Acute Lymphoblastic Leukaemia in Infancy: Clinical and Biological Features

References

• Reaman Zeltzer G., Bleyer P., Amedola W. A., Level B., Sather C.H., Hammond D. Acute lymphoblastic leukemia in infants less than one year of age: A cumulative experience of the Children's Cancer Study Group. J. Clin. Oncol. 1985; 3: 1513–1521
   PubMed Web of Science ®Google Scholar
• Crist Pullen W., Boyett J., Falleta J., VanEys J., Borowitz J., Jackson M., Dowell J., Frankel B., Quddus L., Ragab F.A., Vietta T. Clinical and biological features predict a poor prognosis in acute lymphoid leukemias in infants; A Pediatric Oncology Study. Blood 1986; 67: 135–140
   PubMed Web of Science ®Google Scholar
• Leiper A, Chessells J. M. Acute lymphoblastic leukaemia under two years. Arch. Dis. Child. 1986; 61: 1007–1012
   PubMed Web of Science ®Google Scholar
• Pui C, Williams H., Raimondi D., Melvin S. C., Behm S. L., Look F. G., Dahl A. T., Rivera G. V., Kalwinsky G. K., Mirro D. K., Dodge J.D.K., Murphy S. B. Unfavorable presenting clinical and laboratory features are associated with CALLA-negative non-B, non-T lymphoblastic leukemia in children. Leukaemia Research 1986; 10: 1287–1292
   PubMed Web of Science ®Google Scholar
• Katz Malcolm F. E., Gibbons S., Tilley B., Lam R., Robertson G., Czepulkowski M. E.B., Chessells J. M. Cellular and molecular studies on infant null acute lymphoblastic leukemia. Blood 1988; 71: 1438–1447
   PubMed Web of Science ®Google Scholar
• Kaneko Shikano Y., Meseki T., Sakurai N., Takeda M., Hujoshi T., Mimaya Y.J., Fujimoto T. Clinical characteristics of infant acute leukemia with or without 11q23 translocations. Leukemia 1988; 2: 672–676
   PubMed Web of Science ®Google Scholar
• Ludwig W, Bartram D., Harbott C. R., Koller J., Haas U., Hansen-Hagge O. A., Heil T., Seibt-Jung G., Teichman H., Ritter J. V., Knapp J., Gadner W., Theil H.E., Riehm H. Phenotypic and genotypic heterogeneity in infant acute leukemia. 1. Acute lymphoblastic leukemia. Leukemia 1989; 3: 431–439
   PubMed Web of Science ®Google Scholar
• Dinndorf P. A., Reaman G. H. Acute lymphoblastic leukaemia in infants: evidence for B cell origin of disease by monoclonal antibody phenotyping. Blood 1986; 67: 975–978
   Google Scholar
• Pui C, Raimondi H., Murphy S. C., Ribero S. B., Kalwinsky R. C., Dahl D. C., Crist G. V.W.M., Williams D. L. An analysis of leukemic chromosomal features in infants. Blood 1987; 69: 1289–1293
   PubMed Web of Science ®Google Scholar
• Raimondi Peiper S. C., Kitchingman S. C., Behm G. R., Williams F. G., Hancock D. L.M.L., Mirro J. Childhood acute lymphoblastic leukemia with chromosomal breakpoints at 11q23. Blood 1989; 73: 1627–1634
   PubMed Web of Science ®Google Scholar
• Nagasaka Maeda S., Chen H.H, Kita L., Mabunchi K., Misu O., Matsuo H.T., Sugiyama T. Four cases of t(4;11) acute leukemia and its myelomonocytic nature in infants. Blood 1983; 61: 1174–1181
   PubMed Web of Science ®Google Scholar
• Nadler Korsmeyer L. M., Anderson S. J., Boyd K. C., Slaugenhoupt A. W., Part B., Jensen E., Coaral J., Mayer F., Sallan R. J., Ritz S. E.J., Schlossman S. B cell origin of non-T cell acute lymphoblastic leukemia. A model for discrete stages of neoplastic and normal pre-B cell differentiation. J. Clin. Invest. 1984; 74: 332–340
   PubMed Web of Science ®Google Scholar
• Felix Reaman C. A., Korsmeyer G. H., Hollis S. J., Dinndorf G. F., Wright P. A.J.J., Kirsch I. R. Immunoglobulin and T cell receptor gene configuration in acute lymphoblastic leukemia of infancy. Blood 1987; 70: 536–541
   PubMed Web of Science ®Google Scholar
• Felix Wright C. A., Poplack J. J., Reaman D. G., Cole G. H., Goldman D.P., Korsmeyer S. J. T cell receptor α, γ and β genes in T cell and pre-B cell acute lymphoblastic leukemia. J. Clin. Invest. 1987; 80: 545–556
   PubMed Web of Science ®Google Scholar
