Bergamo Lymphoid Cancer Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorA.O. Ospedale Papa Giovanni XXIII

About this trial

This registry has been established to gain a better understanding of the clinical and biological characteristics and outcome of patients with lymphoid cancer

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female patients 18 years or older

Written informed consent

Confirmed diagnosis of Hodgkin disease, non-Hodgkin lymphomas or myeloma

Disqualifiers

None

Trial population

Patients eligible for this study are patients with a diagnosis of lymphoid cancer in charge of the Hematology and Bone Marrow Transplant Unit "Ospedale Papa Giovanni XIII" of Bergamo.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Patient registry

    Other intervention

    Clinical data, specific procedures and treatments will follow the Institutional standard operative procedures

Treatment groups

6,000 Participants
are divided into 3 treatment groups
Group A: Hodgkin lymphoma1 intervention
Group B: Non-Hodgkin lymphoma1 intervention
Group C: Myeloma1 intervention

Trial outcomes

Primary outcomes

1

Overall survival

Analyzed for all patients as time from diagnosis to death as a result of any cause, stratified according to intervention and baseline characteristics

Time frame
20 years

Secondary outcomes

1

Disease-free survival

Analyzed only for patients in complete response, as time from achievement of the complete response to relapse or death due to disease or acute toxicity of treatment, stratified according to intervention and baseline characteristics

Time frame
20 years
2

Progression-free survival

Analyzed for all patients, as time from diagnosis to progression of disease or death as a result of any cause, stratified according to intervention and baseline characteristics

Time frame
20 years
3

Biological correlative studies

Association between clinical and biologic characteristics

Time frame
20 years

Other outcomes

Sponsors and contacts

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