|本期目录/Table of Contents|

[1]李兆雪,杨吉龙,朱泽.新型冠状病毒感染对恶性周围神经鞘瘤复发的观察性研究[J].天津医科大学学报,2025,31(03):268-273,387.[doi:10.20135/j.issn.1006-8147.2025.03.0268]
 LI Zhaoxue,YANG Jilong,ZHU Ze.An observational study on the effect of SARS-CoV-2 infection on the recurrence of malignant peripheral nerve sheath tumors[J].Journal of Tianjin Medical University,2025,31(03):268-273,387.[doi:10.20135/j.issn.1006-8147.2025.03.0268]
点击复制

新型冠状病毒感染对恶性周围神经鞘瘤复发的观察性研究(PDF)

《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
31卷
期数:
2025年03期
页码:
268-273,387
栏目:
临床医学
出版日期:
2025-05-20

文章信息/Info

Title:
An observational study on the effect of SARS-CoV-2 infection on the recurrence of malignant peripheral nerve sheath tumors
文章编号:
1006-8147(2025)03-0268-07
作者:
李兆雪12杨吉龙3朱泽1
(1.天津医科大学基础医学院病原生物学系,天津 300070;2.天津市津南医院检验科,天津 300350;3.天津医科大学肿瘤医院骨与软组织肿瘤科,天津 300060)
Author(s):
LI Zhaoxue12YANG Jilong3ZHU Ze1
(1.Department of Pathogen Biology,School of Basic Medical Sciences,Tianjin Medical University,Tianjin 300070,China;2. Clinical Laboratory,Tianjin Jinnan Hospital,Tianjin 300350,China;3. Department of Bone and Soft Tissue Oncology,Tianjin Medical University Cancer Institute & Hospital,Tianjin 300060,China)
关键词:
恶性周围神经鞘瘤新型冠状病毒感染复发生存曲线
Keywords:
malignant peripheral nerve sheath tumorSARS-CoV-2 infectionrecurrencesurvival curve
分类号:
R739.43
DOI:
10.20135/j.issn.1006-8147.2025.03.0268
文献标志码:
A
摘要:
目的:探讨新型冠状病毒(SARS-CoV-2)感染对恶性周围神经鞘瘤(MPNST)患者的影响,为MPNST患者的个体化治疗提供科学依据。方法:收集并分析天津医科大学肿瘤医院2018年1月至2023年12月经病理确诊为MPNST的患者数据,共纳入 48 例,根据是否感染SARS-CoV-2分为感染组(19 例)与对照组(29 例),通过电话的方式对两组患者进行随访。卡方检验及Fisher确切检验用于患者生存、复发、转移等指标的对比,Kaplan-Meier法用于计算生存曲线,Log-rank检验比较不同组间生存曲线的差异,Cox回归分析检验SARS-CoV-2感染是否为MPNST患者疾病进展的独立危险因素。结果:本研究对 48 例MPNST患者进行了分析,发现肿瘤原发部位以四肢最常见,占比43.7%。组织学分级以高级别肿瘤为主,占比79.2%。肿瘤平均最大直径约为 6.3 cm。病理学上,MPNST主要表现为恶性梭形细胞肉瘤,且S-100阳性表达率77.1%。在复发与转移方面,感染组复发率(57.9%)显著高于对照组(24.1%),差异具有统计学意义(χ2=5.581,P=0.018)。然而,在总死亡、总疾病进展、单纯转移及特定部位转移等方面,两组间未观察到差异具有统计学意义(均P>0.05)。单因素分析结果显示,SARS-CoV-2感染与MPNST复发有显著相关性(χ2=5.581,P=0.018),然而,年龄、肿瘤大小、S-100表达状态、组织学分级等因素与MPNST复发无关(均P>0.05)。感染组从SARS-CoV-2检测阳性后发生疾病进展的中位时间较对照组短(11个月 vs. 15个月,P=0.047)。但多因素Cox回归分析显示,SARS-CoV-2感染并非MPNST患者疾病进展的独立危险因素(P=0.186)。结论:SARS-CoV-2感染可能增加MPNST患者的复发风险,加速疾病进展,但对总生存期没有影响。。
Abstract:
Objective:To investigate the impact of SARS-CoV-2 infection on patients with malignant peripheral nerve sheath tumor (MPNST),aiming to provide a scientific basis for individualized treatment of patients with MPNST. Methods:Data from patients with pathologically confirmed MPNST at Tianjin Medical University Cancer Institute & Hospital between January,2018 and December,2023 were collected and analyzed,with a total of 48 patients included. The patients were divided into infected group (19 patients) and control group (29 patients) based on their COVID-19 infection status. Follow-up on the conditions of patients in both groups was conducted via telephone. Chi-square test and Fisher′s exact test were used to compare survival,recurrence,metastasis,and other indicators. Kaplan-Meier method was employed to calculate survival curves,and Log-rank test was used to compare differences in survival curves between different groups. Cox regression analysis was conducted to test whether SARS-CoV-2 infection was an independent risk factor for disease progression in patients with MPNST. Results:This study analyzed 48 MPNST patients and found that the primary tumor site was most commonly located in the extremities,accounting for 43.7% of cases. The histological grading was predominantly high-grade tumors,accounting for 79.2% of the cases. The average maximum diameter of the tumors was approximately 6.3 cm. Pathologically,MPNST mainly manifests as a malignant spindle cell sarcoma,with an S-100 positive expression rate of 77.1%. In terms of recurrence and metastasis,the recurrence rate in the infected group (57.9%) was significantly higher than that in the control group (24.1%),with a statistically significant difference (χ2=5.581,P=0.018). However,no statistically significant differences were observed between the two groups in terms of overall mortality,overall disease progression,pure metastasis,and metastasis to specific sites (all P>0.05). The results of univariate analysis showed a significant correlation between SARS-CoV-2 infection and MPNST recurrence (χ2=5.581,P=0.018). However,factors such as age,tumor size,S-100 expression status,and histological grade were not significantly associated with MPNST recurrence (all P>0.05). The median time for disease progression after a positive SARS-CoV-2 test in the infected group was shorter than that in the control group (11 months vs. 15 months,P=0.047). Yet,multivariate Cox regression analysis showed that SARS-CoV-2 infection was not an independent risk factor for disease progression in patients with MPNST (P=0.186). Conclusion:SARS-CoV-2 infection may increase the risk of recurrence and accelerate disease progression in patients with MPNST,but it has no impact on overall survival.

