Serviço de Hematologia, Instituto Português de Oncologia de Lisboa, Francisco Gentil, Lisbon, Portugal.
Ann Hematol. 2013 Sep;92(9):1201-6. doi: 10.1007/s00277-013-1762-9. Epub 2013 Apr 21.
Higher-risk myelodysplastic syndromes (MDS) are aggressive disorders with rapid progression to AML and short survival. Azacitidine has shown unprecedented survival advantage in these patients but its treatment schedule involves daily hospital administrations for 7 days every 4 weeks. Due to patient and staffing constraints, we have treated 50 patients with a 5-day dose-intensified (500 mg/m(2) total monthly dose divided in 5 days) azacitidine schedule in our center. The regimen was well tolerated, with Grade 3/4 adverse events seen in 24 % patients and only two discontinuations due to toxicity. The response rate was similar to that reported with the 7-day schedule: 16 % complete remissions, 32 % partial remissions, and 62 % transfusion independence. The median survival was 19.2 months from diagnosis. In addition, this regimen reduced hospital visits by 28 % and drug use by 30 %. Our results demonstrate the safety and efficacy of a dose-intensified 5-day regimen.
高风险骨髓增生异常综合征(MDS)是一种侵袭性疾病,迅速进展为急性髓系白血病(AML),患者生存时间短。阿扎胞苷在这些患者中显示出前所未有的生存优势,但它的治疗方案涉及每周 7 天,每天在医院接受治疗,每 4 周为一个疗程。由于患者和人员的限制,我们中心对 50 例患者采用了 5 天剂量强化(每月总剂量 500mg/m2,5 天内分剂量给予)阿扎胞苷方案进行治疗。该方案耐受性良好,3/4 级不良事件发生率为 24%,仅有 2 例因毒性而停药。该方案的缓解率与 7 天方案相似:完全缓解率为 16%,部分缓解率为 32%,输血独立性为 62%。从诊断到中位生存期为 19.2 个月。此外,该方案还减少了 28%的住院次数和 30%的药物使用。我们的结果表明,强化剂量 5 天方案是安全有效的。