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原发性骨淋巴瘤中软组织侵犯、国际预后指数和多灶性的预后意义:单机构经验。

Prognostic significance of soft tissue extension, international prognostic index, and multifocality in primary bone lymphoma: a single institutional experience.

机构信息

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijng, China.

出版信息

Br J Haematol. 2014 Jul;166(1):60-8. doi: 10.1111/bjh.12841. Epub 2014 Mar 27.

Abstract

Primary bone lymphoma (PBL) is a rare disease. The literature is inconsistent in regard to definition, stage and prognostic factors. We examined the PBL cases seen at the Moffitt Cancer Center between 1998 and 2013 using the 2013 World Health Organization criteria for bone/soft tissue tumours. Seventy PBL patients were included, of whom 53 (75.7%) patients were histologically classified as primary bone diffuse large B-cell lymphoma (PB-DLBCL). Femur was the most commonly involved site in PBLs with unifocal bone lesions, whereas PBLs with multifocal bone lesions most frequently presented with spine disease. Further analysis of the PB-DLBCL subgroup showed that these patients had 3- and 5-year progression-free survival (PFS) of 61.2% and 46.9%, respectively and 5- and 10-year overall survival (OS) of 81.1% and 74.7%, respectively. Multivariate analysis identified soft tissue extension and International Prognostic Index (IPI) score as the most important unfavourable prognostic factors for both PFS and OS. Multifocality was also highly significantly associated with a worse PFS (P = 0.002) and OS (P < 0.001), although it was not identified in multivariate analysis due to its incorporation into the IPI. The results warrant further investigation regarding whether PBL with multifocal bone lesions could be considered as a systemic and more aggressive disease rather than a conventional PBL.

摘要

原发性骨淋巴瘤(PBL)是一种罕见疾病。关于其定义、分期和预后因素,文献报道并不一致。我们使用 2013 年世界卫生组织(WHO)骨/软组织肿瘤分类标准,对 1998 年至 2013 年期间在 Moffitt 癌症中心就诊的 PBL 患者进行了研究。共纳入 70 例 PBL 患者,其中 53 例(75.7%)患者的组织学分类为原发性骨弥漫性大 B 细胞淋巴瘤(PB-DLBCL)。股骨是 PBL 最常受累的部位,表现为单灶性骨病变,而多灶性骨病变的 PBL 最常表现为脊柱疾病。对 PB-DLBCL 亚组的进一步分析显示,这些患者的 3 年和 5 年无进展生存率(PFS)分别为 61.2%和 46.9%,5 年和 10 年总生存率(OS)分别为 81.1%和 74.7%。多因素分析确定软组织侵犯和国际预后指数(IPI)评分是影响 PFS 和 OS 的最重要的不良预后因素。多发病灶也与更差的 PFS(P=0.002)和 OS(P<0.001)显著相关,尽管由于其被纳入 IPI 评分,在多因素分析中并未确定其为独立的预后因素。这些结果表明,有必要进一步研究多发病灶的 PBL 是否可被视为一种全身性、侵袭性更强的疾病,而不是传统的 PBL。

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