115
Views
51
CrossRef citations to date
0
Altmetric
Original Article

Disease Features in Acute Myeloid Leukemia with t(8;21)(q22;q22). Influence of Age, Secondary Karyotype Abnormalities, CD19 Status, and Extramedullar Leukemia on Survival

, , , , , , , , , & show all
Pages 67-77 | Received 25 Apr 2000, Published online: 01 Jul 2009

References

  • Rowley J. D. A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and Giemsa staining. Nature 1973; 243: 290–293
  • Bennett J. M., Catovsky D., Daniel M. T., Flandrin G., Galton D.A.G., Gralnick H. R., Sultan C. Proposals for the classification of the acute leukaemias. French-American-British (FAB) Co-operative Group. British Journal of Haematology 1976; 33: 451–458
  • Bennett J. M., Catovsky D., Daniel M. T., Flandrin G., Galton D.A.G., Gralnick H. R., Sultan C. Proposed revised criteria for the classification of acute myeloid leukaemia. A report of the French-American-British Co-operative Group. Annals of Internal Medicine 1985; 103: 620–625
  • Swirsky D. M., Li Y. S., Matthews J. G., Flemans R. J., Rees K. H., Hayhoe F.G.J. 8;21 translocation in acute granulocytic leukaemia: cytological, cytochemical and clinical features. British Journal of Haematology 1984; 56: 199–213
  • Hurwitz C. A., Raimondi S. C., Head D., Krance R., Mirro J., Kalwinsky D. K., Ayers G. D., Behm F. G. Distinctive immunophenotypic features of t(8;21)(q22;q22) acute myeloblastic leukemia in children. Blood 1992; 80: 3182–3187
  • Yamasaki H., Era T., Asou N., Sanada I., Matutes E., Yamaguchi K., Takatsuki K. High degree of myeloid differentiation and granulocytosis is associated with t(8;21) smoldering leukemia. Leukemia 1995; 9: 1147–1153
  • Erickson P., Gao J., Chang K-S., Look T., Whisenant E., Raimondi S., Lasher R., Trujillo J., Rowley J., Drabkin H. Identification of breakpoints in t(8;21) acute myelogenous leukemia and isolation of a fusion transcript, AML1/ETO with similarity to Drosophila Segmentation Gene, runt. Blood 1992; 80: 1825–1831
  • Fenaux P., Preudhomme C., Lai J. L., Morel P., Beuscart R., Bauters F. Cytogenetics and their prognostic value in de novo acute myeloid leukaemia: a report on 283 cases. British Journal of Haematology 1989; 73: 61–67
  • Grimwade D., Walker H., Oliver F., Wheatley K., Harrison C., Harrison G., Rees J., Hann I., Stevens R., Burnett A., Goldstone A. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. Blood 1998; 92: 2322–2333
  • Byrd J. C., Weiss R. B., Arthur D. C., Lawrence D., Baer M. R., Davey F., Trikha E. S., Carroll A. J., Tantravahi R., Qumsiyeh M., Patil S. R., Moore J. O., Mayer R. J., Schiffer C. A., Bloomfield C. D. Extramedullar leukemia adversely affects hematological complete remission rate and overall survival in patients with t(8;21)(q22;q22) results from Cancer and Leukemia Group B 8461. Journal of Clinical Oncology 1997; 15: 466–475
  • Bennett J. M., Catovsky D., Daniel M. T., Flandrin G., Galton D.A.G., Gralnick H. R., Sultan C. The French-American-British Co-operative Group. Proposals for the classification of the myelodysplastic syndromes. British Journal of Haematology 1982; 51: 189–199
  • ISCN. An international system for human cytogenetic nomenclature, F. Mitelman;. S Karger, Basel 1995; 1995
  • Peto R., Pike M. C., Armitage P., Breslow N. E., Cox D. R., Howard S. V., Mantel N., McPherson K., Peto J., Smith P. G. Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II Analysis and examples. British Journal of Cancer 1977; 35: 1–39
  • O'Brien S., Kantarjian H. M., Keating M., Gagnon G., Cork A., Trujillo J., McCredie K. B. Association of granulocytosis with poor prognosis in patients with acute myelogenous leukemia and translocation of chromosomes 8 and 21. Journal of Clinical Oncology 1989; 7: 1081–1086
  • Groupe Francais de Cytogenetique Hematologique. Acute myelogenous leukemia with an 8;21 translocation, A Report on 148 Cases from the Groupe Francais de Cytogenetique Hematologique. Cancer Genetics and Cytogenetics 1990; 44: 169–179
  • Rege K. P., Janes S. L., Saso R., Min T., Swansbury J., Powles R. L., Treleaven J. G. Secondary leukaemia characterized by monosomy 7 occurring post-autologous stem cell transplantation for AML. Bone Marrow Transplantation 1998; 21: 853–855
  • Second International Workshop on Chromosomes in Leukemia. Cytogenetic, morphologic and clinical correlations in acute nonlymphocytic leukemia with t(8q-;21q+). Cancer Genetics and Cytogenetics 1979; 2: 99–102
  • Schoch C., Haase D., Haferlach T., Gudat H., Freund M., Link H., Lengfelder E., Wandt H., Sauerland M. C., Loffler H., Fonatsch C. Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22) an additional deletion of 9q is an adverse prognostic factor. Leukemia 1996; 10: 1288–1295
  • Langabeer S. E., Walker H., Rogers J. R., Burnett A. K., Wheatley K., Swirsky D., Goldstone A. H., Linch D. L. Incidence of AML1/ETO fusion transcripts in patients entered into the MRC AML trials. British Journal of Haematology 1997; 99: 925–928
  • Byrd J. C., Edenfield W. J., Shields D. J., Dawson N. A. Extramedullary myeloid cell tumors in acute nonlymphocytic leukemia: a clinical review. Journal of Clinical Oncology 1995; 13: 1800–1816
  • Carbonell F., Swansbury J., Min T., Matutes E., Buccheri V., Morilla R., Seeker-Walker L., Catovsky D. Cytogenetic findings in acute biphenotypic leukemia. leukemia 1996; 10: 1283–1287
  • Luckit J., Bain B., Matutes E., Min T., Pinkerton R., Catovsky D. Teaching cases from the Royal Marsden and St Mary's hospitals. Case 1998; 13, An orbital mass in a young girl. Leukemia & Lymphoma; 28:621-622
  • Hiorns L. R., Swansbury G. J., Zomas A., Catovsky D. Letter: Partial trisomy of chromosome 4 resulting from a novel t(4;7) translocation in a case of AML M2 with eosinophilia. Cancer Genetics and Cytogenetics 1996; 86: 89–91
  • Calabrese G., Palka G., Min T., Stuppia L., Swansbury J. G., Powles R., Morizio E., Peila R., Donti E., Fioritoni G. Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by FISH analysis. Cancer Genetics and Cytogenetics 1996; 91: 40–45

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.