Gain of 1q in pediatric myelodysplastic syndromes

Leukemia Research

Volumn 30, Issue 11, 2006, Pages 1437-1441

  Morerio, Cristina ^a   Rapella, Annamaria ^a   Tassano, Elisa ^a   Lanino, Edoardo ^a   Micalizzi, Concetta ^a   Rosanda, Cristina ^a   Panarello, Claudio ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

Childhood myelodysplastic syndrome; Cytogenetic abnormalities; Gain of 1q; Prognostic groups

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BLOOD TRANSFUSION; CHILD; CHROMOSOME 1Q; CHROMOSOME 6; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CYTOGENETICS; FEMALE; HEMATOPOIETIC CELL; HUMAN; KARYOTYPE; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; PROGNOSIS;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 6; FATAL OUTCOME; FEMALE; HUMANS; KARYOTYPING; MALE; MYELODYSPLASTIC SYNDROMES; TRANSLOCATION, GENETIC; TRISOMY;

EID: 33748105656     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2005.12.022     Document Type: Article

References (27)

1. Hasle H., Niemeyer C.M., Chessells J.M., Baumann I., Bennett J.M., Kerndrup G., et al. A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases. Leukemia 17 (2003) 277-282
2. Haase D., Fonatsch C., Freund M., Wormann B., Bodenstein H., Bartels H., et al. Cytogenetic findings in 179 patients with myelodysplastic syndromes. Ann Hematol 70 (1995) 171-187
3. Steidl C., Steffens R., Gassmann W., Hildebrandt B., Hilgers R., Germing U., et al. Adequate cytogenetic examination in myelodysplastic syndromes: analysis of 529 patients. Leuk Res 29 (2005) 987-993
4. Horiike S., Taniwaki M., Misawa S., Nishigaki H., Okuda T., Yokota S., et al. The unbalanced 1;7 translocation in de novo myelodysplastic syndrome and its clinical implication. Cancer 65 (1990) 1350-1354
5. Hamamoto K., Hashimoto-Ninomiya A., Kishimoto Y., Kimura T., Fujitake H., Yasunaga K., et al. Unbalanced 1;7 translocation in myelodysplastic syndrome following treatment of acute myeloblastic leukemia with an 8;21 translocation. Cancer Genet Cytogenet 74 (1994) 35-39
6. Lee D.S., Kim S.H., Seo E.J., Park C.J., Chi H.S., Ko E.K., et al. 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
7. Mathews S., Head D., Rodriguez-Galindo C., and Raimondi S.C. Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor. Leuk Lymphoma 37 (2000) 213-218
8. Horsman D.E., Massing B.G., Chan K.W., and Kalousek D.K. Unbalanced translocation (1;7) in childhood myelodysplasia. Am J Hematol 27 (1988) 174-178
9. Fonatsch C., Haase D., Freund M., Bartels H., and Tesch H. Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes?. Cancer Genet Cytogenet 56 (1991) 243-253
10. Hasle H., Baumann I., Bergstrasser E., Fenu S., Fischer A., Kardos G., et al., European Working Group on Childhood MDS. The International Prognostic Scoring System (IPSS) for childhood myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML). Leukemia 18 (2004) 2008-2014
11. Greenberg P., Cox C., LeBeau M.M., Fenaux P., Morel P., Sanz G., et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 89 (1997) 2079-2088
12. Scheres J.M., Hustinx T.W., Geraedts J.P., Leeksma C.H., and Meltzer P.S. Translocation 1;7 in hematologic disorders: a brief review of 22 cases. Cancer Genet Cytogenet 18 (1985) 207-213
13. Yunis J.J., Rydell R.E., Oken M.M., Arnesen M.A., Mayer M.G., and Lobell M. Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes. Blood 67 (1986) 1721-1730
14. Horiike S., Taniwaki M., Misawa S., and Abe T. Chromosome abnormalities and karyotypic evolution in 83 patients with myelodysplastic syndrome and predictive value for prognosis. Cancer 62 (1988) 1129-1138
15. Mamaev N., Mamaeva S.E., Pavlova V.A., and Patterson D. Combined trisomy 1q and monosomy 17p due to translocation t(1;17) in a patient with myelodysplastic syndrome. Cancer Genet Cytogenet 35 (1988) 21-25
16. Mascarello J.T., Osborn C., and Kadota R.P. A dysmorphic child with myelodysplasia characterized by a duplication of 1q and multiple duplication of 3q. Cancer Genet Cytogenet 38 (1989) 9-12
17. Brandwein J.M., Horsman D.E., Eaves A.C., Eaves C.J., Massing B.G., Wadsworth L.D., et al. Childhood myelodysplasia: suggested classification as myelodysplastic syndromes based on laboratory and clinical findings. Am J Pediatr Hematol Oncol 12 (1990) 63-70
18. Privitera E., Wang W., and Raimondi S.C. Monosomy 7 and unbalanced t(1;7) in an adolescent boy with myelodysplastic syndrome. Leukemia 6 (1992) 742-745
19. Hirose M., Kawahito M., and Kuroda Y. Myelodysplastic syndrome in two young brothers. Br J Haematol 89 (1995) 211-213
20. GFCH. Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the Groupe Francais de Cytogénétique Hématologique. Leukemia 11 (1997) 1478-1485
21. Satake N., Sakashita A., Kobayashi H., Maseki N., Sakurai M., and Kaneko Y. Minimal residual disease in acute monocytic leukemia patient with trisomy 11 and partial tandem duplication of MLL. Cancer Genet Cytogenet 96 (1997) 26-29
22. Forrest D.L., Couban S., Nevill T.J., Lee C.Y.L., and Welch P.J. Myelodysplastic syndrome and a nonrandom chromosomal abnormality t(1;19): an indolent pathologic entity. Cancer Genet Cytogenet 122 (2000) 134-136
23. Kardos G., Baumann I., Passmore S.J., Locatelli F., Hasle H., Schultz K.R., et al. Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7. Blood 102 (2003) 1997-2003
24. Rubin C.M., Arthur D.C., Woods W.G., Lange B.J., Nowell P.C., Rowley J.D., et al. Therapy-related myelodysplastic syndrome and acute myeloid leukaemia in children: correlation between chromosomal abnormalities and prior therapy. Blood 78 (1991) 2982-2988
25. Winick N.J., McKenna R.W., Shuster J.J., Schneider N.R., Borowitz M.J., Bowman W.P., et al. Secondary acute myeloid leukemia in children with acute lymphoblastic leukemia treated with etoposide. J Clin Oncol 11 (1993) 209-217
26. Harrison C.J., Cuneo A., Clark R., Johansson B., Lafage-Pochitaloff M., Mugneret F., et al. Ten novel 11q23 chromosomal partner sites. Leukemia 12 (1998) 811-822
27. Tsurusawa M., Manabe A., Hayashi Y., Akiyama Y., Kigasawa H., Inada H., et al. Therapy-related myelodysplastic syndrome in childhood: a retrospective study in 36 patients in Japan. Leuk Res 29 (2005) 625-632