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不同治疗方式后继发性白血病/骨髓增生异常综合征患者的细胞遗传学研究

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

作者信息

Whang-Peng J, Young R C, Lee E C, Longo D L, Schechter G P, DeVita V T

机构信息

Medicine Branch, National Cancer Institute, Bethesda, MD 20892.

出版信息

Blood. 1988 Feb;71(2):403-14.

PMID:3337904
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.

摘要

对68例在接受广泛化疗和/或放疗后发生继发性白血病(SL)/骨髓增生异常综合征(DMS)的患者以及未接受此类治疗而发生SL/DMS的患者进行的细胞遗传学研究表明,那些单独接受放疗或同时接受化疗的患者比仅接受化疗的患者有更广泛的数目和结构异常。就具体的染色体异常而言,各治疗组之间没有差异。亚二倍体是这些患者中最常见的非整倍体形式,最常见的数目异常是7号染色体缺失。最常见的结构异常涉及3号和5号染色体。与原发性白血病和DMS患者相比,这些患者的染色体异常更复杂、更广泛。系列研究显示,细胞遗传学异常在血液学变化发生之前并没有显著的时间间隔。

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