The Translocation t(8;16)(p11;p13) Defines an AML Subtype with Distinct Cytology and Clinical Features

References

• 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 Cooperative Group. Ann. Intern. Med. 1985; 103: 620–625
   PubMed Web of Science ®Google Scholar
• Second MIC Cooperative Study Group. Morphologic, immunologic, and cytogenetic (MIC) working classification of the acute myeloid leukemias. Cancer Genet. Cytogenet. 1988; 30: 1–15
   PubMed Web of Science ®Google Scholar
• Larson R. A., Kondo K., Vardiman J. W., Butler A. E., Golomb H. M., Rowley J. D. Evidence for a 15;17 translocation in every patient with acute promyelocytic leukemia. Am. J. Med. 1984; 76: 827–841
   PubMed Web of Science ®Google Scholar
• Heim S., Kristoffersson U., Mandahl N., Mitelman F., Bekassy A. N., Garwicz S., Wiebe T. High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia. Cancer Genet. Cytogenet. 1986; 22: 195–201
   PubMed Web of Science ®Google Scholar
• Heim S., Avanzi G. C., Billstrom R., Kristoffersson U., Mandahl N., Bekassy A. N., Garwicz S., Wiebe T., Pegoraro L., Falda M., Resegotti L., Mitelman F. A new specific chromosomal rearrangement t(8;16)(p11;p13) in acute monocytic leukaemia. Br. J. Haematol. 1987; 66: 323–326
   PubMed Web of Science ®Google Scholar
• Bertheas M. F., Jaubert J., Vasselon C., Reynaud J., Pomier G., Le Petit J. C., Hagemeijer A., Brizard C. P. A complex t(3;8;17) involving breakpoint 8p11 in a case of M5 acute nonlymphocytic leukemia with erythrophagocytosis. Cancer Genet. Cytogenet. 1989; 42: 62–73
   Web of Science ®Google Scholar
• Brizard A., Guilhot F., Huret J. L., Benz-Lemoine E., Tanzer J. The 8p11 anomaly in “monoblastic., leukaemia. Leuk. Res. 1988; 12: 693–697
   PubMed Web of Science ®Google Scholar
• Tanzer J., Brizard A., Guilhot F., Benz-Lemoine E., Drefus B., Lessard M., Herchkovitch C., Mossafa H., Davi F., Huret J., Le Bezu M. La leucémie aiguë a translocation (8;16). Nouv. Rev. Fr. Hematoi 1988; 30: 83–87
   PubMedGoogle Scholar
• Yam L. T., Li C. Y., Crosby W. H. Cytogenetic identification of monocytes and granulocytes. Am. J. Clin. Pathol 1971; 55: 283–290
   PubMed Web of Science ®Google Scholar
• Laï J. L., Zandecki Joulet M., Savary J. P.J. B., Lambiliotte A., Bauters F., Cosson A., Deminatti M. Three cases of translocation (8;16)(p11;p13) observed in acute myelomonocytic leukemia: a new specific subgroup. Cancer Genet. Cytogenet. 1987; 27: 101–109
   PubMed Web of Science ®Google Scholar
• Brookwell R., Hunt F. A. Translocation (8;16) in acute myelomonocytic leukemia. Cancer Genet. Cytogenet. 1988; 32: 297–298
   PubMed Web of Science ®Google Scholar
• Barbata G., Carbone P., Mirto S., Santor A., Giglio M. C., Granata G. Translocation t(8;16)(p11;p13) in acute nonlymphoblastic leukemia (M4) possibly secondary to Hodgkin's disease. Cancer Genet. Cytogenet. 1989; 37: 127–131
   PubMed Web of Science ®Google Scholar
• Wessels J. W., Mollevanger P., Dauwerse J. G., Cluitmans F. H. M., Breuning M. H., Beverstock G. C. Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia. Blood 1991; 11: 1555–1559
   Google Scholar
• Zandecki M., Laï J. L., Mazingue F., Lepelley P., Chassaing O., Farriaux J. P., Deminatti M., Cosson A. Congenital acute monoblastic leukemia with double translocation (8;16)(p11;p13) and (16;20)(q13;p13). Nouv. Rev. Fr. Hematoi 1988; 30: 247–250
   PubMed Web of Science ®Google Scholar
