Powles R L, Selby P J, Palu G, Morgenstern G, McElwain T J, Clink H M, Alexander P
Lancet. 1979 Sep 29;2(8144):674-6. doi: 10.1016/s0140-6736(79)92070-1.
15 patients with acute myeloblastic leukaemia (AML) in remission were given immunotherapy and 17 similar patients were given immunotherapy plus chemotherapy with the drugs used to induce remission. Median remission length was 245 days for both groups and median survival was 465 days for patients given chemoimmunotherapy and 476 days for patients given only immunotherapy. The failure of remission chemotherapy in AML cannot be attributed to induced resistance because the same drugs induced a second remission in 60% of the patients. From laboratory studies with human AML cells it is suggested that in AML the residual leukaemic cells mature after induction chemotherapy and are then refractory to further drug treatment. Relapse occurs when the leukaemic population proliferates and the environment permits dedifferentiation into frank blast cells.
15例处于缓解期的急性髓细胞白血病(AML)患者接受了免疫治疗,17例相似患者接受了免疫治疗加用于诱导缓解的化疗药物。两组的中位缓解期均为245天,接受化疗免疫治疗的患者中位生存期为465天,仅接受免疫治疗的患者中位生存期为476天。AML缓解化疗的失败不能归因于诱导耐药,因为相同的药物在60%的患者中诱导了第二次缓解。从对人AML细胞的实验室研究表明,在AML中,残留的白血病细胞在诱导化疗后成熟,然后对进一步的药物治疗产生耐药。当白血病细胞群体增殖且环境允许去分化为原始母细胞时,就会发生复发。