Mackintosh W, Richards J D, Jacobs P
S Afr Med J. 1985 Mar 23;67(12):450-2.
Of 27 consecutive adult patients with acute lymphoblastic leukaemia (ALL), 7 had T-cell variants on the basis of sheep erythrocyte (E) rosette formation; in 5, a characteristic thymic phenotype was demonstrated by the use of appropriate monoclonal antibodies. All patients were treated with prednisone, vincristine, 1-asparaginase and adriamycin and the peripheral blood cleared of circulating lymphoblasts in a median of 8 days (range 6 - 45 days), a figure which does not differ significantly from that of 7 days (range 3 - 59 days) in those with the common ALL (P greater than 0,5). The complete remission rates were 71% for the patients with T-cell leukaemia and 75% for the E rosette-negative patients; median durations of remission were 35 and 26 weeks respectively and the actuarially predicted median durations of survival were 49 and 39 weeks respectively. Therefore the presence of T-cell markers in adult ALL does not seem to affect the prognosis in the same way that it does in children, and this is likely to be the result of the more aggressive clinical course of ALL of all phenotypes in adults.
在27例连续性成年急性淋巴细胞白血病(ALL)患者中,7例基于绵羊红细胞(E)花环形成具有T细胞变异型;5例通过使用合适的单克隆抗体表现出特征性胸腺表型。所有患者均接受泼尼松、长春新碱、L-天冬酰胺酶和阿霉素治疗,外周血中循环淋巴母细胞清除的中位时间为8天(范围6 - 45天),这一数值与普通ALL患者的7天(范围3 - 59天)相比无显著差异(P>0.5)。T细胞白血病患者的完全缓解率为71%,E花环阴性患者为75%;缓解期的中位持续时间分别为35周和26周,精算预测的中位生存期分别为49周和39周。因此,成人ALL中T细胞标志物的存在似乎并不像在儿童中那样影响预后,这可能是成人所有表型ALL临床病程更具侵袭性的结果。