Alimena G, De Cuia M R, Mecucci C, Arcese W, Mauro F, Screnci M, Mancini M, Cedrone M, Nanni M, Montefusco E
Department of Human Biopathology, University of Rome La Sapienza, Italy.
Bone Marrow Transplant. 1990 Feb;5(2):119-27.
Serial cytogenetic studies were carried out on 36 patients with Ph1-positive chronic myelogenous leukemia treated with allogeneic bone-marrow transplantation from unlike sex (21 patients) or like sex (15 patients) donors. Fourteen of the 21 sex-mismatched and 12 of the 15 sex-matched donor marrows were T cell depleted. Disease relapse was documented in 19 of the 26 patients who received T cell-depleted marrow, and in none of the 10 patients who received non-T cell-depleted marrow. In the group of patients with unlike sex donor, a triple donor/normal recipient/Ph1-positive recipient or a double donor/Ph1-positive recipient chimerism was documented during the subsequent months, while on alpha-interferon treatment for relapse. Two of these patients subsequently showed a complete disappearance of the Ph1 chromosome. Unstable and/or stable, clonal or non-clonal chromosome changes were detected in Ph1-positive cells from 12 of the 19 patients who relapsed. Analysis of the identified stable changes showed a non-random distribution of breakpoints with clustering to chromosome nos. 1, 4, 7 and 12.
对36例接受异基因骨髓移植治疗的Ph1阳性慢性粒细胞白血病患者进行了系列细胞遗传学研究,供体为不同性别的(21例)或同性别的(15例)。21例性别不匹配和15例性别匹配的供体骨髓中,分别有14例和12例进行了T细胞去除。在接受T细胞去除骨髓的26例患者中,有19例记录到疾病复发,而接受未去除T细胞骨髓的10例患者均未复发。在性别不同供体的患者组中,在随后几个月复发接受α-干扰素治疗期间,记录到三重供体/正常受体/Ph1阳性受体或双重供体/Ph1阳性受体嵌合体。其中两名患者随后显示Ph1染色体完全消失。在19例复发患者的Ph1阳性细胞中,检测到不稳定和/或稳定的、克隆性或非克隆性染色体改变。对所确定的稳定改变的分析显示,断点呈非随机分布,聚集于1、4、7和12号染色体。