Adult Acute Lymphoblastic Leukemia Treated With Pediatric Regimen in Brazil

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16-50
SponsorInstituto do Cancer do Estado de São Paulo

About this trial

In this project, the investigators intend to start a prospective registry for patients with newly diagnosed Philadelphia-negative ALL from 16 years old and above in participating centers, provided that all patients will be treated with the same regimen (a pediatric regimen BFM-based incorporating peg-asparaginase). All diagnostic/follow-up (after induction and consolidation blocks) samples will be centrally biobanked at Instituto do Cancer do Estado de Sao Paulo. The main goal of this study is to examine whether the implementation of a pediatric protocol under a prospective registry can increase event-free survival (EFS) and overall survival (OS) of newly diagnosed patients in the participating centers.

Eligibility criteria

Qualifiers

None

Disqualifiers

Burkitt leukemia

Prior myeloproliferative disease

Philadelphia chromosome positivity through whichever methodology (RT-PCR, FISH, or conventional karyotype)

ECOG>2 (appendix 3)

Trial design

Treatments tested in this trial

  • Prednisone
  • Vincristin
  • Daunorubicin
  • Peg-asparaginase
  • Intrathecal Suspension
  • Cyclophosphamide
  • Cytarabine
  • Mercaptopurine
  • Methotrexate
  • Doxorubicin

Treatment groups

180 Participants
are divided into 1 treatment group

Sponsors and collaborators