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Prolymphocytic leukemia. Response to asparaginase
Archives of Internal Medicine
|January 1, 1981
Summary
Asparaginase offers a dramatic response in prolymphocytic leukemia of the null cell type, significantly reducing lymphocyte counts. This finding suggests asparaginase as a potential initial therapy for this leukemia subtype.
Area of Science:
- Hematology
- Oncology
Background:
- Chronic lymphocytic leukemia (CLL) patient presented with a high lymphocyte count.
- Diagnosis confirmed as prolymphocytic leukemia of the null cell type based on morphology and surface markers.
Observation:
- The leukemia was refractory to standard treatments including alkylating agents, combination chemotherapy, and leukapheresis.
- Initial therapy with prednisone and vincristine sulfate showed no significant effect.
Findings:
- Addition of asparaginase to prednisone and vincristine sulfate resulted in a rapid and dramatic response.
- Peripheral lymphocyte count decreased from 980 X 10(9)/L to 20 X 10(9)/L within two weeks.
- Restoration of polymorphonuclear leukocyte concentration towards normal levels was observed.
Implications:
- Asparaginase demonstrates significant efficacy in a treatment-resistant case of prolymphocytic leukemia.
- Suggests considering asparaginase as an initial induction therapy for prolymphocytic leukemia of the null cell type.
- Highlights a potential new therapeutic strategy for this rare leukemia subtype.