Survival analysis of malignant peripheral nerve sheath tumor: Experience of a tertiary center in Taiwan.

IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Journal of the Chinese Medical Association Pub Date : 2023-06-01 DOI:10.1097/JCMA.0000000000000930
Yu-Wei Chang, Wen-Chieh Liao
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Abstract

Background: This study aimed to analyze the demographic characteristics and prognostic factors of malignant peripheral nerve sheath tumor (MPNST) in a Taiwanese population. Single-center treatment outcomes were also presented.

Methods: This retrospective cohort study analyzed the medical records of 54 patients with pathological diagnoses of MPNSTs from 2005 to 2021 at a single institution. The primary endpoint was the 5-year overall survival rate of MPNST, and the secondary endpoint was recurrence-free 5-year survival. Variables including patient characteristics, metastasis status at initial diagnosis, and surgical outcomes were analyzed with competing risk analysis.

Results: Among all 41 eligible patients diagnosed with MPNST, female predominance was noted, and the median age at diagnosis was 44 years. The most common site of lesion was found at the trunk (46.34%), and eight patients were diagnosed with notable metastasis. Twelve patients were diagnosed with type 1 neurofibromatosis (NF1). The 5-year overall survival rate was 36.84% and the 5-year recurrence-free survival was 28.95%. Metastasis diagnosed at presentation, large lesion sizes, and recurrence were identified as significant poor prognostic factors of survival. Metastasis diagnosed at presentation was identified as the only significant risk factor of recurrence.

Conclusion: In our series, metastasis diagnosed at presentation, large lesion sizes, and recurrence were identified as significant poor prognostic factors of survival. Metastasis was also identified as the only significant risk factor of recurrence. NF1-associated MPNSTs presented with significantly larger tumor sizes and additional treatment postoperatively did not significantly improve survival. The limitations of this study include its retrospective nature and sample size.

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恶性周围神经鞘肿瘤的生存分析:台湾某三级中心的经验。
背景:本研究旨在分析台湾人群恶性周围神经鞘肿瘤(MPNST)的人口学特征及预后因素。还介绍了单中心治疗的结果。方法:本回顾性队列研究分析了同一医院2005年至2021年病理诊断为MPNSTs的54例患者的病历。主要终点是MPNST的5年总生存率,次要终点是无复发的5年生存率。变量包括患者特征、初始诊断时的转移状态和手术结果,并采用竞争风险分析进行分析。结果:41例符合条件的MPNST患者中,女性居多,诊断时的中位年龄为44岁。病变部位以躯干居多(46.34%),8例患者有明显转移。12例患者诊断为1型神经纤维瘤病(NF1)。5年总生存率为36.84%,5年无复发生存率为28.95%。在表现时诊断为转移,病变大小大,复发被认为是生存不良的重要预后因素。在发病时诊断出的转移被确定为复发的唯一重要危险因素。结论:在我们的研究中,在出现时诊断出的转移、大的病变大小和复发被认为是生存的重要不良预后因素。转移也被确定为复发的唯一重要危险因素。nf1相关的mpnst表现出明显较大的肿瘤大小,术后额外治疗并没有显著提高生存率。本研究的局限性包括其回顾性性质和样本量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of the Chinese Medical Association
Journal of the Chinese Medical Association MEDICINE, GENERAL & INTERNAL-
CiteScore
6.20
自引率
13.30%
发文量
320
审稿时长
15.5 weeks
期刊介绍: Journal of the Chinese Medical Association, previously known as the Chinese Medical Journal (Taipei), has a long history of publishing scientific papers and has continuously made substantial contribution in the understanding and progress of a broad range of biomedical sciences. It is published monthly by Wolters Kluwer Health and indexed in Science Citation Index Expanded (SCIE), MEDLINE®, Index Medicus, EMBASE, CAB Abstracts, Sociedad Iberoamericana de Informacion Cientifica (SIIC) Data Bases, ScienceDirect, Scopus and Global Health. JCMA is the official and open access journal of the Chinese Medical Association, Taipei, Taiwan, Republic of China and is an international forum for scholarly reports in medicine, surgery, dentistry and basic research in biomedical science. As a vehicle of communication and education among physicians and scientists, the journal is open to the use of diverse methodological approaches. Reports of professional practice will need to demonstrate academic robustness and scientific rigor. Outstanding scholars are invited to give their update reviews on the perspectives of the evidence-based science in the related research field. Article types accepted include review articles, original articles, case reports, brief communications and letters to the editor
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