About this trial

This phase II trial studies how well inotuzumab ozogamicin works in treating younger patients with B-lymphoblastic lymphoma or CD22 positive B acute lymphoblastic leukemia that has come back (relapsed) or does not respond to treatment (refractory). Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a toxic agent called ozogamicin. Inotuzumab attaches to CD22 positive cancer cells in a targeted way and delivers ozogamicin to kill them.

Eligibility criteria

Qualifiers

Patients must be >= 1 year and < 22 years of age at the time of enrollment

Patients must have B-ALL, or previously diagnosed B lymphoblastic lymphoma (B-LL), with >= 5% (M2 or M3) bone marrow blasts with or without extramedullary disease

NOTE: Relapsed patients previously diagnosed with B-lymphoblastic lymphoma (B-LL) are eligible if they have an M2 or M3 marrow at the time of enrollment on this study

Patients with ALL or B-LL who have M2 morphology must have local confirmatory testing showing >= 5% blasts by flow cytometry, fluorescence in situ hybridization (FISH) testing or other molecular method

Disqualifiers

Cytotoxic chemotherapy or other anti-cancer agents known to be myelosuppressive. For agents not listed, the duration of this interval must be discussed with the study chair and the study-assigned Research Coordinator prior to enrollment.

A waiting period prior to enrollment is not required for patients receiving standard cytotoxic maintenance chemotherapy (i.e., corticosteroid, vincristine, 6MP, and/or methotrexate).

A waiting period is not required for patients receiving a single dose of intrathecal methotrexate, hydrocortisone, and/or cytarabine within 7 days prior to enrollment

>= 14 days must have elapsed after the completion of other cytotoxic therapy, with the exception of hydroxyurea, for patients not receiving standard maintenance therapy. For patients who previously received calaspargase pegol, >= 21 days must have elapsed after the last dose. Additionally, patients must have fully recovered from all acute toxic effects of prior therapy.

Trial design

Treatments tested in this trial

  • Asparaginase Erwinia chrysanthemi
  • Biospecimen Collection
  • Bone Marrow Aspiration and Biopsy
  • Calaspargase Pegol
  • Cyclophosphamide
  • Cytarabine
  • Diagnostic Imaging Testing
  • Inotuzumab Ozogamicin
  • Leucovorin Calcium
  • Lumbar Puncture
  • Methotrexate
  • Pegaspargase
  • Vincristine

Treatment groups

80 Participants
are divided into 2 treatment groups

Locations

157
Puerto Rico
HIMA San Pablo Oncologic Hospital00726, Caguas Puerto Rico
United States
Alabama
Children's Hospital of Alabama35233, Birmingham United States
Alaska
Providence Alaska Medical Center99508, Anchorage United States
Arizona
Banner Children's at Desert85202, Mesa United States

Sponsors and collaborators

Children's Oncology Group

Lead sponsor

National Cancer Institute (NCI)

Collaborator