Actively Recruiting

Age: 18Years +
All Genders
ID07519356

A Comprehensive Register Of Lymphoproliferative Disorders (ReLy)

Led by Fondazione IRCCS Policlinico San Matteo di Pavia · Updated on 2026-04-09

9000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational study focuses on patients aged 18 and older who have lymphoproliferative disorders, a group of blood cancers affecting the lymphatic system. Researchers aim to understand the overall survival over 10 years for different types of these disorders. The study also examines factors like patient fitness, comorbid conditions, and how these influence treatment choices and outcomes. New therapies including chemo-free protocols, targeted drugs, and cell therapies are being evaluated to determine the best treatment sequences for cases that are refractory or relapsed. Participants will be observed through various phases of their disease, including diagnosis and treatment stages. The study investigates the impact of clinical and biological factors on disease progression or relapse, as well as potential links between genetic profiles and clinical outcomes. It also monitors adverse events like tumor lysis syndrome and their effects on treatment adjustments. Additionally, the study looks at patients managed with a watch-and-wait approach, long-term toxicities, secondary cancers, and healthcare resource use. Throughout the study, participants' health and treatment outcomes will be regularly assessed using clinical data collected from diagnosis through follow-up. Researchers will analyze survival rates, treatment effectiveness, and side effects over a long period from 2002 to 2030. This comprehensive data collection aims to improve understanding of lymphoproliferative disorders and optimize patient management strategies over time.

CONDITIONS

Brief Title

A Comprehensive Register Of Lymphoproliferative Disorders (ReLy)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years or older diagnosed with or treated for lymphoproliferative disorders.
  • Prospective patients or their legal guardians able to understand and willing to sign a written informed consent document.
  • Retrospective patients who have signed the institutional document allowing use of their data for research.
Not Eligible

You will not qualify if you...

  • Patients unable to understand the informed consent document.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 28 years

Participants are observed over time to evaluate overall survival and disease progression of lymphoproliferative disorders.

Periodic visits based on clinical follow-up and data collection schedules

Trial Site Locations

Total: 1 location

1

Fondazione IRCCS Policlinico San Matteo

Pavia, Lombardy, Italy, 27100

Actively Recruiting

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Research Team

L

Luca Arcaini

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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