Shimamoto Y, Kikuchi M, Funai N, Suga K, Matsuzaki M, Yamaguchi M
Department of Internal Medicine, Saga Medical School, Japan.
Cancer. 1993 Aug 1;72(3):735-40. doi: 10.1002/1097-0142(19930801)72:3<735::aid-cncr2820720317>3.0.co;2-o.
Spontaneous regression of adult T-cell leukemia/lymphoma (ATL) is considered to be extremely unusual. Of the 82 patients with ATL who the authors saw between 1981 and 1991, spontaneous regression occurred in 3 (3.7%), 2 of whom were previously untreated and one who had been previously treated. Surgical excisional biopsy triggered the spontaneous regression in these patients.
In two of these patients with spontaneous regression, gene analysis studies of human T-cell leukemia virus type I (HTLV-I) proviral DNA, and T-cell receptor (TCR) were carried out by Southern blot analysis in lymph node cells or peripheral lymphocytes before regression and after recurrence.
One patient exhibited monoclonal integration of HTLV-I proviral DNA and the rearranged band of the TCR-beta gene at the same positions both before regression and after recurrence. The other patient showed them at the different positions before regression and after recurrence.
The authors' studies indicated heterogeneity in ATL patients with spontaneous regression. Temporary spontaneous regression could occur in typical ATL and might be associated with a longer survival time than that for prototypic ATL.
成人T细胞白血病/淋巴瘤(ATL)的自发消退被认为极为罕见。在1981年至1991年间作者所诊治的82例ATL患者中,3例(3.7%)出现了自发消退,其中2例既往未接受过治疗,1例曾接受过治疗。手术切除活检引发了这些患者的自发消退。
在其中2例出现自发消退的患者中,在消退前及复发后,通过Southern印迹分析对淋巴结细胞或外周淋巴细胞进行了I型人类T细胞白血病病毒(HTLV-I)前病毒DNA及T细胞受体(TCR)的基因分析研究。
1例患者在消退前及复发后,HTLV-I前病毒DNA的单克隆整合及TCR-β基因的重排条带均位于相同位置。另1例患者在消退前及复发后这些条带位于不同位置。
作者的研究表明,出现自发消退的ATL患者存在异质性。典型ATL可能会出现暂时的自发消退,且与原型ATL相比可能生存期更长。