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METHOD FOR DETERMINING CLINICAL EFFECTIVENESS IN B-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA

机译:测定B细胞慢性淋巴细胞白血病临床疗效的方法

摘要

FIELD: medicine.;SUBSTANCE: invention can be used for monitoring the clinical antitumour effectiveness in patients suffering B-cell chronic lymphocytic leukaemia. For this purpose, CD20-positive B-cells are measured in the peripheral blood after a therapeutic course. That is combined with determining a mean activity of CB20 antigen fluorescence on B-lymphocytes, as well as the CD25-positive B-cell count. If the measured CD20-positive B-cell count falls within the range of 0 to 20%, while the CD25-positive B-cell count is from 0 to 20% with the mean CB20 antigen fluorescence intensity of 150 standard units or more, the treatment appears to be effective. The CD20-positive B-cell and CD25-positive B-cell counts exceeding 20% with the mean CB20 antigen fluorescence intensity of less than 150 standard unit show the non-effective treatment.;EFFECT: using the given method enables stating the efficacy of the conduced therapeutic regimens at the earlier stages of the disease, before any clinical manifestations that offers a clinician the possibility to correct the therapeutic approach in good time, and reduces the rate of potential complications of using the new preparations.;3 ex, 6 dwg
机译:领域:药物;发明:本发明可用于监测患有B细胞慢性淋巴细胞性白血病的患者的临床抗肿瘤效力。为此,在治疗过程后在外周血中测量CD20阳性B细胞。这与确定CB20抗原荧光在B淋巴细胞上的平均活性以及CD25阳性B细胞计数结合在一起。如果测得的CD20阳性B细胞计数在0至20%的范围内,而CD25阳性B细胞计数在0至20%之间,且平均CB20抗原荧光强度为150个标准单位或以上,则治疗似乎是有效的。 CD20阳性B细胞和CD25阳性B细胞计数超过20%,且平均CB20抗原荧光强度低于150个标准单位时显示无效;;效果:使用给定的方法可以说明治疗的有效性在疾病的较早阶段进行的治疗方案,在任何临床表现之前都可以为临床医生提供及时纠正治疗方法的可能性,并减少使用新制剂的潜在并发症发生率。3ex,6 dwg

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