• Goorha Bunin R., Mirro N., Murphy J., Cross S. B., Behm A. H., Quertermous F. G., Seidman T.J., Kitchingman G. R. Provocative pattern of rearrangements of the genes for the γ and β chains of the T-cell receptor in human leukemias. Proc. Nat. Acad. Sci. USA 1987; 84: 4547–4551
   PubMed Web of Science ®Google Scholar
• Morris Whitham C. M.S.E., Fitzgerald P. H. Transposition of the oncogene c-ets 1 in a t(11;19) (q23, p13) cell line transient during clonal evolution of blast crisis chronic myeloid leukemia. Leukemia 1988; 2: 74–78
   PubMed Web of Science ®Google Scholar
• Bollum F. J. Terminal deocynucleotidyl transferase as a hemopoietic cell marker. Blood 1979; 54: 1203–1215
   PubMed Web of Science ®Google Scholar
• Webber L. M., Garson O. M. Fluorodeoxyuridine synchronization of bone marrow cultures. Cancer Genet. Cytogenet. 1983; 8: 130–132
   Web of Science ®Google Scholar
• Old J. M. Fetal DNA analysis. in “Human Genetic Diseases”, K. E. Davies. IRL., Oxford 1986; 1–17
   Google Scholar
• Mirro Kitchingman J., Williams G., Lauzon D., Lin J., Callahan C.T., Zipf T. Clinical and laboratory characteristics of acute leukemia with the t(4;11) translocation. Blood 1985; 67: 689–697
   Web of Science ®Google Scholar
• Sobol Mick R. E., Royston R., Davey I., Ellison F. R., Newman R. R., Cuttner R., Griffin J., Collins J. D., Nelson H.D.A., Bloomfield C. D. Clinical importance of myeloid antigen expression in adult acute lymphoblastic leukemia. NEJM 1987; 316: 1111–1117
   PubMed Web of Science ®Google Scholar
• Hanesh Kuick S. M., Strahler R., Richardson J., Reaman B., Stoolman G., Hanson L., Nichols C.D., Tueche H. J. Identification of a cellular polypeptide that distinguishes between acute lymphoblastic leukemia in infants and older children. Blood 1989; 73: 527–532
   PubMed Web of Science ®Google Scholar
• Penaux Laf P.J.F., Beuters F. Cytogenetics and their prognostic value in de novo acute non-lymphocytic leukemia (ANLL). Brit. J. Haematol. 1989; 71(suppl. 1)21
   Google Scholar
• Heerena Arthur N. A., Reaman D. C., Sather G. H., Albo H., Feusner V., Lange J., Steinherz B., Zeltzer P.P., Hammond D. Cytogenetics in infants with acute lymphoblastic leukemia (ALL): impact of the 11q23 breakpoint on outcome. Blood 1987; 70(supp. 1)658
   Google Scholar
• Secker-WalkerStewart L., Chan E. L.L, O'Callaghan U., Chessell J. M. The (4;11) translocation in acute leukaemia of childhood: the importance of additional chromosomal aberrations. Brit. J. Haematol. 1985; 61: 101–111
   PubMed Web of Science ®Google Scholar
• Rechavi Simoni-Brok G., Katzir F., Mandel N., Umiel M., Stark T., Zaizov B., Ben-Bassat R.I., Ramot B. More than two immunoglobulin heavy chain J region genes in the majority of infant leukemia. Leukemia 1988; 2: 347–350
   PubMed Web of Science ®Google Scholar
• Kitchingman Mirro G. R., Stass J., Rovigatti S., Melvin U., Williams S. L., Raimondi D. L.S.C., Murphy S. B. Biologic and prognostic significance of the presence of more than two μ heavy chain genes in childhood acute lymphoblastic leukemia of B precursor cell origin. Blood 1986; 67: 698–703
   PubMed Web of Science ®Google Scholar
• Wright Poplack J. J., Bakhshi D. G., Reaman A., Cole G., Jensen D.I.D., Korsmeyer S. J. Gene rearrangements as markers of clonal variation and minimal residual disease in acute lymphoblastic leukemia. J. Clin. Oncol. 1987; 5: 735–741
   PubMed Web of Science ®Google Scholar
• Katz Ball F. E., Gibbons L.B., Chesselk J. M. The use of DNA probes to monitor minimal residual disease in childhood acute lymphoblastic leukaemia. Brit. J. Haematol. 1989; 73: 173–180
   PubMed Web of Science ®Google Scholar
• Alt Yanacopoulos F. W., Blackwell G. D., Wood T. K., Thomas C., Boss E., Coffman M., Rosenberg R., Tonegawa N.S., Baltimore D. Ordered rearrangement of immunoglobulin heavy chain variable region segments. EMBO J. 1984; 3: 1209–1219
