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脾切除术对伴有脾脏受累的淋巴瘤预后的影响。

Impact of splenectomy on prognosis in lymphoma with splenic involvement.

作者信息

Li Li, Xiong Mengqi, Wang Lulu, Zhu Lixia, Zhao Kui, Wang Lijun, He Jingsong, Ye Xiujin

机构信息

Department of Hematology, Bone Marrow Transplantation Center, the First Affiliated Hospital, College of Medicine, Zhejiang University School of Medicine, 79# Qingchun Road, Hangzhou, 310003, China.

Program in Clinical Medicine, School of Medicine of Zhejiang University, Zhejiang Province, Hangzhou, China.

出版信息

Eur J Med Res. 2025 Mar 28;30(1):213. doi: 10.1186/s40001-025-02465-y.

DOI:10.1186/s40001-025-02465-y
PMID:40149024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11951545/
Abstract

BACKGROUND

Lymphoma presenting splenic invasion as the primary manifestation poses unique diagnostic and therapeutic challenges. This study aims to systematically analyze the clinical features, prognostic factors, and outcomes of patients with splenic involvement as the initial presentation of lymphoma.

METHODS

A retrospective analysis was conducted on lymphoma patients diagnosed with splenic involvement confirmed by histopathological examination at our hospital from March 2011 to February 2023. A total of 113 patients were included based on predefined inclusion and exclusion criteria. The collected data encompassed clinical presentations, diagnostic methods, histopathological features, treatment regimens, and outcomes. Kaplan-Meier survival analysis was performed to generate survival curves for overall survival (OS) and progression-free survival (PFS), with statistical significance assessed using the log-rank test. Additionally, univariate and multivariate analyses utilizing Cox regression analyses were conducted to identify potential prognostic factors.

RESULTS

According to the pathological results, there were 6 types of lymphoma: indolent lymphoma (n = 23.18 of splenic marginal zone lymphoma (SMZL), 4 of follicular lymphoma (FL), 1 of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). Aggressive lymphoma (n = 90.74 of diffuse large B cell lymphoma (DLBCL), 10 of NK/T cell lymphoma, 4 of mantle cell lymphoma (MCL), 1 of T lymphoblastic lymphoma, 1 of EBV-positive T cell lymphoma). Diagnosis was confirmed by hollow needle biopsy in 42 patients and through diagnostic splenectomy in 71 patients. 12 patients underwent splenectomy alone while 59 received chemotherapy following splenectomy. The median follow-up time was 37.53 months (range 0 to 162.33 months). The overall 5 year survival (OS) rate for the entire cohort was 62.39% and the 5 year progression-free survival (PFS) rate was 53.98%. Among those who underwent splenectomy, the 5 year OS rate and 5 year PFS rate were 68.06 and 62.50%, which were superior to 52.44 and 37.80% for non-splenectomy patients (P = 0.009 and P < 0.001, respectively). These differences were also observed in the aggressive lymphoma subgroup (n = 90), the 5 year OS rate and 5 year PFS rate were 62.96 and 57.41%, which were also superior to 48.61 and 37.50% for non-splenectomy patients (P = 0.042 and P = 0.017, respectively). In the whole group (n = 110), multivariate model shows prolonged APTT (P = 0.024), virous treatments (P = 0.016) and elevated ferritin (P = 0.017) were independent predicted OS parameters. In aggressive lymphoma subtype (n = 87), treatment (P = 0.021) and prolonged APTT (P = 0.016) emerged as independent risk factors. In indolent lymphomas, no significant differences were found.

CONCLUSION

In this group of lymphoma patients presenting with splenic invasion as the first manifestation, the pathological type was almost aggressive lymphoma, with DLBCL being the main subtype. Common clinical symptoms include elevated ferritin, prolonged APTT and high LDH levels. This study suggests that splenectomy should be considered for these patients when their overall condition allows for safe intervention. Splenectomy combined with chemotherapy can significantly improve the survival time of patients.

摘要

背景

以脾脏侵犯为主要表现的淋巴瘤带来了独特的诊断和治疗挑战。本研究旨在系统分析以脾脏受累为淋巴瘤初始表现的患者的临床特征、预后因素及结局。

方法

对2011年3月至2023年2月在我院经组织病理学检查确诊为脾脏受累的淋巴瘤患者进行回顾性分析。根据预先设定的纳入和排除标准,共纳入113例患者。收集的数据包括临床表现、诊断方法、组织病理学特征、治疗方案及结局。采用Kaplan-Meier生存分析生成总生存(OS)和无进展生存(PFS)曲线,使用对数秩检验评估统计学意义。此外,利用Cox回归分析进行单因素和多因素分析以确定潜在的预后因素。

