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      KCI등재 SCI SCIE SCOPUS

      Clinical Prognostic Factors in 86 Chinese Patients with Primary Myelodysplastic Syndromes and Trisomy 8: A Single Institution Experience

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      https://www.riss.kr/link?id=A103610936

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      다국어 초록 (Multilingual Abstract)

      Purpose: The objective was to determine the characteristics and prognostic factors of 86 Chinese patients with trisomy 8 aberrationsand compare the prognostic value of International Prognostic System (IPSS) and Revised IPSS (IPSS-R) in this cohort. M...

      Purpose: The objective was to determine the characteristics and prognostic factors of 86 Chinese patients with trisomy 8 aberrationsand compare the prognostic value of International Prognostic System (IPSS) and Revised IPSS (IPSS-R) in this cohort.
      Materials and Methods: A total of 86 cases diagnosed with primary myelodysplastic syndromes (MDS) with isolated tr8 or with tr8 and other additional cytogenetic aberrations diagnosed and treated at the Union Hospital, Tongji Medical College of Huazhong University of Science and Technology between July 2002 and March 2013 were reviewed.
      Results: The median survival of the entire group was 23.0 months, and acute myeloid leukemia (AML) developed in 43% (37/86) patients within the follow up time. The univariate analysis revealed that overall survival (OS) was correlated with age, thrombocytopenia,absolute neutrophil count, marrow blasts, cytogenetic status and red blood cell transfusion at diagnosis, and the multivariateanalysis revealed that age, marrow blasts, cytogenetic status and transfusion dependence were independent parameters for the OS. The cytogenetic complexity and marrow blasts had the strongest impact on the AML transformation by multivariate analysis. Comparing the two prognostic systems, both two systems could successfully discriminate risk groups for survival. IPSS-R was more refined than IPSS for predicting OS, but had no advantage in predicting the risk of AML development.
      Conclusion: This study confirmed the influence of clinical factors on the prognosis of 86 Chinese MDS patients with trisomy 8. In addition, IPSS-R can further refine prognostic discrimination in the IPSS risk categories.

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      참고문헌 (Reference)

      1 Bernasconi P, "World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes" 137 : 193-205, 2007

      2 Gonzalez Garcia JR, "Use of the International System for Human Cytogenetic Nomenclature (ISCN)" 108 : 3952-3953, 2006

      3 Li L, "Unique cytogenetic features of primary myelodysplastic syndromes in Chinese patients" 33 : 1194-1198, 2009

      4 Xiao Y, "Trisomy 8 is the most frequent cytogenetic abnormality in de novo myelodysplastic syndrome in China" 35 : 100-106, 2012

      5 Paulsson K, "Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes" 55 : 37-48, 2007

      6 Pereira A, "Transfusion intensity, not the cumulative red blood cell transfusion burden, determines the prognosis of patients with myelodysplastic syndrome on chronic transfusion support" 86 : 245-250, 2011

      7 Malcovati L, "Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes" 25 : 3503-3510, 2007

      8 Vardiman JW, "The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia:rationale and important changes" 114 : 937-951, 2009

      9 Al Ameri A, "Significance of thrombocytopenia in myelodysplastic syndromes: associations and prognostic implications" 11 : 237-241, 2011

      10 Greenberg PL, "Revised international prognostic scoring system for myelodysplastic syndromes" 120 : 2454-2465, 2012

      1 Bernasconi P, "World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes" 137 : 193-205, 2007

      2 Gonzalez Garcia JR, "Use of the International System for Human Cytogenetic Nomenclature (ISCN)" 108 : 3952-3953, 2006

      3 Li L, "Unique cytogenetic features of primary myelodysplastic syndromes in Chinese patients" 33 : 1194-1198, 2009

      4 Xiao Y, "Trisomy 8 is the most frequent cytogenetic abnormality in de novo myelodysplastic syndrome in China" 35 : 100-106, 2012

      5 Paulsson K, "Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes" 55 : 37-48, 2007

      6 Pereira A, "Transfusion intensity, not the cumulative red blood cell transfusion burden, determines the prognosis of patients with myelodysplastic syndrome on chronic transfusion support" 86 : 245-250, 2011