参考文献/References:

[1] ROTHAN H A,BYRAREDDY S N. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak[J]. J Autoimmun,2020,109:102433.
[2] WANG H D,PAULSON K R, PEASE S A,et al. Estimating excess mortality due to the COVID-19 pandemic:a systematic analysis of COVID-19-related mortality,2020-21[J]. Lancet,2022,399(10334):1513-1536.
[3] XIONG N,SUN Q. How does SARS-CoV-2 infection impact on immunity,procession and treatment of pan cancers[J]. J Med Virol,2023,95(2):e28487.
[4] OGAREK N,OBOZA P,OLSZANECKA-GLINIANOWICZ M,et al. SARS-CoV-2 infection as a potential risk factor for the development of cancer[J]. Front Mol Biosci,2023,10:1260776.
[5] SARKAR S R,SINGHAVI H R,DAS A,et al. Effects of viral infections like COVID-19 on head and neck cancers:the role of neutrophil-lymphocyte counts and ratios[J]. Cureus,2024,16(6):e61733.
[6] GREGORY T A,KNIGHT S R,AAROE A E,et al. Accelerated tumor progression after COVID-19 infection in patients with glioblastoma:a retrospective case-control study[J]. Neurooncol Pract,2024, 11(4):475-483.
[7] PENG Y L,WANG Z Y,ZHONG R W,et al. Association of COVID-19 and lung cancer:short-term and long-term interactions[J].Cancers (Basel),2024 ,16(2):304.
[8] CHEN J,DAI L,BARRETT L,et al. SARS-CoV-2 proteins and anti-COVID-19 drugs induce lytic reactivation of an oncogenic virus[J]. Commun Biol,2021,4(1):682.
[9] LAMBAREY H,BLUMENTHAL M J,CHETRAM A,et al. Reactivation of Kaposi′s sarcoma-associated herpesvirus (KSHV) by SARS-CoV-2 in non-hospitalised HIV-infected patients[J]. EBio- Medicine,2024,100:104986.
[10] LI J,BAI H,QIAO H,et al. Causal effects of COVID-19 on cancer risk:a Mendelian randomization study[J]. J Med Virol,2023,95(4):e28722.
[11] WANG H,FANG N,MOZUMDER P,et al. Exploring the protective association between COVID-19 infection and laryngeal cancer:insights from a Mendelian randomization study[J]. Front Immunol,2024,15:1380982.
[12] RAGONE C,MAURIELLO A,CAVALLUZZO B,et al. Molecular mimicry of SARS-COV-2 antigens as a possible natural anti-cancer preventive immunization[J]. Front Immunol,2024,15:1398002.
[13] TROJANI M,CONTESSO G,COINDRE J M,et al. Soft-tissue sarcomas of adults;study of pathological prognostic variables and definition of a histopathological grading system[J]. Int J Cancer,1984, 33(1):37-42.
[14] 中华人民共和国国家卫生健康委员会. 新型冠状病毒感染诊疗方案(试行第十版)[J]. 中国合理用药探索,2023,20(1):1-11.
[15] TAY M Z,POH C M,R?魪NIA L,et al. The trinity of COVID-19:immunity,inflammation and intervention[J]. Nat Rev Immunol,2020, 20(6):363-374.
[16] JIANG R D,LIU M Q,CHEN Y,et al. Pathogenesis of SARS-CoV-2 in transgenic mice expressing human angiotensin-converting enzyme 2[J]. Cell,2020,182(1):50-58.
