About this trial
This is a purely retrospective and observational monocentric study
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Marginal zone lymphoma patients who were diagnosed and treated in our Hospital between December 2012 and December 2018.
Age ≥ 18 years at enrolment.
Written informed consent (if applicable)
Disqualifiers
none
Trial population
Marginal zone lymphoma patients who were diagnosed and treated in our Hospital between December 2012 and December 2018
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
clinical characteristics of Marginal zone lymphoma patients
to descrive clinical characteristics of Marginal zone lymphoma patients who were diagnosed and treated in our Hospital.
Secondary outcomes
effectiveness
It includes: 1. Description of treatment duration and causes of treatment discontinuation. 2. Description of adverse events / safety of the treatments 3. Assessment of patients' survival. 4. Description of the medical resource utilization, including number of emergency department visits, hospitalizations, use of hematopoietic growth factors and antibiotics, and blood product transfusions. 5. Patient clinical and biological characteristics and disease biological profile at baseline of Marginal zone lymphoma cases
safety
It includes: 1. Description of treatment duration and causes of treatment discontinuation. 2. Description of adverse events / safety of the treatments 3. Assessment of patients' survival. 4. Description of the medical resource utilization, including number of emergency department visits, hospitalizations, use of hematopoietic growth factors and antibiotics, and blood product transfusions. 5. Patient clinical and biological characteristics and disease biological profile at baseline of Marginal zone lymphoma cases
Sponsors and contacts
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