BACKGROUND AND METHODS. Specific chromosomal abnormalities have been shown to affect the overall survival of patients with acute leukemia, but the possibility that specific chromosomal defects may influence the course of B-cell chronic lymphocytic leukemia (CLL) is controversial. We assessed this possibility as follows: blood mononuclear cells from 433 patients with B-cell CLL in five European centers were cultured with B-cell mitogens, and banded metaphases were studied. RESULTS. Three hundred ninety-one patients could be evaluated cytogenetically, and 218 had clonal chromosomal changes. The most common abnormalities were trisomy 12 (n = 67) and structural abnormalities of chromosome 13 (n = 51; most involving the site of the retinoblastoma gene) and of chromosome 14 (n = 41). Patients with a normal karyotype had a median overall survival of more than 15 years, in contrast to 7.7 years for patients with clonal changes. Patients with single abnormalities (n = 113) did better than those with complex karyotypes (P less than 0.001). Patients with abnormalities involving chromosome 14q had poorer survival than those with aberrations of chromosome 13q (P less than 0.05). Among patients with single abnormalities, those with trisomy 12 alone had poorer survival than patients with single aberrations of chromosome 13q (P = 0.01); the latter had the same survival as those with a normal karyotype. A high percentage of cells in metaphase with chromosomal abnormalities, indicating highly proliferative leukemic cells, was associated with poor survival (P less than 0.001). Cox proportional-hazards analysis identified age, sex, the percentage of cells in metaphase with chromosomal abnormalities, and the clinical stage of the disease (Binet classification system) as independent prognostic variables. CONCLUSIONS. Chromosomal analysis provides prognostic information about overall survival in addition to that supplied by clinical data in patients with B-cell CLL.
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Department of Medicine, Karolinska Institute, Huddinge Hospital, Sweden.
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[Abstract][Full Text]
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[Abstract][Full Text]
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[Abstract][Full Text]
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[Abstract][Full Text]
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[Abstract][Full Text]
Kalil, N., Cheson, B. D.
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[Abstract][Full Text]
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(1999). Ig V Gene Mutation Status and CD38 Expression As Novel Prognostic Indicators in Chronic Lymphocytic Leukemia. Blood
94: 1840-1847
[Abstract][Full Text]
Hamblin, T. J., Davis, Z., Gardiner, A., Oscier, D. G., Stevenson, F. K.
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94: 1848-1854
[Abstract][Full Text]
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93: 4365-4374
[Abstract][Full Text]
Cuneo, A., Bigoni, R., Rigolin, G. M., Roberti, M. G., Bardi, A., Piva, N., Milani, R., Bullrich, F., Veronese, M. L., Croce, C., Birg, F., Dohner, H., Hagemeijer, A., Castoldi, G.
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93: 1372-1380
[Abstract][Full Text]
Caligaris-Cappio, F., Hamblin, T. J.
(1999). B-Cell Chronic Lymphocytic Leukemia: A Bird of a Different Feather. JCO
17: 399-399
[Abstract][Full Text]
Malik, Z., Rothmann, C., Cycowitz, T., Cycowitz, Z. J., Cohen, A. M.
(1998). Spectral Morphometric Characterization of B-CLL Cells Versus Normal Small Lymphocytes. J. Histochem. Cytochem.
46: 1113-1118
[Abstract][Full Text]
Corcoran, M. M., Rasool, O., Liu, Y., Iyengar, A., Grander, D., Ibbotson, R. E., Merup, M., Wu, X., Brodyansky, V., Gardiner, A. C., Juliusson, G., Chapman, R. M., Ivanova, G., Tiller, M., Gahrton, G., Yankovsky, N., Zabarovsky, E., Oscier, D. G., Einhorn, S.
(1998). Detailed Molecular Delineation of 13q14.3 Loss in B-Cell Chronic Lymphocytic Leukemia. Blood
91: 1382-1390
[Abstract][Full Text]
Thompson, A. A., Talley, J. A., Do, H. N., Kagan, H. L., Kunkel, L., Berenson, J., Cooper, M. D., Saxon, A., Wall, R.
(1997). Aberrations of the B-Cell Receptor B29 (CD79b) Gene in Chronic Lymphocytic Leukemia. Blood
90: 1387-1394
[Abstract][Full Text]
Gahn, B., Schafer, C., Neef, J., Troff, C., Feuring-Buske, M., Hiddemann, W., Wormann, B.
(1997). Detection of Trisomy 12 and Rb-Deletion in CD34+ Cells of Patients With B-Cell Chronic Lymphocytic Leukemia. Blood
89: 4275-4281
[Abstract][Full Text]
Dohner, H., Stilgenbauer, S., James, M. R., Benner, A., Weilguni, T., Bentz, M., Fischer, K., Hunstein, W., Lichter, P.
(1997). 11q Deletions Identify a New Subset of B-Cell Chronic Lymphocytic Leukemia Characterized by Extensive Nodal Involvement and Inferior Prognosis. Blood
89: 2516-2522
[Abstract][Full Text]
Panayiotidis, P., Ganeshaguru, K., Hoffbrand, A.V., Rowntree, C., Jabbar, S.A.B., Foroni, L.
(1997). Deletion of 13q14.3 and Not 13q12 Is the Most Common Genetic Abnormality Detected in Chronic Lymphocytic Leukemia Cells. Blood
89: 734-735
[Full Text]
Gallego, M. I., Lazo, P. A.
(1995). Deletion in Human Chromosome Region 12q13-15 by Integration of Human Papillomavirus DNA in a Cervical Carcinoma Cell Line. J. Biol. Chem.
270: 24321-24326
[Abstract][Full Text]
(1990). CHROMOSOMAL ABNORMALITIES HAVE PROGNOSTIC VALUE IN CLL. JWatch General
1990: 6-6
[Full Text]