[17] HUANG C,WANG Y,LI X,et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan,China[J]. Lancet,2020,395(10223):497-506.
[18] ZHOU R,TO K K,WONG Y C,et al. Acute SARS-CoV-2 infection impairs dendritic cell and T cell responses[J]. Immunity,2020,53(4):864-877.
[19] QIN C,ZHOU L,HU Z,et al. Dysregulation of immune response in patients with Coronavirus 2019 (COVID-19) in Wuhan,China[J]. Clin Infect Dis,2020,71(15):762-768.
[20] DU PLESSIS M,FOURIE C,RIEDEMANN J,et al. Cancer and Covid-19:collectively catastrophic[J]. Cytokine Growth Factor Rev,2022,63:78-89.
[21] CHAKRABORTY C,SHARMA A R,BHATTACHARYA M,et al. A detailed overview of immune escape,antibody escape,partial vaccine escape of SARS-CoV-2 and their emerging variants with escape mutations[J]. Front Immunol,2022,13:801522.
[22] SUN D,XIE X P,ZHANG X,et al. Stem-like cells drive NF1-associated MPNST functional heterogeneity and tumor progression[J].Cell Stem Cell,2021,28(8):1397-1410.
[23] GUTMANN D H,FERNER R E,LISTERNICK R H,et al. Neurofibromatosis type 1[J]. Nat Rev Dis Primers,2017,3:17004.
[24] MIETTINEN M M,ANTONESCU C R,FLETCHER CDM,et al. Histopathologic evaluation of atypical neurofibromatous tumors and their transformation into malignant peripheral nerve sheath tumor in patients with neurofibromatosis 1-a consensus overview[J]. Hum Pa-thol,2017,67:1-10.
[25] SOMATILAKA B N,SADEK A,MCKAY R M,et al. Malignant peripheral nerve sheath tumor:models,biology,and translation[J]. Oncogene,2022,41(17):2405-2421.
[26] SUPPIAH S,MANSOURI S,MAMATJAN Y,et al. Multiplatform molecular profiling uncovers two subgroups of malignant peripheral nerve sheath tumors with distinct therapeutic vulnerabilities[J]. Nat Commun,2023,14(1):2696.
[27] KHAN S,SHAFIEI M S,LONGORIA C,et al. SARS-CoV-2 spike protein induces inflammation via TLR2-dependent activation of the NF-κB pathway[J]. Elife,2021,10:e68563.
[28] RAPTI V,TSAGANOS T,VATHIOTIS I A,et al. New insights into SARS-CoV-2 and cancer cross-talk:does a novel oncogenesis driver emerge[J]. Vaccines (Basel),2022,10(10):1607.
[29] MATTICK J S,AMARAL P P,CARNINCI P,et al. Long non-coding RNAs:definitions,functions,challenges and recommendations[J]. Nat Rev Mol Cell Biol,2023,24(6):430-447.
[30] BEHURA A,NAIK L,PATEL S,et al. Involvement of epigenetics in affecting host immunity during SARS-CoV-2 infection[J]. Biochim Biophys Acta Mol Basis Dis,2023,1869(3):166634.
[31] MA-LAUER Y,CARBAJO-LOZOYA J,HEIN M Y,et al. P53 down-regulates SARS coronavirus replication and is targeted by the SARS-unique domain and PLpro via E3 ubiquitin ligase RCHY1[J]. Proc Natl Acad Sci U S A,2016 ,113(35):E5192-201.
[32] 刘娟,曹雪涛. 2023年国内外免疫学研究重要进展[J]. 中国免疫学杂志,2024,40(1):1-10.