结果

根据病理结果,有6种淋巴瘤类型:惰性淋巴瘤(n = 23,其中脾边缘区淋巴瘤(SMZL)18例,滤泡性淋巴瘤(FL)4例,慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)1例)。侵袭性淋巴瘤(n = 90,其中弥漫性大B细胞淋巴瘤(DLBCL)74例,NK/T细胞淋巴瘤10例,套细胞淋巴瘤(MCL)4例,T淋巴母细胞淋巴瘤1例,EBV阳性T细胞淋巴瘤1例)。42例患者通过空心针活检确诊,71例患者通过诊断性脾切除术确诊。12例患者仅接受脾切除术,59例患者在脾切除术后接受化疗。中位随访时间为37.53个月(范围0至162.33个月)。整个队列的5年总生存(OS)率为62.39%,5年无进展生存(PFS)率为53.98%。在接受脾切除术的患者中,5年OS率和5年PFS率分别为68.06%和62.50%,优于未接受脾切除术患者的52.44%和37.80%(P分别为0.009和P < 0.001)。在侵袭性淋巴瘤亚组(n = 90)中也观察到了这些差异,5年OS率和5年PFS率分别为62.96%和57.41%,也优于未接受脾切除术患者的48.61%和37.50%(P分别为0.042和P = 0.017)。在整个组(n = 110)中,多因素模型显示活化部分凝血活酶时间(APTT)延长(P = 0.024)、病毒治疗(P = 0.016)和铁蛋白升高(P = 0.017)是独立的总生存预测参数。在侵袭性淋巴瘤亚型(n = 87)中,治疗(P = 0.021)和APTT延长(P = 0.016)是独立的危险因素。在惰性淋巴瘤中,未发现显著差异。

结论

在这组以脾脏侵犯为首发表现的淋巴瘤患者中,病理类型多为侵袭性淋巴瘤,其中DLBCL是主要亚型。常见临床症状包括铁蛋白升高、APTT延长和乳酸脱氢酶(LDH)水平升高。本研究表明,对于这些患者,在其整体状况允许安全干预时应考虑行脾切除术。脾切除术联合化疗可显著提高患者的生存时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/d2c575049af5/40001_2025_2465_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/e3066b9457d0/40001_2025_2465_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/26c8ca955f2e/40001_2025_2465_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/d2c575049af5/40001_2025_2465_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/e3066b9457d0/40001_2025_2465_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/26c8ca955f2e/40001_2025_2465_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fa/11951545/d2c575049af5/40001_2025_2465_Fig3_HTML.jpg

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本文引用的文献

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A practical approach to the modern diagnosis and classification of T- and NK-cell lymphomas.一种实用的方法,用于现代 T 细胞和 NK 细胞淋巴瘤的诊断和分类。
Blood. 2024 Oct 31;144(18):1855-1872. doi: 10.1182/blood.2023021786.
2
The epidemiological patterns of non-Hodgkin lymphoma: global estimates of disease burden, risk factors, and temporal trends.非霍奇金淋巴瘤的流行病学模式:疾病负担、风险因素及时间趋势的全球估计
Front Oncol. 2023 Jun 2;13:1059914. doi: 10.3389/fonc.2023.1059914. eCollection 2023.
3
Incidence, mortality, risk factors, and trends for Hodgkin lymphoma: a global data analysis.
霍奇金淋巴瘤的发病率、死亡率、危险因素和趋势:全球数据分析。
J Hematol Oncol. 2022 May 11;15(1):57. doi: 10.1186/s13045-022-01281-9.
4
SPARC-positive macrophages are the superior prognostic factor in the microenvironment of diffuse large B-cell lymphoma and independent of MYC rearrangement and double-/triple-hit status.SPARC 阳性巨噬细胞是弥漫性大 B 细胞淋巴瘤微环境中具有更好预后的预测因子,且独立于 MYC 重排和双/三打击状态。
Ann Oncol. 2021 Nov;32(11):1400-1409. doi: 10.1016/j.annonc.2021.08.1991. Epub 2021 Aug 24.
5
Multiomic analysis of cytokines in immuno-oncology.免疫肿瘤学中细胞因子的多组学分析。
Expert Rev Proteomics. 2020 Sep;17(9):663-674. doi: 10.1080/14789450.2020.1845654. Epub 2020 Nov 23.
6
Plasma soluble PD-L1 and STAT3 predict the prognosis in diffuse large B cell lymphoma patients.血浆可溶性程序性死亡配体1和信号转导及转录激活因子3可预测弥漫性大B细胞淋巴瘤患者的预后。
J Cancer. 2020 Oct 17;11(23):7001-7008. doi: 10.7150/jca.47816. eCollection 2020.
7
Aggressive B-cell lymphomas with a primary bone marrow presentation.原发性骨髓内表现的侵袭性 B 细胞淋巴瘤。
Histopathology. 2020 Sep;77(3):369-379. doi: 10.1111/his.14124. Epub 2020 Jul 14.
8
Stage I Non-Hodgkin Lymphoma: difference in survival outcome by primary extranodal site of involvement.I期非霍奇金淋巴瘤:根据原发性结外受累部位的生存结果差异。
Br J Haematol. 2019 Apr;185(2):334-338. doi: 10.1111/bjh.15444. Epub 2018 Jul 5.
9
Clinicopathological and genomic analysis of double-hit follicular lymphoma: comparison with high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements.双打击滤泡淋巴瘤的临床病理和基因组分析:与伴有 MYC 和 BCL2 及/或 BCL6 重排的高级别 B 细胞淋巴瘤的比较。
Mod Pathol. 2018 Feb;31(2):313-326. doi: 10.1038/modpathol.2017.134. Epub 2017 Oct 6.
10
Minimal Treatment of Low-Risk, Pediatric Lymphocyte-Predominant Hodgkin Lymphoma: A Report From the Children's Oncology Group.儿童肿瘤协作组关于低风险、儿童淋巴细胞为主型霍奇金淋巴瘤的最小化治疗报告
J Clin Oncol. 2016 Jul 10;34(20):2372-9. doi: 10.1200/JCO.2015.65.3469. Epub 2016 May 16.