From the Center for Cancer Research, National Cancer Institute, Bethesda, MD.
N Engl J Med. 2013 Nov 14;369(20):1915-25. doi: 10.1056/NEJMoa1308392.
Burkitt's lymphoma is an aggressive B-cell lymphoma that occurs in children and adults and is largely curable with the use of intensive and toxic chemotherapy. Current treatments are less effective and have more severe side effects in adults and patients with immunodeficiency than in children.
We studied low-intensity treatment consisting of infused etoposide, doxorubicin, and cyclophosphamide with vincristine, prednisone, and rituximab (EPOCH-R) in patients with untreated Burkitt's lymphoma. Two EPOCH-R regimens were tested: a standard dose-adjusted combination in human immunodeficiency virus (HIV)-negative patients (DA-EPOCH-R group) and a lower-dose short-course combination with a double dose of rituximab in HIV-positive patients (SC-EPOCH-RR group).
A total of 30 consecutive patients were treated; 19 patients were in the DA-EPOCH-R group, and 11 in the SC-EPOCH-RR group. The overall median age of the patients was 33 years, and 40% were 40 years of age or older; 73% of the patients had intermediate-risk disease, and 10% had high-risk disease. The principal toxic events, fever and neutropenia, were observed during 22% of the DA-EPOCH-R treatment cycles and 10% of the SC-EPOCH-RR treatment cycles. The tumor lysis syndrome developed in 1 patient; no treatment-related deaths occurred. The median cumulative doses of doxorubicin-etoposide and cyclophosphamide administered in the SC-EPOCH-RR group were 47% and 57% lower, respectively, than those administered in the DA-EPOCH-R group. With median follow-up times of 86 months in the DA-EPOCH-R group and 73 months in the SC-EPOCH-RR group, the rates of freedom from progression of disease and overall survival were, respectively, 95% and 100% with DA-EPOCH-R and 100% and 90% with SC-EPOCH-RR. None of the patients died from Burkitt's lymphoma.
In this uncontrolled prospective study, low-intensity EPOCH-R-based treatment was highly effective in adults with sporadic or immunodeficiency-associated Burkitt's lymphoma. (Funded by the National Cancer Institute; ClinicalTrials.gov numbers, NCT00001337 and NCT00006436.).
伯基特淋巴瘤是一种侵袭性 B 细胞淋巴瘤,可发生于儿童和成人,通过使用强化和有毒的化疗,大多数患者可被治愈。目前的治疗方法在成人和免疫缺陷患者中的效果较差,且副作用更严重,不如在儿童中有效。
我们研究了未经治疗的伯基特淋巴瘤患者接受低强度治疗,包括依托泊苷、多柔比星和环磷酰胺联合长春新碱、泼尼松和利妥昔单抗(EPOCH-R)。我们测试了两种 EPOCH-R 方案:一种是在 HIV 阴性患者中使用标准剂量调整的组合(DA-EPOCH-R 组),另一种是在 HIV 阳性患者中使用低剂量短疗程组合并加倍利妥昔单抗(SC-EPOCH-RR 组)。
共治疗了 30 例连续患者;19 例患者在 DA-EPOCH-R 组,11 例患者在 SC-EPOCH-RR 组。患者的中位年龄为 33 岁,40%的患者年龄在 40 岁或以上;73%的患者为中危疾病,10%的患者为高危疾病。主要毒性事件,发热和中性粒细胞减少,分别发生在 22%的 DA-EPOCH-R 治疗周期和 10%的 SC-EPOCH-RR 治疗周期。1 例患者发生肿瘤溶解综合征;无治疗相关死亡。在 SC-EPOCH-RR 组中,阿霉素-依托泊苷和环磷酰胺的累积剂量分别降低了 47%和 57%,低于 DA-EPOCH-R 组。在 DA-EPOCH-R 组的中位随访时间为 86 个月,在 SC-EPOCH-RR 组的中位随访时间为 73 个月,无疾病进展的生存率和总生存率分别为 DA-EPOCH-R 组的 95%和 100%,SC-EPOCH-RR 组的 100%和 90%。没有患者死于伯基特淋巴瘤。
在这项未对照的前瞻性研究中,基于低强度 EPOCH-R 的治疗在患有散发性或免疫缺陷相关伯基特淋巴瘤的成人中非常有效。(由美国国立癌症研究所资助;临床试验.gov 编号,NCT00001337 和 NCT00006436。)。