相似文献/References:

[1]宋紫暄,李光明,张 静,等.H3K27三甲基化蛋白可作为MPNST的重要诊断标记物[J].天津医科大学学报,2018,24(04):353.
 SONG Zi-xuan,LI Guang-ming,ZHANG Jing,et al.H3K27me3 is a highly sensitive diagnostic marker for MPNST[J].Journal of Tianjin Medical University,2018,24(03):353.
[2]孙硕遥,高雅,朱香熹,等.吉非替尼通过促进H3K27甲基化水平抑制恶性周围神经鞘瘤细胞的增殖[J].天津医科大学学报,2021,27(03):211.
 SUN Shuo-yao,GAO Ya,ZHU Xiang-xi,et al.Gefitinib inhibits the proliferation of malignant peripheral nerve sheath tumor cells by promoting H3K27 methylation levels[J].Journal of Tianjin Medical University,2021,27(03):211.
[3]高雅,赵洋,朱香熹,等.司美替尼对恶性周围神经鞘瘤细胞增殖和凋亡的影响[J].天津医科大学学报,2022,28(01):40.
 GAO Ya,ZHAO Yang,ZHU Xiang-xi,et al.The effect of selumetinib on cell proliferation and apoptosis of malignant peripheral nerve sheath tumor[J].Journal of Tianjin Medical University,2022,28(03):40.
[4]赵洋,孙亚敏,朱香熹,等.LATS2对恶性周围神经鞘瘤细胞的调控作用及分子机制探讨[J].天津医科大学学报,2023,29(02):120.
 ZHAO Yang,SUN Ya-min,ZHU Xiang-xi,et al.Regulatory effect and molecular mechanism of LATS2 on malignant peripheral nerve sheath tumor cells[J].Journal of Tianjin Medical University,2023,29(03):120.
[5]孙亚敏,朱香熹,陈毓锴,等.萝卜硫素预防Ⅰ型神经纤维瘤病恶性进展的作用机制研究[J].天津医科大学学报,2024,30(02):105.[doi:10.20135/j.issn.1006-8147.2024.02.0105]
 SUN Yamin,ZHU Xiangxi,CHEN Yukai,et al.The effect and mechanism of sulforaphane in preventing malignant progression of neurofibromatosis type Ⅰ[J].Journal of Tianjin Medical University,2024,30(03):105.[doi:10.20135/j.issn.1006-8147.2024.02.0105]

备注/Memo

备注/Memo:
基金项目: 国家自然科学基金(81672650)
作者简介: 李兆雪(1994-),女,硕士在读,研究方向:病原生物学;
通信作者:朱泽,E-mail:zhuze@tmu.edu.cn。
更新日期/Last Update: 2025-06-01