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治疗与未治疗的骨髓瘤之间骨髓细胞遗传学特征的差异。

Differences in bone marrow cytogenetic characteristics between treated and untreated myeloma.

作者信息

Clark R E, Geddes A D, Whittaker J A, Jacobs A

机构信息

Department of Haematology, University of Wales College of Medicine, Cardiff, U.K.

出版信息

Eur J Cancer Clin Oncol. 1989 Dec;25(12):1789-93. doi: 10.1016/0277-5379(89)90349-0.

Abstract

Clonal karyotypic abnormalities in myelomatosis at initial diagnosis have been widely studied, but little data are available on the karyotypic status following treatment. We have studied bone marrow (BM) from 17 cases of untreated myelomatosis at initial diagnosis and from a further 29 cases who had received chemotherapy with regimens containing alkylating agents. At the time of study all previously treated cases had been off treatment for at least 152 days, had a paraprotein level in plateau phase, had a BM with less than 4% blasts, and in 28 of these 29 cases had less than 20% BM plasma cells. Two cases had more than 15% BM ringed sideroblasts; one other case was transfusion dependent. Clear differences in cytogenetic characteristics between the two groups were seen. At initial diagnosis clonal karyotypic abnormalities were observed in six of 11 accessible cases. All had hyperdiploid clones (of 49-54 chromosomes) and showed characteristic involvement of chromosomes 3, 5, 7, 9, 11, 15, 19 and 21. Additional structural rearrangements were present in only two of these cases. Following treatment, clonal abnormalities were seen in 10 of 25 assessible cases, of which only two showed hyperdiploidy (one with a hyperdiploid line, one with an additional derived chromosome). The remaining eight showed hypodiploid or pseudodiploid lines, and seven of these showed complex karyotypes with multiple rearrangements particularly affecting chromosomes 1, 2, 3, 6 and 7. After a minimum follow-up of 16 months, only four of these 10 cases (40%) remain alive compared with 12 of 15 (80%) with a normal karyotype after treatment (P = 0.03). No correlation was observed between the presence of an abnormal karyotype and the total dose or timing of previous therapy, though cases with an abnormal karyotype tended to have received treatment for longer (790 +/- 166 days) than cases with a normal karyotype (486 +/- 50 days). It is not clear whether the ploidy difference between the two groups represents a change in the disease state due to treatment or a direct effect of treatment itself.

摘要

骨髓瘤初诊时的克隆性核型异常已得到广泛研究,但关于治疗后的核型状态的数据却很少。我们研究了17例初诊时未经治疗的骨髓瘤患者以及另外29例接受过含烷化剂方案化疗的患者的骨髓。在研究时,所有先前接受过治疗的患者已停止治疗至少152天,副蛋白水平处于平台期,骨髓中原始细胞少于4%,在这29例患者中有28例骨髓浆细胞少于20%。2例患者骨髓环形铁粒幼细胞超过15%;另1例患者依赖输血。两组在细胞遗传学特征上存在明显差异。初诊时,11例可评估病例中有6例观察到克隆性核型异常。所有病例均有超二倍体克隆(49 - 54条染色体),并显示出3、5、7、9、11、15、19和21号染色体的特征性受累。这些病例中只有2例存在额外的结构重排。治疗后,25例可评估病例中有10例出现克隆性异常,其中只有2例显示超二倍体(1例为超二倍体系,1例有额外的衍生染色体)。其余8例显示亚二倍体或假二倍体系,其中7例显示复杂核型,有多个重排,尤其影响1、2、3、6和7号染色体。经过至少16个月的随访,这10例患者中只有4例(40%)存活,而治疗后核型正常的15例患者中有12例(80%)存活(P = 0.03)。未观察到异常核型的存在与先前治疗的总剂量或时间之间存在相关性,不过核型异常的病例接受治疗的时间(790±166天)往往比核型正常的病例(486±50天)更长。尚不清楚两组之间的倍性差异是由于治疗导致疾病状态的改变还是治疗本身的直接作用。

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