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Volumn 193, Issue 2, 2009, Pages 78-85

Does MDS with der(1;7)(q10;p10) constitute a distinct risk group? A retrospective single institutional analysis of clinical/pathologic features compared to -7/del(7q) MDS

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ADULT; AGE DISTRIBUTION; AGED; ARTICLE; BLAST CELL; CHILD; CHROMOSOME 1Q; CHROMOSOME 7P; CHROMOSOME 7Q; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 7; CLINICAL FEATURE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; HUMAN; MAJOR CLINICAL STUDY; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; RISK ASSESSMENT; SURVIVAL RATE; SURVIVAL TIME; THROMBOCYTE COUNT;

EID: 68149160596     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2009.04.013     Document Type: Article
Times cited : (19)

References (30)
  • 4
    • 33644746245 scopus 로고    scopus 로고
    • Additional cytogenetic changes and previous genotoxic exposure predict unfavorable prognosis in myelodysplastic syndromes and acute myeloid leukemia with der(1;7)(q10;p10)
    • Hsiao H.H., Sashida G., Ito Y., Kodama A., Fukutake K., Ohyashiki J.H., and Ohyashiki K. Additional cytogenetic changes and previous genotoxic exposure predict unfavorable prognosis in myelodysplastic syndromes and acute myeloid leukemia with der(1;7)(q10;p10). Cancer Genet Cytogenet 165 (2006) 161-166
    • (2006) Cancer Genet Cytogenet , vol.165 , pp. 161-166
    • Hsiao, H.H.1    Sashida, G.2    Ito, Y.3    Kodama, A.4    Fukutake, K.5    Ohyashiki, J.H.6    Ohyashiki, K.7
  • 7
    • 40749102056 scopus 로고    scopus 로고
    • Clinicopathological features of unbalanced translocation Der(1;7)(q10;p10) in myeloid neoplasms
    • So C.C., Ma E.S., Wan T.S., Yip S.F., and Chan L.C. Clinicopathological features of unbalanced translocation Der(1;7)(q10;p10) in myeloid neoplasms. Leuk Res 32 (2008) 1000-1001
    • (2008) Leuk Res , vol.32 , pp. 1000-1001
    • So, C.C.1    Ma, E.S.2    Wan, T.S.3    Yip, S.F.4    Chan, L.C.5
  • 12
    • 4444302228 scopus 로고    scopus 로고
    • Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation
    • Christiansen D.H., Andersen M.K., and Pedersen-Bjergaard J. Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation. Blood 104 (2004) 1474-1481
    • (2004) Blood , vol.104 , pp. 1474-1481
    • Christiansen, D.H.1    Andersen, M.K.2    Pedersen-Bjergaard, J.3
  • 13
    • 1542373639 scopus 로고    scopus 로고
    • High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
    • Harada H., Harada Y., Niimi H., Kyo T., Kimura A., and Inaba T. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood 103 (2004) 2316-2324
    • (2004) Blood , vol.103 , pp. 2316-2324
    • Harada, H.1    Harada, Y.2    Niimi, H.3    Kyo, T.4    Kimura, A.5    Inaba, T.6
  • 15
    • 28544448340 scopus 로고    scopus 로고
    • Mutations of genes in the receptor tyrosine kinase (RTK)/RAS-BRAF signal transduction pathway in therapy-related myelodysplasia and acute myeloid leukemia
    • Christiansen D.H., Andersen M.K., Desta F., and Pedersen-Bjergaard J. Mutations of genes in the receptor tyrosine kinase (RTK)/RAS-BRAF signal transduction pathway in therapy-related myelodysplasia and acute myeloid leukemia. Leukemia 19 (2005) 2232-2240
    • (2005) Leukemia , vol.19 , pp. 2232-2240
    • Christiansen, D.H.1    Andersen, M.K.2    Desta, F.3    Pedersen-Bjergaard, J.4
  • 16
    • 0029020637 scopus 로고
