van Geel B M, Huijgens P C, Ossenkoppele G J, Wijermans P W, Langenhuijsen M M
Neth J Med. 1989 Oct;35(3-4):128-36.
In this retrospective study, 61 induction treatment periods in 57 patients with myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML) were evaluated. According to the WHO performance status, 6 patients received no chemotherapy, 20 had low dose cytosine arabinoside (LD ara-C) induction courses, and 35 received standard induction consisting of daunorubicin and cytosine arabinoside. Untreated patients had a poor survival. Of the 20 patients with LD ara-C induction courses, 4 (20%) achieved complete remission (CR). Three patients (15%) died during induction. Of 35 patients with standard induction, 21 patients (60%) achieved CR. Toxicity was considerable - 11 patients (31%) dying during treatment. We conclude that patients over 60 yr of age with RAEB, RAEB-t or AML had a CR rate and survival comparable to those of younger patients if treated with standard induction chemotherapy at the cost of serious therapy-related complications. In patients who were judged not to be able to tolerate standard induction and who were subsequently treated with LD ara-C, complications occurred less frequently, but the CR rate was low and survival short.
在这项回顾性研究中,对57例骨髓增生异常综合征(MDS)或急性髓系白血病(AML)患者的61个诱导治疗期进行了评估。根据世界卫生组织的体能状态,6例患者未接受化疗,20例接受小剂量阿糖胞苷(LD ara-C)诱导疗程,35例接受由柔红霉素和阿糖胞苷组成的标准诱导治疗。未治疗的患者生存率较差。在接受LD ara-C诱导疗程的20例患者中,4例(20%)达到完全缓解(CR)。3例患者(15%)在诱导治疗期间死亡。在35例接受标准诱导治疗的患者中,21例(60%)达到CR。毒性反应相当严重——11例患者(31%)在治疗期间死亡。我们得出结论,60岁以上患有难治性贫血伴原始细胞增多(RAEB)、难治性贫血伴原始细胞增多转变型(RAEB-t)或AML的患者,如果接受标准诱导化疗,其CR率和生存率与年轻患者相当,但代价是会出现严重的治疗相关并发症。对于那些被判定无法耐受标准诱导治疗且随后接受LD ara-C治疗的患者,并发症发生频率较低,但CR率低且生存期短。