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PMID: 3337904 Published · ppublish English Journal Article

Cytogenetic studies in patients with secondary leukemia/dysmyelopoietic syndrome after different treatment modalities.

Blood ·Vol. 71 ·No. 2 ·1988-02-00 ·Pages 403-14

Whang-Peng J, Young RC, Lee EC, Longo DL, Schechter GP, DeVita VT

Abstract

Cytogenetic studies of 68 patients who developed secondary leukemia (SL)/dysmyelopoietic syndrome (DMS) after extensive chemotherapy and/or radiation therapy as well as patients who developed SL/DMS without such treatment showed that those patients who received radiation alone or with chemotherapy had more extensive numerical and structural abnormalities than those who received only chemotherapy. In terms of the specific chromosomal abnormalities, there are no differences between the various treatment groups. Hypodiploidy is the most common form of aneuploidy in these patients, with the most common numerical abnormality being the loss of chromosome 7. The most common structural abnormalities involved chromosomes 3 and 5. When compared with patients with de novo leukemia and DMS, the chromosomal abnormalities in these patients are more complex and extensive. Serial studies revealed that cytogenetic abnormalities do not precede the development of hematologic changes by significant time periods.

MeSH Terms
Antineoplastic Agents/adverse effects Chromosome Aberrations/etiology Chromosome Banding Chromosome Disorders Chromosomes, Human, Pair 7 Hodgkin Disease/therapy Humans Leukemia/chemically induced,genetics Leukemia, Radiation-Induced/genetics Lymphoma, Non-Hodgkin/therapy Myeloproliferative Disorders/chemically induced,genetics Time Factors
Chemicals
Antineoplastic Agents
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Whang-Peng J
Medicine Branch, National Cancer Institute, Bethesda, MD 20892.
Young R C
Lee E C
Longo D L
Schechter G P
DeVita V T
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1988-02-00
Pages
403-14
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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