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2
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Eur J Haematol. 2025 Sep;115(3):260-265. doi: 10.1111/ejh.14443. Epub 2025 Jun 1.
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2016 US lymphoid malignancy statistics by World Health Organization subtypes.2016年按世界卫生组织亚型分类的美国淋巴系统恶性肿瘤统计数据。
CA Cancer J Clin. 2016 Nov 12;66(6):443-459. doi: 10.3322/caac.21357. Epub 2016 Sep 12.
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Large B-cell transformation in nodular lymphocyte-predominant Hodgkin lymphoma: 40-year experience from a single institution.结节性淋巴细胞为主型霍奇金淋巴瘤中的大B细胞转化:来自单一机构的40年经验
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Hodgkin's lymphoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.霍奇金淋巴瘤:ESMO 诊断、治疗及随访临床实践指南
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Advanced-stage nodular lymphocyte predominant Hodgkin lymphoma compared with classical Hodgkin lymphoma: a matched pair outcome analysis.进展期结节性淋巴细胞为主型霍奇金淋巴瘤与经典型霍奇金淋巴瘤的比较:配对结局分析。
Blood. 2014 Jun 5;123(23):3567-73. doi: 10.1182/blood-2013-12-541078. Epub 2014 Apr 8.
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Lymphocyte-predominant Hodgkin lymphoma: what is the optimal treatment?淋巴细胞为主型霍奇金淋巴瘤:最佳治疗方案是什么?
Hematology Am Soc Hematol Educ Program. 2013;2013:406-13. doi: 10.1182/asheducation-2013.1.406.
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How I treat nodular lymphocyte predominant Hodgkin lymphoma.我是如何治疗结节性淋巴细胞为主型霍奇金淋巴瘤的。
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9
Treatment outcome after low intensity chemotherapy [CVP] in children and adolescents with early stage nodular lymphocyte predominant Hodgkin's lymphoma - an Anglo-French collaborative report.儿童和青少年早期结节性淋巴细胞为主型霍奇金淋巴瘤低强度化疗 [CVP] 后的治疗结果 - 英法合作报告。
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R-CHOP方案用于晚期结节性淋巴细胞为主型霍奇金淋巴瘤的鼓舞人心的疗效

Encouraging activity for R-CHOP in advanced stage nodular lymphocyte-predominant Hodgkin lymphoma.

作者信息

Fanale Michelle A, Cheah Chan Yoon, Rich Amy, Medeiros L Jeffrey, Lai Chao-Ming, Oki Yasuhiro, Romaguera Jorge E, Fayad Luis E, Hagemeister F B, Samaniego Felipe, Rodriguez Maria A, Neelapu Sattva S, Lee Hun J, Nastoupil Loretta, Fowler Nathan H, Turturro Francesco, Westin Jason R, Wang Michael L, McLaughlin Peter, Pinnix Chelsea C, Milgrom Sarah A, Dabaja Bouthaina, Horowitz Sandra B, Younes Anas

机构信息

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

Department of Haematology, Sir Charles Gairdner Hospital, Nedlands, WA, Australia.

出版信息

Blood. 2017 Jul 27;130(4):472-477. doi: 10.1182/blood-2017-02-766121. Epub 2017 May 18.

DOI:10.1182/blood-2017-02-766121
PMID:28522441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5578726/
Abstract

Nodular lymphocyte Hodgkin lymphoma (NLPHL) is a rare disease for which the optimal therapy is unknown. We hypothesized that rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) could decrease rates of relapse and transformation. We retrospectively reviewed patients with NLPHL diagnosed between 1995 and 2015 confirmed by central pathologic review. Fifty-nine had sufficient treatment and follow-up data for analysis. We described progression-free survival (PFS), overall survival (OS), and histologic transformation according to treatment strategy and explored prognostic factors for PFS and OS. The median age at diagnosis was 41 years; 75% were male, and 61% had a typical growth pattern. Twenty-seven patients were treated with R-CHOP with an overall response rate of 100% (complete responses 89%). The median follow-up was 6.7 years, and the estimated 5- and 10-year PFS rates for patients treated with R-CHOP were 88.5% (95% confidence interval [CI], 68.4% to 96.1%) and 59.3 (95% CI, 25.3% to 89.1%), respectively. Excluding patients with histologic transformation at diagnosis, the 5-year cumulative incidence of histologic transformation was 2% (95% CI, 87% to 100%). No patient treated with R-CHOP experienced transformation. A high-risk score from the German Hodgkin Study Group was adversely prognostic for OS ( = .036), whereas male sex and splenic involvement were adversely prognostic for PFS ( = .006 and .002, respectively) but not OS. Our data support a potential role for R-CHOP in patients with NLPHL. Larger prospective trials are needed to define the optimal chemotherapy regimen.

摘要

结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)是一种罕见疾病,其最佳治疗方案尚不清楚。我们推测利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)可降低复发和转化率。我们回顾性分析了1995年至2015年间经中心病理检查确诊的NLPHL患者。59例患者有足够的治疗和随访数据用于分析。我们根据治疗策略描述了无进展生存期(PFS)、总生存期(OS)和组织学转化情况,并探讨了PFS和OS的预后因素。诊断时的中位年龄为41岁;75%为男性,61%具有典型的生长模式。27例患者接受了R-CHOP治疗,总缓解率为100%(完全缓解率89%)。中位随访时间为6.7年,接受R-CHOP治疗的患者估计5年和10年PFS率分别为88.5%(95%置信区间[CI],68.4%至96.1%)和59.3%(95%CI,25.3%至89.1%)。排除诊断时即有组织学转化的患者,组织学转化的5年累积发生率为2%(95%CI,87%至100%)。接受R-CHOP治疗的患者均未发生转化。德国霍奇金研究组的高危评分对OS有不良预后影响(P = 0.036),而男性和脾受累对PFS有不良预后影响(分别为P = 0.006和P = 0.002),但对OS无影响。我们的数据支持R-CHOP在NLPHL患者中的潜在作用。需要更大规模的前瞻性试验来确定最佳化疗方案。