Tilly H, Castaigne S, Bordessoule D, Casassus P, Le Prisé P Y, Tertian G, Desablens B, Henry-Amar M, Degos L
Centre Henri Becquerel, Rouen, France.
J Clin Oncol. 1990 Feb;8(2):272-9. doi: 10.1200/JCO.1990.8.2.272.
We conducted a randomized multicenter trial comparing low-dose cytarabine (LD ARA-C) (20 mg/m2 for 21 days) with an intensive chemotherapy (rubidazone [a daunorubicin-derived agent], 100 mg/m2 for 4 days, ARA-C 200 mg/m2 for 7 days) in 87 patients over 65 years of age with de novo acute nonlymphocytic leukemia (ANLL). Forty-one patients received LD ARA-C and 46 received intensive chemotherapy. The number of complete remissions (CRs) but also of early deaths was higher in the intensive chemotherapy group, while partial remissions (PRs) and failures were more frequent in the LD ARA-C group (P less than .001). Infectious complications during induction treatment were more numerous and more severe in the intensive chemotherapy group (P less than .01). Patients treated with LD ARA-C required fewer RBC transfusions (P less than .02), fewer platelet transfusions (P less than .01), and had a shorter hospital stay for induction treatment (P less than .01). Overall survival and CR duration were not significantly different in either group. In the LD ARA-C group, the survival of patients with PR and those of patients in CRs was identical. We conclude that in a selected group of elderly patients with de novo ANLL a higher number of CRs may be obtained with intensive chemotherapy, but that with LD ARA-C, the number of early deaths is lower, and long-lasting PRs are obtained, resulting in a similar overall survival.
我们开展了一项随机多中心试验,在87例65岁以上的初发急性非淋巴细胞白血病(ANLL)患者中,比较小剂量阿糖胞苷(LD ARA-C)(20 mg/m²,共21天)与强化化疗(柔红霉素腙[一种柔红霉素衍生剂],100 mg/m²,共4天,阿糖胞苷200 mg/m²,共7天)的疗效。41例患者接受LD ARA-C治疗,46例接受强化化疗。强化化疗组的完全缓解(CR)数以及早期死亡数均较高,而LD ARA-C组部分缓解(PR)和治疗失败更为常见(P<0.001)。强化化疗组诱导治疗期间的感染并发症更多且更严重(P<0.01)。接受LD ARA-C治疗的患者需要的红细胞输注较少(P<0.02),血小板输注较少(P<0.01),诱导治疗的住院时间较短(P<0.01)。两组的总生存期和CR持续时间无显著差异。在LD ARA-C组,PR患者与CR患者的生存期相同。我们得出结论,在一组选定的初发ANLL老年患者中,强化化疗可能获得更多的CR,但LD ARA-C治疗早期死亡数较低,可获得持久的PR,从而使总生存期相似。