Outcome of patients with myelodysplastic syndromes in the Veterans Administration population

Rami S Komrokji1, Gina M Matacia-Murphy, Najla H Al Ali

  • 1Department of Hematologic Malignancies, H. Lee Moffitt Cancer and Research Institute, Tampa, FL 33612, USA. rami.komrokji@moffitt.org

Leukemia Research
|April 17, 2009
PubMed
Abstract

Insights

This study analyzed myelodysplastic syndromes (MDS) in US veterans, finding outcomes similar to national data. Improved registry coding is recommended for better comparisons of MDS patient outcomes.

Area of Science:

  • Hematology
  • Oncology
  • Epidemiology

Background:

  • Myelodysplastic syndromes (MDS) epidemiology and outcomes in the United States require further characterization.
  • The Surveillance, Epidemiology, and End Results (SEER) Program began reporting MDS in 2001.
  • This study presents the first analysis of MDS within the large Veteran Affairs (VA) system.

Purpose of the Study:

  • To investigate the epidemiology and outcomes of myelodysplastic syndromes (MDS) in a large population of US veterans.
  • To establish a baseline understanding of MDS within the VA healthcare system.

Main Methods:

  • Utilized the VA Central Cancer Registry (VACCR) data from 1995-2006.
  • Identified 2242 cases of MDS using ICD-03 histology codes across 127 VA Medical Centers.
  • Analyzed overall survival (OS) based on French-American-British (FAB) classification.

Main Results:

  • A total of 2242 MDS cases were identified between 1995 and 2006.
  • The median overall survival (OS) for MDS patients was 2.1 years.
  • Median OS varied significantly by FAB subtype: RA (3.4 years), RARS (4.9 years), and RAEB (0.7 years). No OS differences were noted based on race.

Conclusions:

  • Outcomes for MDS patients in the VA system align with existing literature and SEER Program data.
  • Enhanced coding for World Health Organization (WHO) subtypes, International Prognostic Scoring System (IPSS), and treatment details in MDS registries is crucial.
  • Standardized data collection will facilitate more robust comparisons of MDS outcomes across diverse patient populations.