Factors associated with hematopoietic cell transplantation (HCT) among patients in a population-based study of myelodysplastic syndrome (MDS) in Minnesota

被引:0
作者
Angela R. Smith
Erica D. Warlick
Michelle A. Roesler
Jenny N. Poynter
Michaela Richardson
Phuong Nguyen
Adina Cioc
Betsy Hirsch
Julie A. Ross
机构
[1] University of Minnesota,Division of Blood and Marrow Transplantation, Department of Pediatrics
[2] University of Minnesota,Division of Blood and Marrow Transplantation, Department of Medicine
[3] University of Minnesota,Division of Epidemiology and Clinical Research, Department of Pediatrics
[4] University of Minnesota,Masonic Cancer Center
[5] Mayo Clinic,Department of Lab Medicine and Pathology
[6] VA Medical Center Hematopathology,Department of Lab Medicine and Pathology
[7] University of Minnesota,undefined
来源
Annals of Hematology | 2015年 / 94卷
关键词
MDS; Myelodysplastic syndrome; Hematopoietic cell transplantation; Epidemiology;
D O I
暂无
中图分类号
学科分类号
摘要
Myelodysplastic syndrome (MDS) is a clonal hematopoietic stem cell disorder characterized by dysplastic changes in the bone marrow, ineffective erythropoiesis, and an increased risk of developing acute myeloid leukemia. Treatment planning for patients with MDS is a complex process, and we sought to better characterize hematopoietic cell transplantation (HCT) outcomes and the factors that play into decision-making regarding referral of adults with MDS for definitive therapy with HCT. Patients enrolled in a population-based study of MDS between April 2010 and January 2013 who underwent HCT within the first year after enrollment were included in this analysis. Age- and risk-matched MDS patient controls also enrolled during that time period were used as a comparison. Survival was significantly better in the HCT group (48 vs. 21 %, log-rank p value 0.009). Non-HCT patients were more likely to have comorbidities, and HCT patients were more likely to have a college degree and an income >$80,000. All three of these variables were independently associated with HCT, but none impacted survival. Patients with MDS in our study who underwent HCT had better survival than a comparable group of patients who did not undergo HCT. With refined treatment techniques, more patients may be able to be considered for this therapy. More work needs to be done to determine why education and income appear to impact the decision to pursue HCT, but these factors may impact referral to an academic center where aggressive therapy like HCT is more likely to be considered.
引用
收藏
页码:1667 / 1675
页数:8
相关论文
共 110 条
  • [1] Catenacci DV(2005)Myelodysplasic syndromes: a comprehensive review Blood Rev 19 301-319
  • [2] Schiller GJ(2014)Myelodysplastic syndromes: 2014 update on diagnosis, risk-stratification, and management Am J Hematol 89 97-108
  • [3] Garcia-Manero G(2014)Myelodysplastic syndromes Lancet 112 45-52
  • [4] Adès L(2008)Epidemiology of myelodysplastic syndromes and chronic myeloproliferative disorders in the United States, 2001–2004, using data from the NAACCR and SEER programs Blood 120 1686-1694
  • [5] Itzykson R(2014)Underestimation of myelodysplastic syndrome incidence by cancer registries: results from a population-based data linkage study Cancer 114 937-951
  • [6] Fenaux P(2009)The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes Blood 89 2079-2088
  • [7] Rollison DE(1997)International scoring system for evaluating prognosis in myelodysplastic syndromes Blood 120 2454-2465
  • [8] Howlader N(2012)Revised international prognostic scoring system for myelodysplastic syndromes Blood 25 3503-3510
  • [9] Smith MT(2007)Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes J Clin Oncol 96 1433-1440
  • [10] Strom SS(2011)Impact of the degree of anemia on the outcome of patients with myelodysplastic syndrome and its integration into the WHO classification-based Prognostic Scoring System (WPSS) Haematologica 10 223-232