Prognosis of patients with intermediate risk IPSS-R myelodysplastic syndrome indicates variable outcomes and need for models beyond IPSS-R

被引:31
作者
Benton, Christopher B. [1 ]
Khan, Maliha [1 ]
Sallman, David [2 ]
Nazha, Aziz [3 ]
Gonzalez, Graciela M. Nogueras [4 ]
Piao, Jin [4 ]
Ning, Jing [4 ]
Aung, Fleur [5 ]
Al Ali, Najla [2 ]
Jabbour, Elias [1 ]
Kadia, Tapan M. [1 ]
Borthakur, Gautam [1 ]
Ravandi, Farhad [1 ]
Pierce, Sherry [1 ]
Steensma, David [6 ]
DeZern, Amy [7 ]
Roboz, Gail [8 ]
Sekeres, Mikkael [3 ]
Andreeff, Michael [1 ]
Kantarjian, Hagop [1 ]
Komrokji, Rami S. [2 ]
Garcia-Manero, Guillermo [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, 1515 Holcombe Blvd Unit 428, Houston, TX 77030 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Malignant Hematol, Tampa, FL USA
[3] Cleveland Clin, Dept Leukemia, Cleveland, OH 44106 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Stat, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Lab Med, Houston, TX 77030 USA
[6] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[7] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[8] Weill Cornell Med, Joan & Sanford I Weill Dept Med, New York, NY USA
关键词
ACUTE MYELOID-LEUKEMIA; SCORING SYSTEM; REGRESSION-MODELS; RESPONSE CRITERIA; SURVIVAL; MDS; BETA-2-MICROGLOBULIN; STRATIFICATION; CLASSIFICATION; TRANSFORMATION;
D O I
10.1002/ajh.25234
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The International Prognostic Scoring System-Revised (IPSS-R) is one standard for myelodysplastic syndrome (MDS) risk stratification. It divides patients into five categories including an intermediate subset (IPSS-R int-risk). Outcomes and clinical interventions for patients with IPSS-R int-risk are not well defined. We performed an analysis of outcomes of this group of patients. Out of 3167 patients, a total of 298 were identified with IPSS-R int-risk MDS and retrospectively analyzed to assess characteristics affecting outcomes. Cox proportional hazard models for overall survival (OS) were performed to identify statistically significant clinical factors that influence survival. Age of 66 years or greater, peripheral blood blasts of 2% or more, and history of red blood cell (RBC) transfusion were significantly associated with inferior survival. Based on these features, MDS patients with IPSS-R int-risk were classified into two prognostic risk groups for analysis, an int-favorable group and an int-adverse group, and had significantly divergent outcomes. Sequential prognostication was validated using two independent datasets comprising over 700 IPSS-R int-risk patients. The difference in median survival between int-favorable and int-adverse patients was 3.7 years in the test cohort, and 1.8 and 2.0 years in the two validation cohorts. These results confirm significantly variable outcomes of patients with IPSS-R int-risk and need for different prognostic systems.
引用
收藏
页码:1245 / 1253
页数:9
相关论文
共 33 条
  • [1] Having a higher blast percentage in circulation than bone marrow: clinical implications in myelodysplastic syndrome and acute lymphoid and myeloid leukemias
    Amin, HM
    Yang, Y
    Shen, Y
    Estey, EH
    Giles, FJ
    Pierce, SA
    Kantarjian, HM
    O'Brien, SM
    Jilani, I
    Albitar, M
    [J]. LEUKEMIA, 2005, 19 (09) : 1567 - 1572
  • [2] The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia
    Arber, Daniel A.
    Orazi, Attilio
    Hasserjian, Robert
    Thiele, Jurgen
    Borowitz, Michael J.
    Le Beau, Michelle M.
    Bloomfield, Clara D.
    Cazzola, Mario
    Vardiman, James W.
    [J]. BLOOD, 2016, 127 (20) : 2391 - 2405
  • [3] Clinical Effect of Point Mutations in Myelodysplastic Syndromes
    Bejar, Rafael
    Stevenson, Kristen
    Abdel-Wahab, Omar
    Galili, Naomi
    Nilsson, Bjoern
    Garcia-Manero, Guillermo
    Kantarjian, Hagop
    Raza, Azra
    Levine, Ross L.
    Neuberg, Donna
    Ebert, Benjamin L.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) : 2496 - 2506
  • [4] Circulating myeloid colony-forming cells predict survival in myelodysplastic syndromes
    Berer, A
    Jäger, E
    Sagaster, V
    Streubel, B
    Wimazal, F
    Sperr, WR
    Welterman, A
    Schwarzinger, I
    Frommlet, F
    Haas, OA
    Valent, P
    Lechner, K
    Geissler, K
    Öhler, L
    [J]. ANNALS OF HEMATOLOGY, 2003, 82 (05) : 271 - 277
  • [5] Prognostic index for adult patients with acute myeloid leukemia in first relapse
    Breems, DA
    Van Putten, WLJ
    Huijgens, PC
    Ossenkoppele, GJ
    Verhoef, GEG
    Verdonck, LF
    Vellenga, E
    De Greef, G
    Jacky, E
    Van der Lelie, J
    Boogaerts, MA
    Löwenberg, B
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (09) : 1969 - 1978
  • [6] Myelodysplastic syndromes - Coping with ineffective hematopoiesis
    Cazzola, M
    Malcovati, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (06) : 536 - 538
  • [7] Cheson BD, 2000, BLOOD, V96, P3671
  • [8] COX DR, 1972, J R STAT SOC B, V34, P187
  • [9] Five-group cytogenetic risk classification, monosomal karyotype, and outcome after hematopoietic cell transplantation for MDS or acute leukemia evolving from MDS
    Deeg, H. Joachim
    Scott, Bart L.
    Fang, Min
    Shulman, Howard M.
    Gyurkocza, Boglarka
    Myerson, David
    Pagel, John M.
    Platzbecker, Uwe
    Ramakrishnan, Aravind
    Radich, Jerald P.
    Sandmaier, Brenda M.
    Sorror, Mohamed
    Stirewalt, Derek L.
    Wilson, Wendy A.
    Storb, Rainer
    Appelbaum, Frederick R.
    Gooley, Ted
    [J]. BLOOD, 2012, 120 (07) : 1398 - 1408
  • [10] Augmented Backward Elimination: A Pragmatic and Purposeful Way to Develop Statistical Models
    Dunkler, Daniela
    Plischke, Max
    Leffondre, Karen
    Heinze, Georg
    [J]. PLOS ONE, 2014, 9 (11):