Heyll A, Aul C, Gogolin F, Runde V, Söhngen D, Meckenstock G, Wolf H H, Zahner J, Burk M, Winkelmann M
Klinik für Hämatologie, Onkologie und klinische Immunologie, Universität Düsseldorf, Germany.
Ann Hematol. 1994 Jun;68(6):279-83. doi: 10.1007/BF01695033.
Conventional-dose Ara-C (200 mg/m2 d 1-5) combined with idarubicin (12 mg/m2 d 1-3) was employed as remission induction and consolidation therapy in 23 elderly AML patients with a median age of 66 years (range, 60-75) with AML according to the FAB criteria (M1 n = 3, M2 n = 10, M4 n = 6, M5 n = 2, M6 n = 2), eligible for the study. In seven patients earlier MDS had been documented by previous bone marrow aspirates. The CR rate after one induction course was 65% (15/23). Toxicity was acceptable, with four patients dying during the chemotherapy-induced hypoplasia (4/23). Although 80% of the CR patients received two additional cycles of Ara-C and idarubicin as consolidation therapy, only two patients are still in continuous complete remission more than 12 months after achieving CR. The median disease-free survival of the CR patients was 11.5 months and the median survival of the entire group was 10 months. We conclude that conventional dose Ara-C/idarubicin is an effective protocol for inducing complete remission in elderly patients with AML, but that consolidation therapy consisting of two courses of the same regimen does not produce a relevant rate of long-term disease-free survival.
根据FAB标准(M1 n = 3,M2 n = 10,M4 n = 6,M5 n = 2,M6 n = 2),选取23例年龄中位数为66岁(范围60 - 75岁)的老年急性髓系白血病(AML)患者,采用常规剂量阿糖胞苷(200 mg/m² d 1 - 5)联合伊达比星(12 mg/m² d 1 - 3)进行缓解诱导和巩固治疗,这些患者符合研究条件。7例患者之前的骨髓穿刺检查记录有早期骨髓增生异常综合征(MDS)。一个诱导疗程后的完全缓解(CR)率为65%(15/23)。毒性反应可接受,4例患者在化疗引起的骨髓抑制期死亡(4/23)。尽管80%的CR患者接受了另外两个周期的阿糖胞苷和伊达比星巩固治疗,但只有2例患者在达到CR后持续完全缓解超过12个月。CR患者的无病生存期(DFS)中位数为11.5个月,整个组的总生存期(OS)中位数为10个月。我们得出结论,常规剂量阿糖胞苷/伊达比星是诱导老年AML患者完全缓解的有效方案,但由相同方案的两个疗程组成的巩固治疗并不能产生显著的长期无病生存率。