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初诊ⅠA 期结节性淋巴细胞为主型霍奇金淋巴瘤患者接受利妥昔单抗的Ⅱ期研究:德国霍奇金研究组报告。

Phase 2 study of rituximab in newly diagnosed stage IA nodular lymphocyte-predominant Hodgkin lymphoma: a report from the German Hodgkin Study Group.

机构信息

First Department of Internal Medicine, University Hospital of Cologne, Cologne, Germany.

出版信息

Blood. 2011 Oct 20;118(16):4363-5. doi: 10.1182/blood-2011-06-361055. Epub 2011 Aug 9.

Abstract

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) accounts for ∼ 5% of Hodgkin lymphoma cases. The disease is characterized by a strong CD20 expression on the malignant cells and a more indolent clinical course compared with classic HL. Anti-CD20 antibody treatment has shown clinical activity in relapsed NLPHL. In this phase 2 trial, we investigated rituximab in newly diagnosed stage IA NLPHL patients. Four weekly applications at 375 mg/m(2) were given. Among the 28 evaluable patients, overall response rate was 100%, 24 patients (85.7%) achieved complete remission, and 4 (14.3%) achieved partial remission. At a median follow-up of 43 months, overall survival was 100%; progression-free survival at 12, 24, and 36 months was 96.4%, 85.3%, and 81.4%, respectively. No grade 3 or 4 toxicity was observed. Although treatment results with rituximab appear inferior compared with radiotherapy and combined-modality approaches in early-stage patients, investigation of anti-CD20 antibody-based combinations in NLPHL is warranted. This study was registered at www.clinicaltrials.gov as #NCT00346684.

摘要

结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)约占霍奇金淋巴瘤病例的 5%。与经典 HL 相比,该病的特征是恶性细胞上强烈表达 CD20,且临床病程更为惰性。抗 CD20 抗体治疗在复发的 NLPHL 中显示出临床活性。在这项 2 期试验中,我们研究了利妥昔单抗在新诊断的 IA 期 NLPHL 患者中的应用。每周应用 4 次,剂量为 375mg/m2。在 28 例可评估的患者中,总缓解率为 100%,24 例(85.7%)达到完全缓解,4 例(14.3%)达到部分缓解。在中位随访 43 个月时,总生存率为 100%;12、24 和 36 个月时无进展生存率分别为 96.4%、85.3%和 81.4%。未观察到 3 或 4 级毒性。尽管利妥昔单抗的治疗结果与早期患者的放疗和联合治疗方法相比似乎较差,但有必要在 NLPHL 中研究抗 CD20 抗体联合治疗。该研究在 www.clinicaltrials.gov 上注册,编号为 #NCT00346684。

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