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结节性淋巴细胞为主型霍奇金淋巴瘤向侵袭性淋巴瘤的转化。

Transformation to aggressive lymphoma in nodular lymphocyte-predominant Hodgkin's lymphoma.

机构信息

MSc, British Columbia Cancer Agency, 600 West 10th Ave, Vancouver, British Columbia, V5Z 4E6.

出版信息

J Clin Oncol. 2010 Feb 10;28(5):793-9. doi: 10.1200/JCO.2009.24.9516. Epub 2010 Jan 4.

Abstract

PURPOSE Prior observations suggest a higher risk of transformation of nodular lymphocyte-predominant Hodgkin's lymphoma (NLPHL) to aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL), than in classical Hodgkin's lymphoma. We evaluated the frequency of transformation in all patients diagnosed with NLPHL at the British Columbia Cancer Agency with long-term follow-up. PATIENTS AND METHODS The Lymphoid Cancer Database of the British Columbia Cancer Agency was searched to identify all patients diagnosed with NLPHL between 1965 and 2006. After pathologic review, 95 patients with NLPHL were confirmed. Results Patients with NLPHL had the following characteristics at diagnosis: median age of 37 years, 73% male, and 68% stage I or II disease. With a median follow-up time for living patients of 6.5 years (range, 2.5 to 33 years), 13 patients (14%) experienced transformation to aggressive lymphoma (median time to transformation, 8.1 years; range, 0.35 to 20.3 years). The actuarial risk of transformation to aggressive lymphoma was 7% and 30% at 10 and 20 years, respectively. Transformation was more likely in patients with initial splenic involvement (P = .006) at the time of diagnosis of NLPHL. The 10-year progression-free and overall survival rates in patients with transformed lymphoma were 52% and 62%, respectively. CONCLUSION The risk of transformation in patients with NLPHL to DLBCL is substantial and underappreciated. Because transformation can occur years after the primary diagnosis of NLPHL, long-term follow-up of these individuals is necessary to accurately estimate the risk of development of secondary DLBCL.

摘要

目的

先前的观察结果表明,结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)转化为侵袭性淋巴瘤的风险高于经典霍奇金淋巴瘤,最常见的是弥漫性大 B 细胞淋巴瘤(DLBCL)。我们评估了在不列颠哥伦比亚癌症署(British Columbia Cancer Agency)被诊断为 NLPHL 并进行长期随访的所有患者的转化频率。

患者和方法

在不列颠哥伦比亚癌症署的淋巴瘤数据库中搜索了 1965 年至 2006 年间被诊断为 NLPHL 的所有患者。经过病理复查,共确诊了 95 例 NLPHL 患者。

结果

NLPHL 患者的诊断时特征如下:中位年龄 37 岁,男性占 73%,68%为 I 期或 II 期疾病。对于生存患者的中位随访时间为 6.5 年(范围为 2.5 至 33 年),13 例(14%)发生侵袭性淋巴瘤转化(中位转化时间为 8.1 年,范围为 0.35 至 20.3 年)。侵袭性淋巴瘤转化的累积风险分别为 10 年时 7%和 20 年时 30%。NLPHL 诊断时初始脾脏受累(P=0.006)的患者更有可能发生转化。转化为 DLBCL 的患者 10 年无进展生存率和总生存率分别为 52%和 62%。

结论

NLPHL 患者转化为 DLBCL 的风险相当大,但却被低估了。由于转化可能发生在 NLPHL 首次诊断后的多年,因此需要对这些患者进行长期随访,以准确估计发展为继发性 DLBCL 的风险。

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