Secondary leukemia following high cumulative doses of etoposide in patients treated for advanced germ cell tumors

J Clin Oncol. 1998 Oct;16(10):3386-91. doi: 10.1200/JCO.1998.16.10.3386.

Abstract

Purpose: High cumulative epipodophyllotoxin dosages are reported to be associated with an elevated risk for secondary acute myeloid leukemia (s-AML). This study examined the risk of s-AML following cumulative etoposide doses greater than 2 g/m2 in patients with metastatic germ cell tumors (GCT).

Patients and methods: The incidence of s-AML was retrospectively assessed in patients treated within clinical trials between January 1986 and February 1996 at four university centers. All patients received high-dose chemotherapy (HDCT) plus autologous stem-cell support for metastatic GCT, including high cumulative etoposide doses (> 2 g/m2). Minimum patient follow-up was 12 months. Standardized morbidity ratio (SMR) was calculated to estimate the risk associated with high cumulative etoposide doses, as compared with the general population.

Results: A total of 302 patients with a median age of 29 years (range, 15 to 55) received a median cumulative etoposide dose of 5 g/m2 (range, 2.4 to 14 g/m2). Four cases of s-AML were observed, which resulted in a cumulative incidence of 1.3% (95% confidence interval [CI], 0.38% to 3.59%) at 52 months of median follow-up (range, 12 to 198). Two cases of secondary myelodysplasia (s-MDS) developed in patients with primary mediastinal GCT. Based on the observed four cases of AML, which are most likely etoposide-related, the risk for developing s-AML (SMR, 160 [95% CI, 43.7 to 411.2]) is significantly increased in comparison to the age-matched general population.

Conclusion: Due to the low incidence of AML in the general population, the significantly elevated risk for developing s-AML affects only 1.3% of all patients who receive etoposide doses greater than 2 g/m2. HDCT, including etoposide doses greater than 2 g/m2, is associated with an acceptably low incidence of s-AML in patients with advanced GCT.

Publication types

  • Multicenter Study

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Antineoplastic Agents, Phytogenic / administration & dosage
  • Antineoplastic Agents, Phytogenic / adverse effects*
  • Drug Administration Schedule
  • Etoposide / administration & dosage
  • Etoposide / adverse effects*
  • Germinoma / drug therapy*
  • Germinoma / secondary
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Leukemia, Monocytic, Acute / chemically induced
  • Leukemia, Myeloid / chemically induced*
  • Leukemia, Myelomonocytic, Acute / chemically induced
  • Male
  • Mediastinal Neoplasms / drug therapy*
  • Middle Aged
  • Myelodysplastic Syndromes / chemically induced
  • Neoplasms, Second Primary / chemically induced*
  • Retroperitoneal Neoplasms / drug therapy*
  • Retrospective Studies
  • Testicular Neoplasms / drug therapy*

Substances

  • Antineoplastic Agents, Phytogenic
  • Etoposide