Therapy-related leukemia and myelodysplastic syndrome in chronic lymphocytic leukemia

L. E. Robertson, Elihu Estey, Hagop Kantarjian, Charles Koller, Susan O'Brien, Barry Brown, Michael J. Keating

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

A retrospective analysis was performed to determine the incidence and clinical features of acute myelogenous leukemia/myelodysplastic syndrome (AML/MDS) developing in chronic lymphocytic leukemia (CLL) patients. AML/MDS occurred in 3/1374 CLL patients seen at a single institution between 1972 and 1992. The median follow-up exceeded 7 years and 72% of these patients had received prior alkylating agent therapy. The expected number of AML/MDS developing in a general population of the same size was 1.2 as calculated from the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) Program data (observed-to-expected ratio = 2.49; 95% confidence interval = 0.9-7.3; p = 0.12). Although, not included in the incidence calculation, four patients with CLL were referred at the time of development of AML/MDS. CLL and AML/MDS were diagnosed concurrently in two patients. Three of the patients had received no prior alkylating agents. The median survival was 17 months in patients who had received no prior treatment, and 5 months in those who had received prior chemotherapy. Our results suggest that patients with CLL in whom AML/MDS develops have similar prognoses to other patients with AML/MDS. Furthermore, this analysis does not provide evidence for a heightened risk of AML/MDS in CLL patients, despite treatment with known leukemogenic agents.

Original languageEnglish (US)
Pages (from-to)2047-2051
Number of pages5
JournalLeukemia
Volume8
Issue number12
StatePublished - Dec 1994

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Therapy-related leukemia and myelodysplastic syndrome in chronic lymphocytic leukemia'. Together they form a unique fingerprint.

Cite this