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初诊高肿瘤负荷惰性非霍奇金淋巴瘤的硼替佐米联合利妥昔单抗一线治疗:一项多中心 II 期研究。

Frontline bortezomib and rituximab for the treatment of newly diagnosed high tumour burden indolent non-Hodgkin lymphoma: a multicentre phase II study.

机构信息

Division of Hematology/Oncology, Tufts Medical Center, Boston, MA, USA.

出版信息

Br J Haematol. 2014 Aug;166(4):514-20. doi: 10.1111/bjh.12915. Epub 2014 Apr 25.

Abstract

There is a lack of published data examining non-cytotoxic options for the frontline treatment of patients with high-tumour burden (HTB) indolent non-Hodgkin lymphoma (iNHL). We completed a multicentre phase II study for patients with untreated HTB iNHL (NCT00369707) consisting of three induction cycles of weekly bortezomib and rituximab followed by an abbreviated consolidation. Forty-two patients were treated and all were evaluable; the most common histology was follicular lymphoma (FL) (n = 33, 79%). Patient characteristics included median age 62 years (40-86); 38% bulky disease; 19% malignant effusions; 91% advanced-stage disease; and median FL International Prognostic Index (FLIPI) score was 3. Therapy was well tolerated with few grade 3/4 toxicities including minimal neurotoxicity. On intent-to-treat, the overall response rate (ORR) at end of therapy was 70% with a complete remission (CR) rate of 40% (FL: ORR 76%, CR 44%). With 50-month median follow-up, 4-year progression-free survival (PFS) was 44% with 4-year overall survival (OS) of 87% (FL: 44% and 97%, respectively). Four-year PFS for FLIPI 0-2 vs. 3-5 was 60% vs. 26% respectively (P = 0·02), with corresponding OS rates of 92% and 81% respectively (P = 0·16). Collectively, bortezomib/rituximab is a non-cytotoxic therapeutic regimen that was well tolerated and resulted in long-term survival rates approximating prior rituximab/cytotoxic chemotherapy series for untreated HTB FL.

摘要

目前缺乏针对高肿瘤负担(HTB)惰性非霍奇金淋巴瘤(iNHL)患者一线治疗的非细胞毒性选择的已发表数据。我们完成了一项针对未经治疗的 HTB iNHL 患者的多中心 II 期研究(NCT00369707),该研究包括三个周期的每周硼替佐米和利妥昔单抗诱导治疗,随后进行简短的巩固治疗。42 名患者接受了治疗,均可以进行评估;最常见的组织学类型是滤泡性淋巴瘤(FL)(n=33,79%)。患者特征包括中位年龄 62 岁(40-86 岁);38%为肿块性疾病;19%有恶性渗出液;91%为晚期疾病;FL 国际预后指数(FLIPI)评分中位数为 3。治疗耐受性良好,仅有少数 3/4 级毒性,包括轻微的神经毒性。在意向治疗人群中,治疗结束时的总缓解率(ORR)为 70%,完全缓解率(CR)为 40%(FL:ORR 为 76%,CR 为 44%)。中位随访 50 个月后,4 年无进展生存率(PFS)为 44%,4 年总生存率(OS)为 87%(FL:分别为 44%和 97%)。FLIPI 0-2 与 3-5 的 4 年 PFS 分别为 60%和 26%(P=0·02),相应的 OS 率分别为 92%和 81%(P=0·16)。总体而言,硼替佐米/利妥昔单抗是一种非细胞毒性治疗方案,耐受性良好,长期生存率与未经治疗的 HTB FL 的先前利妥昔单抗/细胞毒性化疗系列相近。

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