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Multiagent chemotherapy in relapsed acute lymphoblastic leukemia in children
J B Belasco1, N Luery, C Scher
1Division of Oncology, Children's Hospital of Philadelphia, Pennsylvania 19104.
Cancer
|December 15, 1990
Summary
This study treated children with relapsed acute lymphoblastic leukemia (ALL) using intensive chemotherapy. While many achieved remission, long-term event-free survival remained low, with less than 20% alive after five years.
Area of Science:
- Pediatric Oncology
- Hematology
- Cancer Chemotherapy
Background:
- Acute lymphoblastic leukemia (ALL) is a common childhood cancer.
- Relapse of ALL presents significant treatment challenges.
- Effective salvage therapies for pediatric ALL relapse are crucial.
Purpose of the Study:
- To evaluate the efficacy of an intensive induction, consolidation, and maintenance chemotherapy regimen for children with early first bone marrow relapse of ALL.
- To assess event-free survival (EFS) and overall survival rates in this patient cohort.
Main Methods:
- Twenty-seven evaluable children with early first bone marrow relapse of ALL received a 35-day induction regimen (daunomycin, vincristine, prednisone, teniposide, cytosine arabinoside, L-asparaginase) followed by maintenance therapy.
- Intrathecal chemotherapy (methotrexate, hydrocortisone, Ara-C) was administered during induction/consolidation.
- Patients were monitored for remission status and survival outcomes.
Main Results:
- Twenty-three of 27 patients (85%) achieved remission by the end of induction/consolidation.
- Event-free survival (EFS) was 0.64 at 12 months for M1 patients at day 35, decreasing to 0.32 by 30-48 months.
- A subgroup with M3 status at day 35 but M1 at day 56 had poor EFS, with all relapsing by 15 months.
- Less than 20% of patients are expected to be alive after 5 years.
Conclusions:
- The intensive chemotherapy regimen achieved high initial remission rates in children with relapsed ALL.
- Long-term event-free survival and overall survival remain limited, highlighting the need for novel therapeutic strategies.
- Prognosis is poor for patients with persistent minimal residual disease (M3) after initial induction therapy.