   PubMed Web of Science ®Google Scholar
• Bird Galili J., Link J., Stiles M.D, Sklar J. Continuing rearrangement but absence of somatic hyper-mutation in immunoglobulin genes of human B cell precursor leukemia. J. Exp. Med. 1988; 168: 229–245
   PubMed Web of Science ®Google Scholar
• Kinnon C., Katz F. E. Immunoglobulin and T cell receptor gene rearrangement and expression in B-cell acute lymphoblastic leukemia. Leukemia 1989; 3: 808–812
   PubMed Web of Science ®Google Scholar
• Serematix Pellici S., Tabilio P. G., Ubriaco A., Grignani A., Cuttner F., Winchester J., Knowles R.D.M., Dalla Favera R. High frequency of clonal immunoglobulin or T cell receptor gene rearrangements in acute myelogenous leukemias expressing terminal deoxynucleotidyl transferase. J. Exp. Med. 1987; 165: 1703–1712
   PubMed Web of Science ®Google Scholar
• Norton Campana J., Hoffbrand D., Janossy A. V., Coustan-Smith J., Jani E., Yaxley J.J.C., Prentice H. G. Rearrangement of immunoglobulin and T cell antigen receptor genes in acute myeloid leukaemia with lymphoid-associated markers. Leukemia 1987; 1: 757–761
   PubMed Web of Science ®Google Scholar
• Mitzutani Ford S., Wiedemann A. M., Chan L. M., Furley L. C., Greaves A. J. W.M.F., Molgaard H. V. Rearrangement of immunoglobulin heavy chain genes in human T leukaemic cells shows preferential utilization of the D segment (DQ52) nearest to the J region. EMBO J. 1986; 5: 3467–3473
   PubMed Web of Science ®Google Scholar
• Bell G. Human Gene Mapping 9. Ninth International Workshop on Human Gene Mapping. Cytogenet. Cell Genet. 1987; 46: 488–489
   Google Scholar
• de Taisne Gegonne C., Stehelin A., Bernheim D.A., Berger R. Chromosomal location of the human proto-oncogene c-ets. Nature 1984; 310: 581–583
   PubMed Web of Science ®Google Scholar
• Saachi Watson N., Guerts VanKed D. K., Hagemeijer A. H. M., Kersey A., Drabkin J., Patterson H. D.D., Papas T. S. Hu-ets 1 and Hu-ets 2 genes are transposed in acute leukemias with (4;11) and (8;21) translocations. Science 1986; 231: 379–382
   PubMed Web of Science ®Google Scholar
• Human Gene Mapping. Tenth International Workshop on Human Gene Mapping. Cytoget. Cell Genet, (in press) 10. Chromosome 11.
   Google Scholar
• De Braekeleer M., Lin C-C. 4;11 translocation-associated leukemia: a comprehensive analysis. Cancer Genet. Cytogenet. 1985; 21: 53–66
   Web of Science ®Google Scholar
• Sandberg A. A. The chromosomes in acute leukemia. Sem. Haematol. 1986; 23: 201–217
   PubMed Web of Science ®Google Scholar
• Grey Balch E. S., Kohler N. J., Thompson H.W.D., Simpson J. G. Congenital leukaemia: an unusual cause of stillbirth. Arch. Dis. Child 1986; 61: 1001–1006
   PubMed Web of Science ®Google Scholar
• Abe R., Sandberg A. A. Significance of abnormalities involving chromosomal segment 11q23–25 in acute leukemia. Cancer. Genet. Cytogenet. 1984; 13: 121–127
   PubMed Web of Science ®Google Scholar
• Sutherland Jacky G. R., Baker P. B.E., Marvel A. Heritable fragile sites on human chromosomes. ×. New folate sensitive fragile sites 6p23, 9p21 and 11q23. Am. J. Hum. Genet. 1983; 35: 432–437
   PubMed Web of Science ®Google Scholar
• Vim.den Berghe.Malcome J., Katz S., Gibbons F. E., Czepulkowski B., Chlessells B.J.M. Three infants having null acute lymphoblastic leukemia with chromosome rearrangements at 11q23: no involvement of a heritable fragile site in this band. Cytogenet. Cell Genet. 1989; 50: 61–64
   PubMedGoogle Scholar
• Ribero Douglass R., Williams E. C., Raimondi D. L.S.C., Valentine M. Lack of correlation between folate-sensitive and caffeine induced fragile sites and chromosome breakpoints in malignant cells in children. Blood 1986; 68(suppl)263
   PubMedGoogle Scholar
• Greaves M. F. Speculations on the cause of childhood acute lymphoblastic leukemia. Leukemia 1988; 2: 120–125
   PubMed Web of Science ®Google Scholar