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骨原发性淋巴瘤:一项基于人群的2558例患者研究。

Primary lymphoma of bone: a population-based study of 2558 patients.

作者信息

Liu Chen-Xin, Xu Tian-Qi, Xu Li, Wang Pan-Pan, Cao Chun, Gao Guang-Xun, Zheng Yan-Hua

机构信息

Institute of Orthopedics, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.

Department of Hematology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.

出版信息

Ther Adv Hematol. 2020 Sep 17;11:2040620720958538. doi: 10.1177/2040620720958538. eCollection 2020.

Abstract

BACKGROUND

Primary lymphoma of bone (PLB) is an extremely rare malignancy arising in the skeletal system. There is no consensus over the best definition of PLB. Most of the published articles are single-institutional retrospective studies with a limited sample size. The rarity of PLB and discrepancies on diagnostic criteria has resulted in a vague understanding of PLB.

METHODS

We retrospectively analyzed the clinical characteristics and prognostic factors of 2558 PLB patients who were registered in the Surveillance, Epidemiology, and End Results (SEER) database from 1973 to 2016. Survival rates were calculated using the Kaplan-Meier method. The effects of various factors on survival outcomes were analyzed by using the log-rank test. Univariate and multivariate analyses were conducted by using the Cox proportional hazards model to determine independent prognostic factors.

RESULTS

The median follow-up time of all eligible patients was 58 months. There seemed no sex preponderance in PLB incidence. The most involved sites are axial skeletons. The most common histological subtype was diffuse large B-cell lymphoma. The 3-, 5-, 10-, and 20-year overall survival (OS) rates were 70.70%, 65.70%, 54.40% and 39.50%, respectively. PLB patients whose primary tumor sites were appendicular and craniofacial skeletons had a significant survival advantage [hazard ratio (HR) = 0.694, 95% confidence interval (CI) 0.552-0.872; HR = 0.729, 95% CI 0.597-0.889, respectively] over those with axial skeletons as primary tumor sites. Patients with Hodgkin lymphoma, non-Hodgkin lymphoma (NHL)-mature B-cell lymphoma, and NHL-precursor-cell lymphoblastic lymphoma also had a significant OS advantage (HR = 0.392, 95% CI 0.200-0.771; HR = 0.826, 95% CI 0.700-0.973; and HR = 0.453, 95% CI 0.223-0.923, respectively). Patients with Ann Arbor stage III-IV at diagnosis were at higher risk of death than those with stage I-II (HR = 1.348, 95% CI 1.107-1.641). Chemotherapy was an independent favorable prognostic factor (HR = 0.734, 95% CI 0.605-0.890).

CONCLUSIONS

Primary anatomic site, histology type, higher Ann Arbor stage and chemotherapy were independent prognostic factors. Chemotherapy played a pivotal role in PLB treatment.

摘要

背景

骨原发性淋巴瘤(PLB)是一种发生于骨骼系统的极为罕见的恶性肿瘤。关于PLB的最佳定义尚无共识。大多数已发表的文章是单机构回顾性研究,样本量有限。PLB的罕见性以及诊断标准的差异导致对其认识模糊。

方法

我们回顾性分析了1973年至2016年在监测、流行病学和最终结果(SEER)数据库中登记的2558例PLB患者的临床特征和预后因素。采用Kaplan-Meier法计算生存率。使用对数秩检验分析各种因素对生存结果的影响。采用Cox比例风险模型进行单因素和多因素分析,以确定独立的预后因素。

结果

所有符合条件患者的中位随访时间为58个月。PLB发病率似乎无性别优势。最常累及的部位是中轴骨骼。最常见的组织学亚型是弥漫性大B细胞淋巴瘤。3年、5年、10年和20年总生存率(OS)分别为70.70%、65.70%、54.40%和39.50%。以四肢和颅面骨骼为原发性肿瘤部位的PLB患者比以中轴骨骼为原发性肿瘤部位的患者具有显著的生存优势[风险比(HR)=0.694,95%置信区间(CI)0.552 - 0.872;HR = 0.729,95% CI 0.597 - 0.889]。霍奇金淋巴瘤、非霍奇金淋巴瘤(NHL)-成熟B细胞淋巴瘤和NHL-前体细胞淋巴母细胞淋巴瘤患者也具有显著的OS优势(HR分别为0.392,95% CI 0.200 - 0.771;HR = 0.826,95% CI 0.700 - 0.973;HR = 0.453,95% CI 0.223 - 0.923)。诊断时Ann Arbor分期为III-IV期的患者比I-II期患者死亡风险更高(HR = 1.348,95% CI 1.107 - 1.641)。化疗是一个独立的有利预后因素(HR = 0.734,95% CI 0.605 - 0.890)。

结论

原发性解剖部位、组织学类型、较高的Ann Arbor分期和化疗是独立的预后因素。化疗在PLB治疗中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b0/7502855/91803b7c9390/10.1177_2040620720958538-fig1.jpg

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