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首页> 外文期刊>Leukemia and lymphoma >Nodular lymphocyte predominant Hodgkin lymphoma behaves as a distinct clinical entity with good outcome: evidence from 14-year follow-up in the West of Scotland Cancer Network.
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Nodular lymphocyte predominant Hodgkin lymphoma behaves as a distinct clinical entity with good outcome: evidence from 14-year follow-up in the West of Scotland Cancer Network.

机译:结节性淋巴细胞为主的霍奇金淋巴瘤表现为具有良好预后的独特临床实体:来自苏格兰西部癌症网络14年随访的证据。

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摘要

Clinically and biologically, nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) has much more in common with germinal-center derived B-cell non-Hodgkin lymphoma (NHL) than with classical Hodgkin lymphoma (cHL). Management of NLPHL remains controversial. In a 14-year multicenter series, 69 cases were analyzed, and the median follow-up was 53 months (range 11-165.) B-symptoms were present in only 4.3% of patients, and 81.1% of patients had stage I/II disease. Treatment was with radiotherapy (53.6%), chemotherapy (21.7%), combined modality (17.4%), and observation (7.2%). In all, 10.1% of patients relapsed and 2.9% of patients developed high-grade transformation to DLBCL. All relapses and transformations were salvageable. No patient died of their disease. The 5-year relapse-free survival was 92%, transformation-free survival 98.4%, and overall survival 100%. We conclude that NLPHL behaves as a distinct clinical entity, often presenting at an early stage without risk factors. It has an excellent outcome. It may be possible, in early-stage disease, to reduce the intensity of therapy in NLPHL, to single-modality radiotherapy, without affecting OS.
机译:在临床上和生物学上,结节性淋巴细胞为主的霍奇金淋巴瘤(NLPHL)与生发中心衍生的B细胞非霍奇金淋巴瘤(NHL)相比,比经典霍奇金淋巴瘤(cHL)更多。 NLPHL的管理仍存在争议。在为期14年的多中心研究中,分析了69例病例,中位随访时间为53个月(范围11-165。)B症状仅在4.3%的患者中出现,而81.1%的患者患有I /二,疾病。治疗方法包括放疗(53.6%),化学疗法(21.7%),综合治疗(17.4%)和观察(7.2%)。总计,有10.1%的患者复发,有2.9%的患者发展为向DLBCL的高度转化。所有复发和转化都是可挽救的。没有患者死于疾病。 5年无复发生存率为92%,无转化生存率为98.4%,总生存率为100%。我们得出的结论是,NLPHL表现为独特的临床实体,通常在早期出现而没有危险因素。它有一个极好的结果。在早期疾病中,有可能在不影响OS的情况下,将NLPHL的治疗强度降低至单模放疗。

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