Han T, Henderson E S, Emrich L J, Sandberg A A
Department of Medical Oncology, Roswell Park Memorial Institute, Buffalo, NY 14263.
Semin Hematol. 1987 Oct;24(4):257-63.
Cytogenetic analyses by G-banding and/or Q-banding techniques of leukemic B cells were performed in 102 patients with chronic lymphocytic leukemia (CLL), including six with prolymphocytic leukemia (PLL), one with hairy cell leukemia (HCL), and one with Waldenstrom's macroglobulinemia (WM) from 1979 through 1983. Follow-up after cytogenetic study ranged from 24 to 70 months. Seventeen patients had stage 0, 10 had stage I, 31 had stage II, and 44 had stage III or IV. Adequate metaphases were obtained for karyotypic analysis in 86 (84%) of 102 patients. Of these 86 patients with adequate metaphases, 43 had normal karyotypes (50%) and 43 had abnormal karyotypes (50%), of which trisomy 12 was the most frequent. Ten patients had trisomy 12 as the sole abnormality, 14 had trisomy 12 in combination with other abnormalities, and the remaining 19 had other abnormalities without trisomy 12. Abnormal karyotypes were more frequently associated with patients with advanced stages than those with early stages of the disease. Response rate to chemotherapy was significantly higher in patients with normal karyotypes than in those with abnormal karyotypes. Of eight patients who subsequently developed Richter's syndrome, seven initially had complex karyotypic changes with or without trisomy 12. These observations suggest that the chances of development of Richter's syndrome in CLL patients with multiple chromosome changes may be much higher than in those with either simple trisomy 12 or a normal karyotype. Mean frequency of abnormal metaphases was significantly higher in patients with complex trisomy 12 in combination with other changes than in those with trisomy 12 as the sole abnormality.(ABSTRACT TRUNCATED AT 250 WORDS)
1979年至1983年期间,对102例慢性淋巴细胞白血病(CLL)患者进行了白血病B细胞的G显带和/或Q显带细胞遗传学分析,其中包括6例幼淋巴细胞白血病(PLL)、1例毛细胞白血病(HCL)和1例瓦尔登斯特伦巨球蛋白血症(WM)患者。细胞遗传学研究后的随访时间为24至70个月。17例患者为0期,10例为I期,31例为II期,44例为III期或IV期。102例患者中有86例(84%)获得了用于核型分析的足够中期分裂相。在这86例有足够中期分裂相的患者中,43例核型正常(50%),43例核型异常(50%),其中12号染色体三体最为常见。10例患者以12号染色体三体为唯一异常,14例患者12号染色体三体合并其他异常,其余19例患者有其他异常但无12号染色体三体。核型异常在疾病晚期患者中比早期患者更常见。核型正常的患者对化疗的反应率明显高于核型异常的患者。在随后发生里氏综合征的8例患者中,7例最初有复杂的核型改变,伴有或不伴有12号染色体三体。这些观察结果表明,有多种染色体改变的CLL患者发生里氏综合征的可能性可能比单纯12号染色体三体或核型正常的患者高得多。与以12号染色体三体为唯一异常的患者相比,12号染色体三体合并其他改变的复杂三体患者异常中期分裂相的平均频率明显更高。(摘要截短于250字)