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复发或难治性结节性淋巴细胞为主型霍奇金淋巴瘤的结局:一项北美分析。

Outcome of relapsed and refractory nodular lymphocyte-predominant Hodgkin lymphoma: a North American analysis.

机构信息

Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

BC Cancer Centre for Lymphoid Cancer and Department of Medical Oncology, BC Cancer, Vancouver, BC, Canada.

出版信息

Br J Haematol. 2021 Feb;192(3):560-567. doi: 10.1111/bjh.17281.

DOI:10.1111/bjh.17281
PMID:33517581
Abstract

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a rare entity, with limited data on the outcome in the relapsed/refractory setting. We evaluated the outcome of all patients diagnosed between 04/1979 and 01/2019 with relapsed or progressive NLPHL after initial active therapy at two institutions, refractory disease being defined as lack of response to treatment and/or relapse within three months of treatment. NLPHL patients with histological evidence of transformation at time of first relapse or progression were excluded. In total, 69 patients with recurrent NLPHL were included in the study. After a median follow-up after initial diagnosis of 14 years (range, 0·5-46 years), median progression-free survival after front-line treatment (PFS-1) was four years. Second-line therapy included chemotherapy in 28 (41%) patients, biological therapy (rituximab, lenalidomide or brentuximab vedotin) in 14 (20%), high-dose chemotherapy followed by autologous stem cell transplant in 14 (20%) and radiation therapy (RT) alone in 10 (15%). The five-year PFS after second-line therapy (PFS-2) was 68% [95% confidence interval (CI), 54-79%] but the five-year overall survival (OS) after second-line therapy (OS-2) remained excellent, at 94% (95% CI, 85-99%). Due to excellent outcome in case of recurrence, studies aimed at characterizing its biology to guide therapy de-escalation are needed.

摘要

结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)较为罕见,复发/难治性患者的结局数据有限。我们评估了两家机构在初始积极治疗后复发或进展的 NLPHL 患者的结局,复发难治性疾病定义为治疗无反应和/或治疗后 3 个月内复发。在首次复发或进展时具有组织学转化证据的 NLPHL 患者被排除在外。共有 69 例复发性 NLPHL 患者纳入研究。在初始诊断后的中位随访 14 年后(范围为 0.5-46 年),一线治疗后的无进展生存(PFS-1)的中位数为 4 年。二线治疗包括 28 例(41%)患者化疗、14 例(20%)患者接受生物治疗(利妥昔单抗、来那度胺或 Brentuximab vedotin)、14 例(20%)患者接受大剂量化疗后自体干细胞移植和 10 例(15%)患者单纯接受放疗。二线治疗后的 5 年 PFS(PFS-2)为 68%(95%CI,54-79%),但二线治疗后的 5 年总生存(OS)仍然极好,为 94%(95%CI,85-99%)。由于复发后的结局极好,因此需要开展研究以明确其生物学特征,从而指导治疗降阶梯。

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