NCT07519356

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
9,000

participants targeted

Target at P75+ for all trials

Timeline
53mo left

Started Jun 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress49%
Jun 2022Dec 2030

Study Start

First participant enrolled

June 9, 2022

Completed
3.8 years until next milestone

First Submitted

Initial submission to the registry

April 2, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 9, 2026

Completed
4.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2030

Last Updated

April 9, 2026

Status Verified

April 1, 2026

Enrollment Period

8.6 years

First QC Date

April 2, 2026

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Lymphoproliferative Disorders

Condition Hierarchy (Ancestors)

Lymphatic DiseasesHemic and Lymphatic DiseasesImmunoproliferative DisordersImmune System Diseases

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

Locations