Chemotherapy-related - late occurring - Philadelphia chromosome in AML, ALL and CML. Similar events related to treatment with DNA topoisomerase II inhibitors?

Leukemia. 1997 Sep;11(9):1571-4. doi: 10.1038/sj.leu.2400769.

Abstract

Therapy with DNA topoisomerase II inhibitors has been shown to result in an increased risk of acute myeloid leukemia (AML), often presenting balanced translocations to chromosome bands 11q23 and 21q22. Also other balanced aberrations, more rarely observed in therapy-related AML (t-AML), such as t(15;17) and inv(16) have been associated with these drugs. Recently we observed a case of chronic myeloid leukemia (CML) with t(9;22) after therapy of a germ cell tumor with etoposide, cisplatin and bleomycin. Based on this case and a review of chemotherapy-related leukemias with t(9;22) from the literature, we suggest a causal relationship between therapy with DNA topoisomerase II inhibitors and development of various types of leukemia carrying the Philadelphia chromosome.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Agents, Phytogenic / adverse effects
  • Child
  • Child, Preschool
  • Doxorubicin / adverse effects
  • Enzyme Inhibitors / adverse effects*
  • Etoposide / adverse effects
  • Female
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / chemically induced*
  • Leukemia, Myeloid, Acute / chemically induced*
  • Male
  • Neoplasms, Second Primary*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / chemically induced*
  • Topoisomerase II Inhibitors*

Substances

  • Antineoplastic Agents, Phytogenic
  • Enzyme Inhibitors
  • Topoisomerase II Inhibitors
  • Etoposide
  • Doxorubicin