell neoplasms
a rare, heterogeneous group of hematologic malignancies originating from the mononuclear phagocyte system (monocytes, macrophages, and dendritic cells)
Eligibility Criteria
Patients ≥ 18 years diagnosed with and/or treated for lymphoproliferative disorders.
You may qualify if:
- Patients ≥ 18 years diagnosed with and/or treated for lymphoproliferative disorders.
- Prospective patients (or their or legal guardians) who have the ability to understand and be willing to sign a written informed consent document
- Retrospective patients who have signed the institutional document allowing the use of their data for research on their disease
You may not qualify if:
- Patients who are unable to understand informed consent document
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fondazione IRCCS Policlinico San Matteo
Pavia, Lombardy, 27100, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Target Duration
- 10 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
April 2, 2026
First Posted
April 9, 2026
Study Start
June 9, 2022
Primary Completion (Estimated)
December 30, 2030
Study Completion (Estimated)
December 30, 2030
Last Updated
April 9, 2026
Record last verified: 2026-04