Hann I M, Eden O B, Barnes J, Pinkerton C R
Department of Haematology and Oncology, Hospitals for Sick Children, London.
Br J Haematol. 1990 Nov;76(3):359-64. doi: 10.1111/j.1365-2141.1990.tb06368.x.
An intensive 6-month schedule of drugs was devised with both systemic and central nervous system activity, known by the acronym 'MACHO', to treat 24 newly and consecutively diagnosed children, 13 with stage IV B-cell non-Hodgkin's lymphoma (B-NHL) and 11 with B-cell acute lymphoblastic leukaemia (B-ALL). There were three deaths from complications of chemotherapy (two infective, one biochemical). Five children with central nervous system disease at diagnosis (CNS+) received planned additional megatherapy/bone marrow transplants. Event-free survival (EFS) at 1 year for the 11 cases of B-ALL is 64% (95% confidence intervals [CI] 31-89%) and of 13 stage IV B-NHL cases is 50% (95% CI 19-75%). Patients with bulky abdominal disease had a 32% EFS at 1 year (CI 13-68%) compared with 76% (CI 39-94%) for those without bulky abdominal disease. Overall EFS for eight CNS+ patients is 73% at 1 year (95% CI 34-97%) compared with 48% (95% 24-74%) for those without CNS disease (CNS-). However, only two of the CNS+ cases had bulky abdominal disease (patients 10 and 12) and the difference is not significant (P less than 0.5). A score of 1 was given for each of the following potential prognostic features: bulky abdominal disease, pleural effusion and severe renal dysfunction within 48 h of presentation. Patients who scored 0 or 1 fared significantly better than those who scored 2 or 3 (EFS at 1 year 78% [CI 49-95%] versus 24% [6-65%], P less than 0.04). Two patients with a score of 2 survived past 6 months and another is currently well, but has not regenerated his marrow following autologous transplantation. This protocol is relatively effective for patients who have B-ALL, but those patients who have bulky abdominal disease, often associated with severe renal dysfunction, and those with CNS disease, do not fare so well and require new approaches to therapy.
制定了一个为期6个月的强化药物治疗方案,该方案具有全身和中枢神经系统活性,简称为“MACHO”,用于治疗24例新诊断且连续入组的儿童,其中13例为IV期B细胞非霍奇金淋巴瘤(B-NHL),11例为B细胞急性淋巴细胞白血病(B-ALL)。化疗并发症导致3例死亡(2例感染性,1例生化性)。5例诊断时伴有中枢神经系统疾病(CNS+)的儿童接受了计划中的额外大剂量治疗/骨髓移植。11例B-ALL病例1年时的无事件生存率(EFS)为64%(95%置信区间[CI]31-89%),13例IV期B-NHL病例为50%(95%CI 19-75%)。有巨大腹部肿块的患者1年时的EFS为32%(CI 13-68%),而无巨大腹部肿块的患者为76%(CI 39-94%)。8例CNS+患者1年时的总体EFS为73%(95%CI 34-97%),而无CNS疾病(CNS-)的患者为48%(95%CI 24-74%)。然而,CNS+病例中只有2例有巨大腹部肿块(患者10和12),差异无统计学意义(P小于0.5)。对于以下每个潜在的预后特征各计1分:巨大腹部肿块、胸腔积液和就诊后48小时内严重肾功能不全。得分为0或1的患者预后明显好于得分为2或3的患者(1年时的EFS为78%[CI 49-95%]对24%[6-65%],P小于0.04)。2例得分为2的患者存活超过6个月,另1例目前情况良好,但自体移植后骨髓未再生。该方案对B-ALL患者相对有效,但有巨大腹部肿块(常伴有严重肾功能不全)的患者以及有CNS疾病的患者预后不佳,需要新的治疗方法。