Monitoring the therapy of acute lymphoid leukemia (ALL) in children--changes induced in clinical, cytological and immunological parameters during treatment of high malignancy ALL with ALL-BFM 88.

Acta paediatrica Hungarica Pub Date : 1992-01-01
M Babosa
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Abstract

The ALL-BFM 88 RF greater than 1.7 treatment of high malignancy ALL patients in remission was monitored at the 4th week of Protocol I. The qualitative and quantitative processing of parameters indicating cellular transformations by light and electronmicroscopy was performed in lymphocytes separated from peripheral blood drawn at scheduled times of therapy. The immunophenotype of sample lymphocytes was determined by indirect immunofluorescent techniques, by listing the percentual level of CD2, CD3, CD4, CD8, CD19 surface antigens. The incidence of infections, confirmed clinically and bacteriologically, was recorded. The parameters of the patients were compared to those of healthy children. In the group of patients with high malignancy in the intensive period of ALL-BFM 88 RF greater than 1.7 therapy the incidence of cells rich in organelles, dense granules and vacuoles was significantly (p less than 0.05) higher compared to the control cells, poor in structures. During the weeks of induction and after the consolidating combination with VM-26+ARA-C the expression of surface antigens of the lymphocytes was reduced. That means that up to the introduction of maintenance treatment the presence of surface antigens remained below the range of normal deviation. These data obtained during monitoring revealed that the morphological and functional integrity of cells was damaged in patients with high malignancy ALL during intensive therapy, though only temporarily.

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监测儿童急性淋巴细胞白血病(ALL)的治疗——ALL- bfm 88治疗高恶性ALL期间临床、细胞学和免疫学参数的变化
在方案1的第4周监测缓解期高恶性ALL患者的ALL- bfm 88 RF大于1.7治疗。在预定治疗时间从外周血中分离淋巴细胞,通过光镜和电镜对指示细胞转化的参数进行定性和定量处理。通过列出CD2、CD3、CD4、CD8、CD19表面抗原的百分比水平,采用间接免疫荧光技术测定样品淋巴细胞的免疫表型。记录临床和细菌学证实的感染发生率。将患者的各项参数与健康儿童进行比较。在ALL-BFM - 88射频治疗≥1.7强化期的高恶性肿瘤患者中,细胞器丰富、致密颗粒和液泡丰富、结构差的细胞发生率显著高于对照组(p < 0.05)。在诱导数周内及与VM-26+ARA-C合并后,淋巴细胞表面抗原的表达降低。这意味着,直到引入维持治疗,表面抗原的存在仍然低于正常偏差的范围。在监测期间获得的这些数据显示,高恶性ALL患者在强化治疗期间细胞的形态和功能完整性受到破坏,尽管只是暂时的。
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