Sessarego M, Frassoni F, Defferrari R, Bacigalupo A, Miceli S, Mareni C, Ajmar F
Cattedra di Clinica Medica, Università di Genova, Italy.
Cancer Genet Cytogenet. 1989 Oct 15;42(2):253-61. doi: 10.1016/0165-4608(89)90093-9.
Forty-eight consecutive patients affected by chronic myelogenous leukemia (CML) Philadelphia (Ph) chromosome positive during the chronic phase of the disease underwent allogeneic bone marrow transplantation (BMT). Thirty-five patients had a follow-up over 12 months and were included in a cytogenetic study in order to evaluate the Ph clone eradication. In 25 cases, the Ph chromosome disappeared in all cytogenetic studies, and their hematologic picture is at present apparently normal. Ten patients showed cytogenetic relapse. In one case, the cytogenetic relapse was transitory without any clinical sign of the disease; in three cases, after a transitory cytogenetic relapse, a persistent relapse with clinical picture of progression of the disease occurred; in six cases cytogenetic and a clinical relapse were coincident. Structural chromosomal abnormalities other than Ph were temporarily seen in three cases. The so-called "nonrandom" chromosomal changes typical of the blastic phase were never detected. The reappearing Ph-positive clone spontaneously disappeared in three patients, and their hematologic picture reverted to complete chimerism. The present study confirms that the eradication of the Ph clone is often defective with BMT, and cytogenetic analysis can detect the competition between donor and residual host marrow. Furthermore, the karyotype evolution is different from that found in CML patients treated with conventional chemotherapy.
48例慢性粒细胞白血病(CML)慢性期费城(Ph)染色体阳性患者接受了异基因骨髓移植(BMT)。35例患者随访超过12个月,并纳入细胞遗传学研究以评估Ph克隆的清除情况。在25例中,所有细胞遗传学研究中Ph染色体均消失,其血液学表现目前明显正常。10例患者出现细胞遗传学复发。1例患者细胞遗传学复发为短暂性,无任何疾病临床体征;3例患者在短暂性细胞遗传学复发后,出现疾病进展临床表现的持续性复发;6例患者细胞遗传学和临床复发同时出现。3例患者暂时出现除Ph以外的结构性染色体异常。从未检测到典型的急变期“非随机”染色体改变。3例患者中再次出现的Ph阳性克隆自发消失,其血液学表现恢复为完全嵌合状态。本研究证实,BMT对Ph克隆的清除往往存在缺陷,细胞遗传学分析可检测供体与残留宿主骨髓之间的竞争。此外,核型演变与接受传统化疗的CML患者不同。