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Progress in Hodgkin lymphoma: a population-based study on patients diagnosed in Sweden from 1973-2009.霍奇金淋巴瘤的研究进展:基于瑞典 1973-2009 年诊断患者的人群研究。
Blood. 2012 Jan 26;119(4):990-6. doi: 10.1182/blood-2010-08-302604. Epub 2011 Dec 6.
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经典型霍奇金淋巴瘤幸存者中非霍奇金淋巴瘤的风险和结局。

Risk and outcome of non-Hodgkin lymphoma among classical Hodgkin lymphoma survivors.

机构信息

Division of Hematology and Oncology, Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina.

出版信息

Cancer. 2013 Sep 15;119(18):3385-92. doi: 10.1002/cncr.28194. Epub 2013 Jun 24.

DOI:10.1002/cncr.28194
PMID:23797978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3862840/
Abstract

BACKGROUND

Survivors of classical Hodgkin lymphoma (cHL) are at an increased risk of developing secondary non-Hodgkin lymphomas (sNHLs). To the authors' knowledge, the outcome of patients with sNHL compared with their de novo counterparts (dnNHL) is unknown.

METHODS

Data from 26,826 cases of HL from the Surveillance, Epidemiology, and End Results (SEER) program that were diagnosed between 1992 and 2009 were used to obtain the risk of further development of different subtypes of sNHL. The survival of patients with sNHL was compared with that of matched patients with dnNHL.

RESULTS

The estimated cumulative incidence of sNHL was 2.50% (95% confidence interval [95% CI], 2.10-2.89) at 15 years from the diagnosis of cHL. The standardized incidence ratio was 10.5 (95% CI, 8.9-12.4) for aggressive B-cell NHL, 4.0 (95% CI, 3.1-5.1) for indolent B-cell NHL, and 14.6 (95% CI, 10.3-20.1) for T-cell NHL. Patients with indolent B-cell sNHL had a worse overall survival compared with their dnNHL counterparts (hazards ratio [HR] of death, 2.7; 95% CI, 1.3-5.7). Survival was not significantly different between patients with sNHL and those with dnNHL with regard to aggressive B-cell NHL (HR, 1.3; 95% CI, 0.6-2.7) or T-cell NHL (HR, 0.8; 95% CI, 0.3-1.8).

CONCLUSIONS

The risk of developing sNHL after cHL is substantial. Although patients with indolent B-cell sNHL have inferior survival, patients with aggressive B-cell sNHL and T-cell sNHL have survival comparable to that of their de novo counterparts.

摘要

背景

经典霍奇金淋巴瘤(cHL)幸存者发生继发性非霍奇金淋巴瘤(sNHL)的风险增加。据作者所知,sNHL 患者的预后与初发非霍奇金淋巴瘤(dnNHL)患者的预后尚不清楚。

方法

利用 1992 年至 2009 年间监测、流行病学和最终结果(SEER)计划中诊断的 26826 例 HL 病例的数据,得出不同亚型 sNHL 进一步发展的风险。比较 sNHL 患者与匹配的 dnNHL 患者的生存情况。

结果

从 cHL 诊断起 15 年时,sNHL 的估计累积发病率为 2.50%(95%置信区间[95%CI],2.10-2.89)。侵袭性 B 细胞 NHL 的标准化发病比为 10.5(95%CI,8.9-12.4),惰性 B 细胞 NHL 为 4.0(95%CI,3.1-5.1),T 细胞 NHL 为 14.6(95%CI,10.3-20.1)。惰性 B 细胞 sNHL 患者的总生存情况较其 dnNHL 患者差(死亡风险比[HR],2.7;95%CI,1.3-5.7)。侵袭性 B 细胞 NHL(HR,1.3;95%CI,0.6-2.7)或 T 细胞 NHL(HR,0.8;95%CI,0.3-1.8)患者的生存情况与 dnNHL 患者无显著差异。

结论

cHL 后发生 sNHL 的风险很大。虽然惰性 B 细胞 sNHL 患者的生存情况较差,但侵袭性 B 细胞 sNHL 和 T 细胞 sNHL 患者的生存情况与初发非霍奇金淋巴瘤患者相当。