Abstract |
We studied the impact of etoposide on the prognosis of 81 patients (77 of whom were children <15 years old) with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis (EBV-HLH). The study group received a median cumulative dose of 1,500 mg/m2 etoposide (range, 0-14,550 mg/m2), with a median follow-up period of 44 months (range, 20-88 months) from the diagnosis. Only 1 patient, who received 3150 mg/m2 etoposide, developed therapy-related acute myeloid leukemia (t-AML), at 31 months after diagnosis. Excluding 9 patients who underwent hemopoietic stem cell transplantation during the course of treatment, the prognosis was poorer for those patients who received less than a 1,000 mg/m2 cumulative dose of etoposide. Our results indicate that the risk of etoposide-related t-AML is low. An appropriate dosage of etoposide for the treatment of EBV-HLH would be in the range of 1,000 to 3,000 mg/m2. However, even at these doses, care must be taken to prevent the rare risk of t-AML.
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Authors | Shinsaku Imashuku, Tomoko Teramura, Kikuko Kuriyama, Junichi Kitazawa, Etsuro Ito, Akira Morimoto, Shigeyoshi Hibi |
Journal | International journal of hematology
(Int J Hematol)
Vol. 75
Issue 2
Pg. 174-7
(Feb 2002)
ISSN: 0925-5710 [Print] Japan |
PMID | 11939264
(Publication Type: Clinical Trial, Journal Article, Multicenter Study)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Etoposide
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Topics |
- Acute Disease
- Adolescent
- Adult
- Antineoplastic Agents, Phytogenic
(administration & dosage, toxicity)
- Child
- Child, Preschool
- Epstein-Barr Virus Infections
(complications, drug therapy)
- Etoposide
(administration & dosage, toxicity)
- Female
- Follow-Up Studies
- Histiocytosis, Non-Langerhans-Cell
(complications, drug therapy, virology)
- Humans
- Infant
- Leukemia, Myeloid
(chemically induced)
- Male
- Neoplasms, Second Primary
(chemically induced)
- Risk Assessment
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