Therapy-related leukemia and myelodysplastic syndrome in breast cancer patients treated with cyclophosphamide or anthracyclines

Jpn J Clin Oncol. 1999 Jan;29(1):28-32. doi: 10.1093/jjco/29.1.28.

Abstract

Background: Accumulation of data regarding therapy-related leukemia (TRL) or myelodysplastic syndrome (t-MDS) is critical for assessing the risk of developing such diseases and for subsequent decision-making processes for better treatment.

Methods: We evaluated the clinical characteristics of patients with TRL/t-MDS diagnosed at the National Cancer Center Hospital between January 1989 and September 1997. This report is concerned with those patients who initially had been treated with chemotherapeutic agents for breast cancer.

Results: Thirteen patients (median age, 55 years) developed TRL (n = 4) or t-MDS (n = 9). The median interval between the development of TRL/t-MDS and initial treatment was 94 months (range 23-190 months). For the primary therapy, all patients had received intense and prolonged treatment with cyclophosphamide (CPA) and/or anthracyclines including doxorubicin (DOX), with a median cumulative dose of 55 g/body (range 16.4-288.5 g) for CPA and 480 mg/m2 (range 395-625.5 mg/m2) for DOX. Seven patients were subsequently treated by chemotherapy and one received an allogeneic bone marrow transplantation.

Conclusions: Clinicians must remain alert to the risks associated with unproven medical practices which include long-term administration of alkylating agents. Selected patients with TRL/t-MDS may respond to intense salvage combination chemotherapy.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents, Alkylating / adverse effects*
  • Breast Neoplasms / drug therapy*
  • Cyclophosphamide / adverse effects*
  • Doxorubicin / adverse effects*
  • Female
  • Humans
  • Leukemia / chemically induced*
  • Middle Aged
  • Myelodysplastic Syndromes / chemically induced*
  • Neoplasms, Second Primary / chemically induced*

Substances

  • Antineoplastic Agents
  • Antineoplastic Agents, Alkylating
  • Doxorubicin
  • Cyclophosphamide