Bogusławska-Jaworska J, Raus Z
Arch Immunol Ther Exp (Warsz). 1981;29(6):719-23.
Thirty seven children with acute lymphoblastic leukemia (All) treated according to 2 different protocols were randomized after remission induction to receive levamisole or not during remission maintenance continuous or intermittent polychemotherapy. The usefulness of levamisole in prolonged remission and survival time by the actuarial analysis were studied. At 36th month 45% patients treated with levamisole, and 30% without levamisole remained in complete remission. The increase of E+ lymphocyte and total lymphocyte count in the 18th week of chemoimmunotherapy, and their decrease in 27th week of the treatment were demonstrated. The granulocyte phagocytic activity increased in the 27th week of treatment. The results obtained suggest that levamisole therapy stimulates T lymphocyte production and phagocytic activity and enables the appropriate cytostatic treatment.
37名急性淋巴细胞白血病(ALL)患儿按照2种不同方案进行治疗,在诱导缓解后随机分组,在缓解期维持阶段接受持续或间歇多药化疗时使用或不使用左旋咪唑。通过精算分析研究了左旋咪唑在延长缓解期和生存时间方面的有效性。在第36个月时,接受左旋咪唑治疗的患者中有45%仍处于完全缓解状态,未接受左旋咪唑治疗的患者中这一比例为30%。化疗免疫治疗第18周时E +淋巴细胞和总淋巴细胞计数增加,而在治疗第27周时减少。治疗第27周时粒细胞吞噬活性增加。所得结果表明,左旋咪唑治疗可刺激T淋巴细胞生成和吞噬活性,并使适当的细胞抑制治疗成为可能。