• Smadja N., Gramont A., Gonzalez-Canali G., Krulik M., Deloup J. Another case of acute myelomonocytic leukemia with t(8;16)(p11;p13). Cancer Genet. Cytogenet. 1988; 36: 137–139
   PubMed Web of Science ®Google Scholar
• Ritter H. L., Weiden P. L., Jr. Unusual association of bone marrow necrosis, disseminated intravascular coagulation, and a rare 8;16 chromosomal translocation in an adult patient with acute nonlymphatic leukemia. Cancer Genet. Cytogenet. 1987; 24: 243–250
   PubMed Web of Science ®Google Scholar
• Powell B. L., McNay J. W., Brown S., Cooper M. R., Pettenali M. J. Translocation (8;16)(p11;p13) in patients with acute monocytic leukemias. An evolving syndrome. Cancer Genet. Cytogenet. 1988; 36: 109–115
   PubMed Web of Science ®Google Scholar
• Bernstein R., Pinto M. R., Spector I., MacDougall L. G. A unqiue 8;16 translocation in 2 infants with poorly differentiated monoblastic leukemia. Cancer Genet. Cytogenet. 1987; 24: 213–220
   PubMed Web of Science ®Google Scholar
• Becher R., Haas O. A., Graeven U., Bettelheim P., Ambros P., Fridrik M., Schaefer U. W., Schmidt C. G. Translocation t(8;16) in acute monocytic leukemia. Cancer Genet. Cytogenet. 1988; 34: 265–271
   PubMed Web of Science ®Google Scholar
• Fenaux P., Vanhaesbroucke C., Estienne M. H., Preud'homme C., Pagniez D., Facon T., Millot F., Bauters F. Acute monocytic leukaemia in adults: treatment and prognosis in 99 cases. Br. J. Haematol. 1990; 75: 41–48
   PubMed Web of Science ®Google Scholar
• Talarico L., Weintraub L. R. Leukocytic fibrinolysis in myelomonocytic leukemia. Cancer 1977; 39: 1618–1624
   PubMed Web of Science ®Google Scholar
• Van Slyck E. J., Raman S. B. K., Janakiraman N. Primary fibrinolysis in acute monocytic leukemia. Henry Ford Hosp. Med. J. 1989; 37: 33–36
   PubMedGoogle Scholar
• Bloomfield C. D., Arthur D. C., Wurster-Hill D., Testa J., Tantravahi R., Shanske A., Warburton D., Le Beau M., Nelson D., Davey F., Mayer R., Schiffer C., Anderson J. Recurring chromosome abnormalities in de novo AML. A preliminary report of CALGB 8461. Abstract 9th International Workshop on Human Gene Mapping, Paris, 1987; 49
   Google Scholar
• Raimondi S. C., Kalwinsky D. K., Hayashi Y., Behm F. G., Mirro J., Jr, Williams D. L. Cytogenetics of childhood acute nonlymphocytic leukemia. Cancer Genet. Cytogenet. 1989; 40: 13–27
   PubMed Web of Science ®Google Scholar
• Jujena H. S., Elder F. F. B., Rajaraman S. Acute monoblastic leukemia with a single chromosomal rearrangement involving breakpoints on chromosomes 8 and 16, 46, XX, t(8;16)(p11;p13). Acta Haematol 1987; 78: 1–5
   Web of Science ®Google Scholar
• Wilcoxen H., Murcek M., Decatur T., Schleicher S., Thiel K. Acute monocytic leukemia associated with translocation t(8;16)(p11;p13). Karyogram 1988; 14: 77
   Google Scholar
• Schouten T. J., Hustinx T. W., Scheres J. M. J.C., Holland R., Vann G. A. M. Malignant histiocytosis, clinical and cytogenetic studies in a newborn and a child. Cancer 1983; 52: 1229–1236
   PubMed Web of Science ®Google Scholar
• Schmalzl F., Huhn D., Asamer H., Abbrederis K., Braunsteiner H. Atypical (monomyelocytic) myelogenous leukaemia: cytochemical, electron microscopic, and biochemical investigations. Acta Haematol 1972; 48: 72–88
   PubMed Web of Science ®Google Scholar
• Tavassoli M., Shaklai M., Crosby W. H. Cytochemical diagnosis of acute myelomonocytic leukemia. Am. J. Clin. Pathol 1979; 72: 59–62
   PubMed Web of Science ®Google Scholar
• Li C. Y., Phyliky R. L., Yam L. T. Acute myelomonocytic leukemia: an unusual variant with both granulocytic and monocytic esterases in the leukemic cells. Mayo Clin. Proc 1986; 61: 104–109
