TY - JOUR
T1 - Cytogenetic studies in human T-cell lymphoma virus (HTLV)-positive leukemia-lymphoma in the United States
AU - Whang-Peng, J.
AU - Bunn, P. A.
AU - Knutsen, T.
AU - Kao-Shan, C. S.
AU - Broder, S.
AU - Jaffe, E. S.
AU - Gelmann, E.
AU - Blattner, W.
AU - Lofters, W.
AU - Young, R. C.
N1 - Funding Information:
I Received May 31, 1984; accepted August 18, 1984. 2Cytogenetic Oncology Section, Medicine Branch, Division of Cancer Treatment, National Cancer Institute (NCI), National Institutes of Health, Public Health Service, U.S. Department of Health and Human Services, Bethesda, MD 20205. 3 Address reprint requests to Dr. Whang-Peng, Building 10, Room 12N-226, National Institutes of Health, Bethesda, MD 20205. 1 NCI-Navy Medical Oncology Branch, Division of Cancer Treatment, NCI. 5 Clinical Oncology Program, Division of Cancer Treatment, NCI. fi Laboratory of Pathology, Division of Cancer Biology and Diagnosis, NCI. 7 Medicine Branch, Division of Cancer Treatment, NCI. 8 Epidemiology and Biostatistics Program, Division of Cancer Etiology, NCI. 9 Department of Pathology, University of West Indies, Kingston, Jamaica. 10Laboratory of Tumor Cell Biology, Division of Cancer Treatment, NCI.
PY - 1985
Y1 - 1985
N2 - Cytogenetic studies were conducted on fresh and cultured cells from 11 patients with human T-cell leukemia virus-associated adult T cell leukemia-lymphoma. Clones with abnormal karyotypes were detected in 9 of the 11 patients. Chromosome numbers were near-diploid in cells from all but 1 patient who also had a tetraploid clone. The chromosome abnormalities in these cells were extensive; numerous complex structural changes were seen in every chromosome pair. Structural abnormalities occurred frequently in chromosome 6. The 6 patients with chromosome 6 deletions had breakpoints at bands q11, q13, q16q23, q21q23, q22q24, and q23q24. The characteristic clinical features of these 6 patients were aggressive course, short survival, poor response to chemotherapy, high white blood cell counts, hypercalcemia, and bone lesions, whereas cytogenetically abnormal patients without chromosome 6q deletions tended to have a more indolent course. The precise role of the 6q deletion cannot be established with certainty from these data. However, this abnormality appears to occur with a greater than expected frequency in this large cell aggressive lymphoma, in association with hypercalcemia and lytic bone lesions.
AB - Cytogenetic studies were conducted on fresh and cultured cells from 11 patients with human T-cell leukemia virus-associated adult T cell leukemia-lymphoma. Clones with abnormal karyotypes were detected in 9 of the 11 patients. Chromosome numbers were near-diploid in cells from all but 1 patient who also had a tetraploid clone. The chromosome abnormalities in these cells were extensive; numerous complex structural changes were seen in every chromosome pair. Structural abnormalities occurred frequently in chromosome 6. The 6 patients with chromosome 6 deletions had breakpoints at bands q11, q13, q16q23, q21q23, q22q24, and q23q24. The characteristic clinical features of these 6 patients were aggressive course, short survival, poor response to chemotherapy, high white blood cell counts, hypercalcemia, and bone lesions, whereas cytogenetically abnormal patients without chromosome 6q deletions tended to have a more indolent course. The precise role of the 6q deletion cannot be established with certainty from these data. However, this abnormality appears to occur with a greater than expected frequency in this large cell aggressive lymphoma, in association with hypercalcemia and lytic bone lesions.
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M3 - Article
C2 - 2983135
AN - SCOPUS:0021963102
SN - 0027-8874
VL - 74
SP - 357
EP - 369
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 2
ER -