Department of Hematology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, PR China.
Myelodysplastic Syndromes Diagnosis and Therapy Center, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, PR China.
Leuk Lymphoma. 2021 Aug;62(8):1920-1929. doi: 10.1080/10428194.2021.1891230. Epub 2021 Mar 7.
Treatment for acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS) ineligible for intensive chemotherapy is a major challenge for clinicians. We enrolled 154 patients ineligible for intensive chemotherapy who were prescribed D-IA regimen (decitabine 15-20 mg/m days 1 to 3-5, followed by idarubicin 3 mg/m for 5-7 days and cytarabine 30 mg/m for 7-14 days). For AML and MDS patients, the overall response rate after two cycles was 66.4% and 76.6%, respectively, and the 2-year overall survival rates were 29% and 31%, respectively. Fourteen (13.1%) AML and five (10.6%) MDS patients underwent allo-HSCT after complete remission. The allo-HSCT group survival time was significantly longer than the control group (median survival time not reached in HSCT group, 13 and 18.5 months in non-HSCT AML and MDS group). We concluded that D-IA regimen was effective and well tolerated for patients with AML or higher-risk MDS ineligible for intensive chemotherapy.
对于不适合强化化疗的急性髓系白血病(AML)和高危骨髓增生异常综合征(MDS)患者,治疗是临床医生面临的主要挑战。我们招募了 154 名不适合强化化疗的患者,给予 D-IA 方案(地西他滨 15-20mg/m2,第 1-3-5 天;随后伊达比星 3mg/m2,第 5-7 天;阿糖胞苷 30mg/m2,第 7-14 天)治疗。对于 AML 和 MDS 患者,两个周期后总体缓解率分别为 66.4%和 76.6%,2 年总生存率分别为 29%和 31%。14 名 AML 患者(13.1%)和 5 名 MDS 患者(10.6%)在完全缓解后接受了异基因造血干细胞移植(allo-HSCT)。allo-HSCT 组的生存时间明显长于对照组(HSCT 组中位生存时间未达到,非 HSCT AML 和 MDS 组分别为 13 和 18.5 个月)。我们得出结论,D-IA 方案对于不适合强化化疗的 AML 或高危 MDS 患者是有效且耐受良好的。