   PubMed Web of Science ®Google Scholar
• Huhn D., Twardzik L. Acute myelomonocytic leukemia and the French-American-British classification. Acta Haematol. 1983; 69: 36–40
   PubMed Web of Science ®Google Scholar
• Tubbs R. R., Valenzuela R., Savage R. A., Deodhar S. D. The nature of surface immunoglobulin in pure monocytic (M5) leukemia. Am. J. Clin. Pathol. 1979; 72: 614–617
   PubMed Web of Science ®Google Scholar
• Wheeler M. S., Wilson E. C., Stass S. A. Erythroleukophagocytosis by leukemic cells-A nonspecific finding (letter). Am. J. Clin. Pathol 1981; 75: 266–267
   PubMed Web of Science ®Google Scholar
• Rowley J. D., Potter D. Chromosomal banding patterns in acute nonlymphocytic leukemia. Blood 1976; 47: 705–721
   PubMed Web of Science ®Google Scholar
• Larson R. A., Le Beau M. M., Vardiman J. W., Testa J. R., Golomb H. M., Rowley J. D. The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: A 12 year study (1970-1982). Cancer Genet. Cytogenet. 1983; 10: 219–236
   PubMed Web of Science ®Google Scholar
• Berger R., Bernheim A., Le Coniat M., Vecchione D., Pacot A., Daniel M.-T., Flandrin G. Abnormalities of the short arm of chromosome 12 in acute nonlymphocytic leukemia and dysmyelopoietic syndrome. Cancer Genet. Cytogenet. 1986; 19: 281–289
   PubMed Web of Science ®Google Scholar
• Palka G., Fioritoni G., Geraci L., Calabrese G., Mosca L., Peca S., Guanciali-Franchi P., Spadano A., Arduini A., Torlontano G. Cytogenetics and acute non lymphocytic leukemia. Ann. Genet. 1987; 30: 39–46
   PubMedGoogle Scholar
• Larson R. A., Werali M., Le Beau M. M., Daly K. M., Pape L. H., Rowley J. D., Vardiman J. W. Short remission durations in therapy-related leukemia despite cytogenetic complete responses to high-dose cytarabine. Blood 1988; 72: 1333–1339
   PubMed Web of Science ®Google Scholar
• Shikano T., Ishikawa Y., Ohkawa M., Hatayama Nakadate Y. H., Hatae Y., Takeda T. Karyotypic changes from initial diagnosis to relapse in childhood acute leukemia. Leukemia 1990; 4: 419–422
   PubMed Web of Science ®Google Scholar
• Odom L. F., Gordon E. M. Acute monoblastic leukemia in infancy and early childhood: successful treatment with an epipodophyllotoxin. Blood 1984; 64: 875–882
   PubMed Web of Science ®Google Scholar
• Dauwerse J. G., Kievits K., Beverstock G. C., Van der Keur D., Smit E., Wessels J. W., Hagemeijer A., Pearson P. L., Van Ommen G. J. B., Breuning M. H. Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4, regional localisation of the breakpoint in 16p. Cytogenet Cell Genet. 1990; 3: 126–128
   Google Scholar
• Heim S., Mitelman F. Proliferation-specific and differentiation associated chromosomal breakpoints in human neoplasia, a unifying model. Hereditas 1986; 104: 307–312
   PubMed Web of Science ®Google Scholar
• Wilson E. L., Jacobs P., Dowdle E. B. The secretion of plasminogen activators by human myeloid leukemic cells in vitro. Blood 1983; 61: 568–574
   PubMed Web of Science ®Google Scholar
• Jacobs P., Martell R. W., Wilson E. L. Chemotherapy of adult acute nonlymphoblastic leukaemia. Haematologia-Budap. 1990; 23: 27–40
   PubMedGoogle Scholar
• Hamaguchi M., Morishita Y., Takahashi I., Ogura M., Takamatsu J., Saito H. FDP D- dimer induces the secretion of interleukin-1, urokinase-type plasminogen activator, and plasminogen activator inhibitor-2 in a human promonocytic leukemia cell line. Blood 1991; 11: 94–100
   Google Scholar