      7 Malcovati L, "Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes" 25 : 3503-3510, 2007

      8 Vardiman JW, "The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia:rationale and important changes" 114 : 937-951, 2009

      9 Al Ameri A, "Significance of thrombocytopenia in myelodysplastic syndromes: associations and prognostic implications" 11 : 237-241, 2011

      10 Greenberg PL, "Revised international prognostic scoring system for myelodysplastic syndromes" 120 : 2454-2465, 2012

      11 Ma Y, "Prognostic value of trisomy 8 in primary myelodysplastic syndrome" 40 : 697-703, 2010

      12 Saumell S, "Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes" 159 : 311-321, 2012

      13 Germing U, "Prognostic scoring systems in MDS" 36 : 1463-1469, 2012

      14 Irons RD, "Prevalence of MDS subtypes in Shanghai, China: a comparison of the World Health Organization and French American British classifications" 30 : 769-775, 2006

      15 Sloand EM, "Preferential suppression of trisomy 8 compared with normal hematopoietic cell growth by autologous lymphocytes in patients with trisomy 8 myelodysplastic syndrome" 106 : 841-851, 2005

      16 Wellner JA, "On an exponential bound for the Kaplan-Meier estimator" 13 : 481-496, 2007

      17 Haase D, "New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients" 110 : 4385-4395, 2007

      18 Nolte F, "Myelodysplastic syndromes: molecular pathogenesis and genomic changes" 87 : 777-795, 2008

      19 Greenberg PL, "Myelodysplastic syndromes" 2002 : 136-161, 2002

      20 Nimer SD, "Myelodysplastic syndromes" 111 : 4841-4851, 2008

      21 Gill RD, "Multistate life-tables and regression models" 3 : 259-276, 1992

      22 Greenberg P, "International scoring system for evaluating prognosis in myelodysplastic syndromes" 89 : 2079-2088, 1997

      23 Chun K, "Implementation of standardized international karyotype scoring practices is needed to provide uniform and systematic evaluation for patients with myelodysplastic syndrome using IPSS criteria: An International Working Group on MDS Cytogenetics Study" 34 : 160-165, 2010

      24 Qu S, "Impacts of cytogenetic categories in the Revised International Prognostic Scoring System on the prognosis of primary myelodysplastic syndromes:results of a single-center study" 53 : 940-946, 2012

      25 Malcovati L, "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)" 96 : 1433-1440, 2011

      26 Solé F, "Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes" 90 : 1168-1178, 2005

      27 Olnes MJ, "Directed therapy for patients with myelodysplastic syndromes(MDS) by suppression of cyclin D1 with ON 01910.Na" 36 : 982-989, 2012

      28 Kuendgen A, "Differences in epidemiolo-gy of MDS between Western and Eastern countries: ethnic differences or environmental influence?" 31 : 103-104, 2007

      29 Matsuda A, "Difference in clinical features between Japanese and German patients with refractory anemia in myelodysplastic syndromes" 106 : 2633-2640, 2005

      30 Mufti GJ, "Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts" 93 : 1712-1717, 2008

      31 Pozdnyakova O, "Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities" 113 : 3331-3340, 2008

      32 Lee JJ, "Comparisons of prognostic scoring systems for myelodysplastic syndromes:a Korean multicenter study" 23 : 425-432, 1999

      33 Schanz J, "Coalesced multicentric analysis of 2,351 patients with myelodysplastic syndromes indicates an underestimation of poor-risk cytogenetics of myelodysplastic syndromes in the international prognostic scoring system" 29 : 1963-1970, 2011

      34 Chen B, "Clinical and cytogenetic features of 508 Chinese patients with myelodysplastic syndrome and comparison with those in Western countries" 19 : 767-775, 2005

      35 Cazzola M, "Classification and prognostic evaluation of myelodysplastic syndromes" 38 : 627-634, 2011

      36 Lee JH, "Application of different prognostic scoring systems and comparison of the FAB and WHO classifications in Korean patients with myelodysplastic syndrome" 17 : 305-313, 2003

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