Metabolism Branch, National Cancer Institute, Bethesda, MD 20892, USA.
Haematologica. 2012 May;97(5):758-65. doi: 10.3324/haematol.2011.056531. Epub 2011 Dec 1.
A phase II trial of dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin and rituximab (DA-EPOCH-R) from the National Cancer Institute showed promising activity in untreated diffuse large B-cell lymphoma. The Cancer and Leukemia Group B conducted a study to determine if these results could be reproduced in a multi-institutional setting.
The study included 69 patients with untreated diffuse large B-cell lymphoma at least 18 years of age and at least stage II. Radiaton therapy was not permitted on study. Median age was 58 years (range 23-83) and 40% had high-intermediate or high International Prognostic Index risk. Immunohistochemical biomarkers for cell of origin and proliferation were performed.
With a median follow up of 62 months, time to progression and overall survival were 81% and 84%, respectively, and time to progression was 87%, 92% and 54% for low/low-intermediate, high-intermediate and high International Prognostic Index risk groups, respectively, at 5-years and beyond. The time to progression and event-free survival of germinal center B-cell lymphoma were 100% and 94%, respectively, and non-germinal center B-cell GCB diffuse large B-cell lymphoma were 67% and 58%, respectively, at 62 months (germinal center vs. non-germinal center B cell P=0.008). DA-EPOCH-R was tolerated without significant grade 4 non-hematologic toxicities.
These results provide the first confirmation by a multi-institutional group that DA-EPOCH-R provides high durable remissions in diffuse large B-cell lymphoma and is effective in both germinal center and non-germinal center B-cell subtypes. The trial was registered at ClinicalTrials.Gov (NCT00032019).
美国国家癌症研究所进行的一项 II 期试验表明,剂量调整的依托泊苷、泼尼松、长春新碱、环磷酰胺、多柔比星和利妥昔单抗(DA-EPOCH-R)在未经治疗的弥漫性大 B 细胞淋巴瘤中具有良好的疗效。癌症和白血病组 B 进行了一项研究,以确定这些结果是否可以在多机构环境中重现。
该研究纳入了 69 名年龄至少 18 岁且至少为 II 期的未经治疗的弥漫性大 B 细胞淋巴瘤患者。研究中不允许进行放射治疗。中位年龄为 58 岁(范围 23-83 岁),40%的患者具有高-中或高国际预后指数风险。进行了细胞起源和增殖的免疫组织化学生物标志物检测。
中位随访 62 个月后,无进展生存期和总生存期分别为 81%和 84%,5 年及以上时低/低-中、高-中、高国际预后指数风险组的无进展时间分别为 87%、92%和 54%。生发中心 B 细胞淋巴瘤的无进展时间和无事件生存期分别为 100%和 94%,非生发中心 B 细胞 GCB 弥漫性大 B 细胞淋巴瘤分别为 67%和 58%,在 62 个月时(生发中心与非生发中心 B 细胞,P=0.008)。DA-EPOCH-R 可耐受,无明显 4 级非血液学毒性。
这些结果首次由多机构组证实,DA-EPOCH-R 可使弥漫性大 B 细胞淋巴瘤获得高持久缓解,并且在生发中心和非生发中心 B 细胞亚型中均有效。该试验在 ClinicalTrials.Gov 注册(NCT00032019)。