    • Refractory cytopenia with t(1;7),+8 abnormality and dysplastic eosinophils showing intranuclear Charcot-Leyden crystals: a fluorescence in situ hybridization study
    • Ma S.K., Wong K.F., Chan J.K., and Kwong Y.L. Refractory cytopenia with t(1;7),+8 abnormality and dysplastic eosinophils showing intranuclear Charcot-Leyden crystals: a fluorescence in situ hybridization study. Br J Haematol 90 (1995) 216-218
    • (1995) Br J Haematol , vol.90 , pp. 216-218
    • Ma, S.K.1    Wong, K.F.2    Chan, J.K.3    Kwong, Y.L.4
  • 18
    • 18744423188 scopus 로고    scopus 로고
    • Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization
    • Forrest D.L., Horsman D.E., Jensen C.L., Berry B.R., Dalal B.I., Barnett M.J., and Nantel S.H. Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization. Cancer Genet Cytogenet 107 (1998) 65-68
    • (1998) Cancer Genet Cytogenet , vol.107 , pp. 65-68
    • Forrest, D.L.1    Horsman, D.E.2    Jensen, C.L.3    Berry, B.R.4    Dalal, B.I.5    Barnett, M.J.6    Nantel, S.H.7
  • 21
    • 57649119892 scopus 로고    scopus 로고
    • 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
    • Pozdnyakova O., Miron P.M., Tang G., Walter O., Raza A., Woda B., and Wang S.A. 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. Cancer 113 (2008) 3331-3340
    • (2008) Cancer , vol.113 , pp. 3331-3340
    • Pozdnyakova, O.1    Miron, P.M.2    Tang, G.3    Walter, O.4    Raza, A.5    Woda, B.6    Wang, S.A.7
  • 22
    • 0037081847 scopus 로고    scopus 로고
    • Predominance of trisomy 1q in myelodysplastic syndromes in Korea: is there an ethnic difference? A 3-year multi-center study
    • Lee D.S., Kim S.H., Seo E.J., Park C.J., Chi H.S., Ko E.K., Yoon B.H., Kim W.H., and Cho H.I. Predominance of trisomy 1q in myelodysplastic syndromes in Korea: is there an ethnic difference? A 3-year multi-center study. Cancer Genet Cytogenet 132 (2002) 97-101
    • (2002) Cancer Genet Cytogenet , vol.132 , pp. 97-101
    • Lee, D.S.1    Kim, S.H.2    Seo, E.J.3    Park, C.J.4    Chi, H.S.5    Ko, E.K.6    Yoon, B.H.7    Kim, W.H.8    Cho, H.I.9
  • 23
    • 33847132734 scopus 로고    scopus 로고
    • Loss of 17p is a major consequence of whole-arm chromosome translocations in hematologic malignancies
    • Adeyinka A., Wei S., and Sanchez J. Loss of 17p is a major consequence of whole-arm chromosome translocations in hematologic malignancies. Cancer Genet Cytogenet 173 (2007) 136-143
    • (2007) Cancer Genet Cytogenet , vol.173 , pp. 136-143
    • Adeyinka, A.1    Wei, S.2    Sanchez, J.3
  • 27
    • 38949123096 scopus 로고    scopus 로고
    • Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML
    • Gondek L.P., Tiu R., O'Keefe C.L., Sekeres M.A., Theil K.S., and Maciejewski J.P. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. Blood 111 (2008) 1534-1542
    • (2008) Blood , vol.111 , pp. 1534-1542
    • Gondek, L.P.1    Tiu, R.2    O'Keefe, C.L.3    Sekeres, M.A.4    Theil, K.S.5    Maciejewski, J.P.6
  • 28
  • 30
    • 48749111872 scopus 로고    scopus 로고
    • Molecular pathways in myelodysplastic syndromes and acute myeloid leukemia: relationships and distinctions-a review
    • Bernasconi P. Molecular pathways in myelodysplastic syndromes and acute myeloid leukemia: relationships and distinctions-a review. Br J Haematol 142 (2008) 695-708
    • (2008) Br J Haematol , vol.142 , pp. 695-708
    • Bernasconi, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.