Arch Dis Child. 1985 Nov;60(11):1050-4. doi: 10.1136/adc.60.11.1050.
Eighty two eligible children with 'standard risk' lymphoblastic leukaemia were entered into the Medical Research Council UKALL VII trial. Three failed to remit. With a minimum follow up time of four years, actuarial relapse free survival for the remainder was 65%; a significant improvement over the two preceding 'standard risk' trials at the same stage. Only one of five treatment variables possibly affected relapse free survival; this being whether methotrexate was given orally or parenterally during remission maintenance treatment. Twenty seven of 36 patients (75%) who were given intramuscular methotrexate remain alive and in their first remission compared with 23 of 41 (56%) given the drug orally. Although statistically significant differences in small trials should be interpreted with caution, this finding raises the possibility that orally administered methotrexate is not completely absorbed.
82名符合条件的“标准风险”淋巴细胞白血病患儿参加了英国医学研究委员会的UKALL VII试验。3名患儿未缓解。在至少4年的随访时间里,其余患儿的无复发生存率为65%;与之前两个同阶段的“标准风险”试验相比有显著改善。五个治疗变量中只有一个可能影响无复发生存率;这一变量是在缓解期维持治疗期间甲氨蝶呤是口服还是肠外给药。接受肌肉注射甲氨蝶呤的36名患者中有27名(75%)仍然存活且处于首次缓解期,而口服该药的41名患者中有23名(56%)处于首次缓解期。尽管在小型试验中具有统计学意义的差异应谨慎解读,但这一发现增加了口服甲氨蝶呤未被完全吸收的可能性。