Effectiveness and Safety of Tisagenlecleucel Therapy in Brazilian Patients With B-lymphocyte Malignancies

This will be a multicenter, national, non-interventional, prospective cohort study Eligible participants will be pediatric (<18 years) and adult patients (aged 18 years or
older) with B-cell malignancies who have received tisagenlecleucel through the commercial
setting or out-of-specification (OOS) use in Brazil. We will collect data prospectively
and complement missing information with retrospective data collection, when necessary. It
is anticipated that approximately 200 patients will be enrolled in the cohort over 5
years divided among the study indications.

Since this is a non-interventional study, no administration of study drug or application
of questionnaires will be mandated by this protocol. The study will consist of a
"Pre-infusion" and a "Post infusion follow-up period" for up to 15 years post
tisagenlecleucel infusion. All patients will be followed until death or last scheduled
visit, whichever comes first.

For the study, "pre-infusion" and "follow-up post infusion" phases are defined as:

- "Pre-infusion" will consist of the patient's information from the time of diagnosis
untiljust prior to infusion with tisagenlecleucel.

- "Follow-up Post infusion" information will comprise any information from the
infusionof tisagenlecleucel onwards.