首页> 外文期刊>British Journal of Haematology >Prognostic significance of soft tissue extension, International Prognostic Index, and multifocality in primary bone lymphoma: A single institutional experience
【24h】

Prognostic significance of soft tissue extension, International Prognostic Index, and multifocality in primary bone lymphoma: A single institutional experience

机译:软组织扩展,国际预后指数和原发性骨淋巴瘤多灶性的预后意义:单一机构经验

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:原发性骨淋巴瘤(PBL)是一种罕见的疾病。关于定义,阶段和预后因素,文献不一致。我们使用2013年世界卫生组织的骨/软组织肿瘤标准,对1998年至2013年在莫菲特癌症中心(Moffitt Cancer Center)所见的PBL病例进行了检查。包括70例PBL患者,其中53例(75·7%)患者按组织学分类为原发性骨弥漫性大B细胞淋巴瘤(PB-DLBCL)。在具有单灶性骨病变的PBL中,股骨是最常见的部位,而具有多灶性骨病变的PBL最常见于脊柱疾病。 PB-DLBCL亚组的进一步分析表明,这些患者的3年和5年无进展生存期(PFS)分别为61·2%和46·9%,以及5年和10年总生存期(OS)分别为81·1%和74·7%。多变量分析确定软组织扩张和国际预后指数(IPI)评分是PFS和OS的最重要的不利预后因素。多焦点还与较差的PFS(P = 0·002)和OS(P <0·001)高度相关,尽管由于将其纳入IPI而无法在多变量分析中进行识别。该结果值得进一步研究,即是否可以将具有多灶性骨病变的PBL视为一种全身性,更具侵略性的疾病,而不是传统的PBL。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号