Chromosomal Aberrations in Progressive and Indolent Chronic B-Lymphocytic Leukaemia: A longitudinal study

Authors

  • G. Juliusson Division of Clinical Haematology and Oncology, Department of Medicine, The Department of Clinical Immunology, Huddinge Hospital, The Department of Medical Cell Genetics, Medical Nobel Institute, Karolinska Institute, Stockholm, Sweden
  • K. Friberg Division of Clinical Haematology and Oncology, Department of Medicine, The Department of Clinical Immunology, Huddinge Hospital, The Department of Medical Cell Genetics, Medical Nobel Institute, Karolinska Institute, Stockholm, Sweden
  • G. Gahrton Division of Clinical Haematology and Oncology, Department of Medicine, The Department of Clinical Immunology, Huddinge Hospital, The Department of Medical Cell Genetics, Medical Nobel Institute, Karolinska Institute, Stockholm, Sweden

DOI:

https://doi.org/10.3109/02841868809093573

Keywords:

Leukaemia, B-CLL, chromosomes, longitudinal study

Abstract

Chromosome analyses of B-cell mitogen-activated cells from 95 patients with chronic B-lymphocytic leukaemia revealed clonal chromosomal aberrations in 50 patients (53%), of which 24 had an extra chromosome 12 with or without other aberrations. Patients with clonal aberrations, especially those with +12, had poorer survival than other patients. Longitudinal studies, with a mean of 3.5 samplings during a median interval of 3.5 years, were performed in 41 patients, of which 24 (59%) had progressive disease. Twenty-nine of the patients in the longitudinal study (71%), 16 with and 13 without clonal aberrations, reatained their karyotype unaltered. In 6 patients a clonal aberration was found only once. Six patients showed minor changes of the karyotype. The karyotype seems to be established at diagnosis, and marks the disease of the individual CLL-patient.

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Published

1988-01-01

How to Cite

Juliusson, G., Friberg, K., & Gahrton, G. (1988). Chromosomal Aberrations in Progressive and Indolent Chronic B-Lymphocytic Leukaemia: A longitudinal study. Acta Oncologica, 27(5), 473–477. https://doi.org/10.3109/02841868809093573