Risk and outcome of non‐Hodgkin lymphoma among classical Hodgkin lymphoma survivors

Publisher: John Wiley & Sons Inc

E-ISSN: 1097-0142|119|18|3385-3392

ISSN: 0008-543x

Source: CANCER, Vol.119, Iss.18, 2013-09, pp. : 3385-3392

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

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Abstract

BACKGROUNDSurvivors 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.METHODSData 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.RESULTSThe 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).CONCLUSIONSThe 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. Cancer 2013;119:3385–92. © 2013 American Cancer Society.