Fluorescence in situ hybridization in combination with morphology detects minimal residual disease in remission and heralds relapse in acute leukaemia

British Journal of Haematology

Volumn 95, Issue 4, 1996, Pages 666-672

  Bernell, Per ^a   Arvidsson, Ingrid ^a   Jacobsson, Björn ^a   Hast, Robert ^a  

^a DANDERYD HOSPITAL   (Sweden)

Author keywords

acute leukaemia; cytogenetics; fluorescence in situ hybridization; minimal residual disease; morphology

Indexed keywords

ACUTE LEUKEMIA; ADULT; AGED; ARTICLE; CANCER RECURRENCE; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; MALE; MINIMAL RESIDUAL DISEASE; MORPHOLOGY; PRIORITY JOURNAL;

EID: 0030458650     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1996.d01-1945.x     Document Type: Article

References (18)

1. Anastasi, J., Vardiman, J.W., Rudinsky, R., Patel, M., Nachman, J., Rubin, C.M. & Le Beau, M.M. (1991) Direct correlation of cytogenetic findings with cell morphology using in situ hybridization and analysis of suspicious cells in bone marrow specimens of two patients completing therapy for acute lymphoblastic leukemia. Blood, 77, 2456-2462.
2. Bennett, J.M., Catovsky, D., Daniel, M.T., Flandrin, G., Galton, D.A.G., Gralnick, H.R. & Sultan, C., The French-American-British (FAB) Co-operative Group (1976) Proposals for the classification of the acute leukaemias. British Journal of Hematology, 33, 451-458.
3. Bernell, P., Jacobsson, B., Nordgren, A. & Hast, R. (1996) Clonal cell lineage involvement in myelodysplastic syndromes studied by fluorescence in situ hybridization and morphology. Leukemia, 10, 662-668.
4. Bernell, P., Kimby, E. & Hast, R. (1994) Recombinant human granulocyte-macrophage colony-stimulating factor in combination with chemotherapy in acute myeloid leukemia after myelodysplastic syndromes. Leukemia, 8, 1631-1639.
5. Campana, D. & Pui, C-H. (1995) Detection of minimal residual disease in acute leukemia: Methodologic advances and clinical significance. Blood, 85, 1416-1434.
6. Cavé, H., Guidal, P., Rohrlich, P., Delfau, M.H., Broyart, A., Lescoeur, B., Rahimy, C., Fenneteau, O., Monplaisir, N., D'Auriol, L., Elion, J., Vilmer, E. & Grandchamp, B. (1994) Prospective monitoring and quantitation of residual blasts in childhood acute lymphoblastic leukemia by polymerase chain reaction study of delta and gamma T-cell receptor genes. Blood, 85, 1892-1902.
7. Cremer, T., Landegent, J., Bruchner, A., Scholl, H.P., Schardin, M., Hager, H.D., Devillee, P., Pearsson, P. & van den Ploeg, M. (1986) Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe LL84. Human Genetics, 74, 346-352.
8. Engel, H., Goddacre, A., Keyhani, A., Jiang, S., Van, N.T., Kimmel, M., Sanchez-Williams, G. & Andreeff, M. (1995) Detection of minimal residual disease in acute myelogenous leukemia and myelodysplastic syndromes in clinical remission by molecular cytogenetics. Blood, 86, (Suppl. 1), 1059a.
9. Freireich, E.J., Cork, A., Stass, S.A., McCredie, K.B., Keating, M.J., Estey, E.H., Kantarijan, H.M. & Trujillo, J.M. (1992) Cytogenetics for detection of minimal residual disease in acute myeloblastic leukemia. Leukemia, 6, 500-506.
10. ISCN (1991) Guidelines for Cancer Cytogenetics: Supplement to An International System for Human Cytogenetic Nomenclature (ed. by F. Mitelman). S. Karger, Basel.
11. Jacobsson, B., Bernell, P., Arvidsson, I. & Hast, R. (1996) Combination of classical morphology and interphase cytogenetics on routine peripheral blood and bone marrow smears. Journal of Histochemistry and Cytochemistry, in press.
12. Jenkins, R.B., Le Beau, M.M., Kraker, W.J., Borell, T.J., Stalboerger, P.G., Davis, E.M., Penland, L., Fernald, A., Espinosa, R., III, Schaid, D.J., Noel, P. & Dewald, G.W. (1992) Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens. Blood, 79, 3307-3315.
13. Lo Coco, F., Diverio, D., Pandolfi, P.P., Biondi, A., Rossi, V., Avvisati, G., Rambaldi, A., Arcese, W., Petti, M.C., Meloni, G., Mandelli, F., Grignani, F., Masera, G., Barbui, T. & Pelicci, P.G. (1993) Molecular evaluation of residual disease as a predictor of relaps in acute promyelocytic leukaemia. Lancet, 340, 1437-1438.
14. Nylund, S., Ruutu, T., Saarinen, U. & Knuutila, S. (1994a) Metaphase fluorescence in situ hybridiazation (FISH) in the follow-up of 60 patients with haemopoietic malignancies. British Journal of Haematology, 88, 778-783.
15. Nylund, S.J., Ruutu, T., Saarinen, U., Larramendy, M.L. & Knuutila, S. (1994b) Detection of minimal residual disease during fluorescence DNA in situ hybridization: a follow-up study in leukemia and lymphoma patients. Leukemia, 8, 587-594.
16. Pinkel, D., Siraume, T. & Gray, J.W. (1986) Cytogenetic analysis using quantative, high-sensitivity, fluorescence hybridization. Proceedings of the National Academy of Sciences of the United States of America, 83, 2934-2958.
17. Van Lom, K., Hagemeijer, A., Smit, E.M.E. & Löwenberg, B. (1993) In situ hybridization on May-Grünwald-Giemsa-stained bone marrow and blood smears of patients with hematologic disorders allow detection of cell-lineage-specific cytogenetic abnormalities. Blood, 82, 884-888.
18. White, D.M., Crolla, J.A. & Ross, F.M. (1995) Detection of minimal residual disease in childhood acute lymphoblastic leukaemia using fluorescence in situ hybridization. British Journal of Haematology, 91, 1019-1024.