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经马法兰治疗的稳定型多发性骨髓瘤患者中的5号染色体长臂3区1带缺失

Deletion 5q31 in patients with stable, melphalan-treated multiple myeloma.

作者信息

Amiel A, Fridman K, Elis A, Gaber E, Manor Y, Fejgin M, Lishner M

机构信息

Department of Medicine, Meir Hospital, Kfar-Saba, Israel.

出版信息

Cancer Genet Cytogenet. 1999 Aug;113(1):45-8. doi: 10.1016/s0165-4608(98)00279-9.

Abstract

The risk of myelodysplastic syndrome (MDS) or acute myeloblastic leukemia (AML) in patients with multiple myeloma has been estimated to be 10-20% after 10 years. Most myeloma patients develop MDS/AML after 3-4 years of treatment with alkylating agents, mainly melphalan; chromosomes 5 and 7 are most frequently involved. We studied 14 patients with myeloma by fluorescence in situ hybridization (FISH) with a probe to 5q31 (the critical area of deletion on chromosome 5) to verify whether deletion of 5q31 occurs during the course of stable, uncomplicated myeloma, and to assess the clinical importance of this abnormality. We found 2 patients (14%) with deletion of 5q31 in 30-40% of their peripheral white blood cells. One patient with this deletion received a high cumulative amount of melphalan, and the other patient was treated with multiple alkylating agents, including melphalan. In these patients, no clinical or laboratory evidence of transformation occurred 14 and 12 months after the finding of the aberration. These findings suggest that 5q-may occur months prior to the overt development of (t)-MDS/AML, and raise important concerns regarding the management of patients with this and similar aberrations, including modification of treatment and performance of cytogenetic evaluation prior to autologous or PSC transplantation. The clinical and biological implications of these findings should be evaluated in larger clinical and laboratory studies.

摘要

据估计,多发性骨髓瘤患者发生骨髓增生异常综合征(MDS)或急性髓细胞白血病(AML)的风险在10年后为10% - 20%。大多数骨髓瘤患者在使用烷化剂(主要是美法仑)治疗3 - 4年后会发生MDS/AML;5号和7号染色体最常受累。我们通过用针对5q31(5号染色体上的关键缺失区域)的探针进行荧光原位杂交(FISH)研究了14例骨髓瘤患者,以验证5q31缺失是否在稳定、无并发症的骨髓瘤病程中出现,并评估这种异常的临床重要性。我们发现2例患者(14%)外周血白细胞中有30% - 40%存在5q31缺失。1例有这种缺失的患者接受了高累积剂量的美法仑,另1例患者接受了包括美法仑在内的多种烷化剂治疗。在这些患者中,发现异常后14个月和12个月均未出现转化的临床或实验室证据。这些发现表明,5q - 可能在(t)- MDS/AML明显发生前数月出现,并引发了对患有这种及类似异常的患者管理的重要关注,包括改变治疗方案以及在自体或PSC移植前进行细胞遗传学评估。这些发现的临床和生物学意义应在更大规模的临床和实验室研究中进行评估。

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