High frequency of etoposide (VP-16)-related secondary leukemia in children with non-Hodgkin's lymphoma.

Abstract

PATIENTS AND METHODS:

We report patients who were treated for non-Hodgkin's lymphoma (NHL) or Ki-1 antigen-positive (Ki-1) lymphoma with a T-8801 protocol that included etoposide (VP-16) and behenoylcytosine arabinoside.

RESULTS:

Secondary acute myeloid leukemia (AML) developed in 5 of 38 NHL and Ki-1 lymphoma patients, and the cumulative risk at 4 years was 18.4%. The median time from the initiation of the chemotherapy to the development of AML was 21 months (range, 13-30). Four patients had a FAB M5 morphology, and one had FAB M2. In four of five examined cases, chromosomal alterations involving the long arm of chromosome 11 were demonstrated at the time of development of AML. None of the 46 NHL patients who we treated with another protocol (B-8801), using significantly higher cumulative doses of VP-16 than in the case of the patients with T-8801 and a different schedule of VP-16 administration, developed secondary AML.

CONCLUSIONS:

The risk of secondary AML possibly related to the use of VP-16 given twice weekly.

• Authors: K Sugita, T Furukawa, M Tsuchida, Y Okawa, S Nakazawa, J Akatsuka, M Ohira, K Nishimura
• Journal: The American journal of pediatric hematology/oncology (Am J Pediatr Hematol Oncol) Vol. 15 Issue 1 Pg. 99-104 (Feb 1993) ISSN: 0192-8562 [Print] United States
• PMID: 8447565 (Publication Type: Case Reports, Comparative Study, Journal Article)

Chemical References

• Cytarabine
• Vincristine
• Etoposide
• Asparagine
• Doxorubicin
• Cyclophosphamide
• Mercaptopurine
• Methotrexate

Topics

• Adolescent
• Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
• Asparagine (administration & dosage)
• Child
• Child, Preschool
• Chromosome Aberrations
• Chromosomes, Human, Pair 11 (ultrastructure)
• Cyclophosphamide (administration & dosage)
• Cytarabine (administration & dosage)
• Doxorubicin (administration & dosage)
• Etoposide (administration & dosage, adverse effects)
• Female
• Follow-Up Studies
• Humans
• Leukemia, Monocytic, Acute (chemically induced, epidemiology)
• Leukemia, Myeloid, Acute (chemically induced, epidemiology)
• Life Tables
• Lymphoma, Non-Hodgkin (drug therapy)
• Male
• Mercaptopurine (administration & dosage)
• Methotrexate (administration & dosage)
• Neoplasms, Second Primary (chemically induced, epidemiology)
• Risk
• Vincristine (administration & dosage)