Comparison of risk stratification tools in predicting outcomes of patients with higher-risk myelodysplastic syndromes treated with azanucleosides

被引:0
|
作者
A M Zeidan
M A Sekeres
G Garcia-Manero
D P Steensma
K Zell
J Barnard
N A Ali
C Zimmerman
G Roboz
A DeZern
A Nazha
E Jabbour
H Kantarjian
S D Gore
J P Maciejewski
A List
R Komrokji
机构
[1] Section of Hematology,Department of Internal Medicine
[2] Yale Comprehensive Cancer Center,Department of Translational Hematology and Oncology Research
[3] Yale University,Department of leukemia
[4] Leukemia Program,Department of Medical Oncology
[5] Cleveland Clinic,Department of Malignant Hematology
[6] MD Anderson Cancer Center,Department of Medicine
[7] Dana-Farber Cancer Institute,Department of Medicine
[8] H. Lee Moffitt Cancer Center and Research Institute,undefined
[9] Weill Medical College of Cornell University,undefined
[10] Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University,undefined
来源
Leukemia | 2016年 / 30卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Established prognostic tools in patients with myelodysplastic syndromes (MDS) were largely derived from untreated patient cohorts. Although azanucleosides are standard therapies for higher-risk (HR)-MDS, the relative prognostic performance of existing prognostic tools among patients with HR-MDS receiving azanucleoside therapy is unknown. In the MDS Clinical Research Consortium database, we compared the prognostic utility of the International Prognostic Scoring System (IPSS), revised IPSS (IPSS-R), MD Anderson Prognostic Scoring System (MDAPSS), World Health Organization-based Prognostic Scoring System (WPSS) and the French Prognostic Scoring System (FPSS) among 632 patients who presented with HR-MDS and were treated with azanucleosides as the first-line therapy. Median follow-up from diagnosis was 15.7 months. No prognostic tool predicted the probability of achieving an objective response. Nonetheless, all five tools were associated with overall survival (OS, P=0.025 for the IPSS, P=0.011 for WPSS and P<0.001 for the other three tools). The corrected Akaike Information Criteria, which were used to compare OS with the different prognostic scoring systems as covariates (lower is better) were 4138 (MDAPSS), 4156 (FPSS), 4196 (IPSS-R), 4186 (WPSS) and 4196 (IPSS). Patients in the highest-risk groups of the prognostic tools had a median OS from diagnosis of 11−16 months and should be considered for up-front transplantation or experimental approaches.
引用
收藏
页码:649 / 657
页数:8
相关论文
共 50 条
  • [21] Clinical impact of transformation to acute myeloid leukemia in patients with higher-risk myelodysplastic syndromes
    Kota, Vamsi
    Ogbonnaya, Augustina
    Farrelly, Eileen
    Schroader, Bridgette Kanz
    Raju, Aditya
    Kristo, Fjoralba
    Dalal, Mehul
    FUTURE ONCOLOGY, 2022, 18 (36) : 4017 - 4029
  • [22] Demonstration of additional benefit in adding lenalidomide to azacitidine in patients with higher-risk myelodysplastic syndromes
    Sekeres, Mikkael A.
    O'Keefe, Christine
    List, Alan F.
    Paulic, Katarina
    Afable, Manuel, II
    Englehaupt, Ricki
    Maciejewski, Jaroslaw P.
    AMERICAN JOURNAL OF HEMATOLOGY, 2011, 86 (01) : 102 - 103
  • [23] Predictors of hypomethylating agent discontinuation among patients with higher-risk myelodysplastic syndromes.
    Zeidan, Amer Methqal
    Joshi, Namita
    Kale, Hrishikesh
    Wang, Wei-Jhih
    Corman, Shelby
    Hill, Kala
    Salimi, Tehseen
    Epstein, Robert S.
    JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (15)
  • [24] Gene methylation and cytogenetic abnormalities in patients (pts) with higher-risk myelodysplastic syndromes.
    Mufti, G. J.
    Herman, J. G.
    Gore, S.
    Seymour, J. F.
    Santini, V.
    Hagemeijer, A. M.
    Skikne, B.
    MacBeth, K. J.
    Lucy, L. M.
    Beach, C. L.
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [25] Phase 2 study of the lenalidomide and azacitidine combination in patients with higher-risk myelodysplastic syndromes
    Sekeres, Mikkael A.
    Tiu, Ramon V.
    Komrokji, Rami
    Lancet, Jeffrey
    Advani, Anjali S.
    Afable, Manuel
    Englehaupt, Ricki
    Juersivich, Joyce
    Cuthbertson, David
    Paleveda, Jennifer
    Tabarroki, Ali
    Visconte, Valeria
    Makishima, Hideki
    Jerez, Andres
    Paquette, Ronald
    List, Alan F.
    Maciejewski, Jaroslaw P.
    BLOOD, 2012, 120 (25) : 4945 - 4951
  • [26] Efficacy, safety, and pharmacokinetics of subcutaneous azacitidine in Taiwanese patients with higher-risk myelodysplastic syndromes
    Chou, Wen-Chien
    Yeh, Su-Peng
    Hsiao, Liang-Tsai
    Lin, Sheng-Fung
    Chen, Yeu-Chin
    Chen, Tsai-Yun
    Laille, Eric
    Galettis, Anoula
    Dong, Qian
    Songer, Steve
    Beach, C. L.
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2017, 13 (05) : E430 - E439
  • [27] Enhancing our chances of picking a winner in higher-risk myelodysplastic syndromes
    Wei, Andrew H.
    Seymour, John F.
    BRITISH JOURNAL OF HAEMATOLOGY, 2022, 198 (03) : 415 - 418
  • [28] Treatment of Higher-Risk Myelodysplastic Syndromes After Failure of Hypomethylating Agents
    Komrokji, Rami S.
    CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2015, 15 : S56 - S59
  • [29] Azacitidine and Venetoclax Combination for Upfront Treatment of Higher-Risk Myelodysplastic Syndromes
    Al Ali, Najla
    Sallman, David
    Chan, Onyee
    Padron, Eric
    Sweet, Kendra
    Kuykendall, Andrew
    Lancet, Jeffrey
    Komrokji, Rami
    CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2021, 21 : S341 - S341
  • [30] Systematic Literature Review of Treatment Options and Clinical Outcomes for Patients With Higher-Risk Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia
    Bell, Jill A.
    Galaznik, Aaron
    Huelin, Rachel
    Stokes, Michael
    Guo, Yelan
    Fram, Robert J.
    Faller, Douglas V.
    CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2018, 18 (04): : E157 - E166