• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Biology and Management of Undifferentiated Pleomorphic Sarcoma, Myxofibrosarcoma, and Malignant Peripheral Nerve Sheath Tumors: State of the Art and Perspectives.未分化多形性肉瘤、黏液纤维肉瘤和恶性外周神经鞘瘤的生物学特性和治疗管理:现状与展望。
J Clin Oncol. 2018 Jan 10;36(2):160-167. doi: 10.1200/JCO.2017.75.3467. Epub 2017 Dec 8.
2
Diagnosis, classification, and management of soft tissue sarcomas.软组织肉瘤的诊断、分类及管理
Cancer Control. 2005 Jan-Feb;12(1):5-21. doi: 10.1177/107327480501200102.
3
Soft tissue sarcomas.软组织肉瘤
Cancer Treat Res. 2014;162:203-23. doi: 10.1007/978-3-319-07323-1_10.
4
Pleomorphic Sarcomas: The State of the Art.多形性肉瘤:最新进展
Surg Pathol Clin. 2019 Mar;12(1):63-105. doi: 10.1016/j.path.2018.10.004. Epub 2018 Dec 17.
5
Diagnosis and management of pleomorphic sarcomas (so-called "MFH") in adults.成人多形性肉瘤(所谓的“恶性纤维组织细胞瘤”)的诊断与管理。
J Surg Oncol. 2008 Mar 15;97(4):330-9. doi: 10.1002/jso.20972.
6
The rare primary bone sarcomas: imaging-pathological correlation.罕见的原发性骨肉瘤:影像学-病理学相关性。
Skeletal Radiol. 2021 Aug;50(8):1491-1511. doi: 10.1007/s00256-020-03692-6. Epub 2021 Jan 7.
7
Assessment of The Utility of The Sarcoma DNA Methylation Classifier In Surgical Pathology.肉瘤 DNA 甲基化分类器在外科病理学中的效用评估。
Am J Surg Pathol. 2024 Jan 1;48(1):112-122. doi: 10.1097/PAS.0000000000002138. Epub 2023 Nov 3.
8
Systematic screening identifies a 2-gene signature as a high-potential prognostic marker of undifferentiated pleomorphic sarcoma/myxofibrosarcoma.系统筛查确定了 2 个基因标志物作为未分化多形性肉瘤/黏液纤维肉瘤的高潜力预后标志物。
J Cell Mol Med. 2020 Jan;24(1):1010-1021. doi: 10.1111/jcmm.14814. Epub 2019 Nov 19.
9
[Malignant fibrous histiocytoma: pleomorphic sarcoma NOS or pleomorphic fibrosarcoma].[恶性纤维组织细胞瘤:未特指的多形性肉瘤或多形性纤维肉瘤]
Pathologe. 2005 Mar;26(2):127-33. doi: 10.1007/s00292-005-0747-4.
10
Management of adult soft-tissue sarcomas of the extremities.成人四肢软组织肉瘤的管理
Surg Annu. 1979;11:363-402.

引用本文的文献

1
Immunotherapy in the Treatment of Undifferentiated Pleomorphic Sarcoma and Myxofibrosarcoma.免疫疗法在未分化多形性肉瘤和黏液纤维肉瘤治疗中的应用
Curr Treat Options Oncol. 2025 Sep 1. doi: 10.1007/s11864-025-01349-x.
2
Cancer‑associated fibroblasts in human malignancies, with a particular emphasis on sarcomas (Review).人类恶性肿瘤中的癌症相关成纤维细胞,尤其侧重于肉瘤(综述)
Int J Oncol. 2025 Oct;67(4). doi: 10.3892/ijo.2025.5785. Epub 2025 Aug 8.
3
Budd-Chiari syndrome from pleomorphic sarcoma compressing the inferior vena cava: A case report.多形性肉瘤压迫下腔静脉导致布加综合征:一例报告
Radiol Case Rep. 2025 Jul 26;20(10):5161-5164. doi: 10.1016/j.radcr.2025.06.081. eCollection 2025 Oct.
4
Cutaneous Mass with Indurated Erythema in the Right Popliteal Fossa: A Quiz.右侧腘窝伴有硬结性红斑的皮肤肿物:一则病例问答
Acta Derm Venereol. 2025 Jul 11;105:adv43722. doi: 10.2340/actadv.v105.43722.
5
[Gastric Undifferentiated Pleomorphic Sarcoma Presenting as a Rapidly Growing Subepithelial Tumor].[表现为快速生长的上皮下肿瘤的胃未分化多形性肉瘤]
Korean J Helicobacter Up Gastrointest Res. 2024 Sep;24(3):276-280. doi: 10.7704/kjhugr.2024.0033. Epub 2024 Sep 9.
6
Retroperitoneal Sarcoma (RPS): A Systematic Review.腹膜后肉瘤(RPS):一项系统评价
Curr Oncol Rep. 2025 Jun 4. doi: 10.1007/s11912-025-01690-2.
7
A Rare Intruder of the Liver: A Case of Undifferentiated Pleomorphic Sarcoma.肝脏的罕见入侵者:一例未分化多形性肉瘤
Cureus. 2025 Mar 10;17(3):e80333. doi: 10.7759/cureus.80333. eCollection 2025 Mar.
8
Machine Learning-based Identification of Prognostic Factors for Surgical Management in Patients With NOS Sarcoma.基于机器学习识别非特指型肉瘤患者手术治疗的预后因素
Plast Reconstr Surg Glob Open. 2025 Apr 2;13(4):e6653. doi: 10.1097/GOX.0000000000006653. eCollection 2025 Apr.
9
Emerging mechanism and therapeutic potential of neurofibromatosis type 1-related nerve system tumor: Advancing insights into tumor development.1型神经纤维瘤病相关神经系统肿瘤的新机制及治疗潜力:对肿瘤发展的深入洞察
Neurooncol Adv. 2025 Feb 16;7(1):vdaf040. doi: 10.1093/noajnl/vdaf040. eCollection 2025 Jan-Dec.
10
The Role of Yes-Associated Protein in Inflammatory Diseases and Cancer.Yes相关蛋白在炎症性疾病和癌症中的作用。
MedComm (2020). 2025 Mar 10;6(3):e70128. doi: 10.1002/mco2.70128. eCollection 2025 Mar.

本文引用的文献

1
Neurofibromatosis Type 1-Associated MPNST State of the Science: Outlining a Research Agenda for the Future.1型神经纤维瘤病相关恶性外周神经鞘膜瘤的科学现状:勾勒未来研究议程
J Natl Cancer Inst. 2017 Aug 1;109(8). doi: 10.1093/jnci/djx124.
2
Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas.成人软组织肉瘤的综合与整合基因组特征分析
Cell. 2017 Nov 2;171(4):950-965.e28. doi: 10.1016/j.cell.2017.10.014.
3
Pembrolizumab in advanced soft-tissue sarcoma and bone sarcoma (SARC028): a multicentre, two-cohort, single-arm, open-label, phase 2 trial.帕博利珠单抗治疗晚期软组织肉瘤和骨肉瘤(SARC028):一项多中心、双队列、单臂、开放标签的2期试验。
Lancet Oncol. 2017 Nov;18(11):1493-1501. doi: 10.1016/S1470-2045(17)30624-1. Epub 2017 Oct 4.
4
Use of PD-1 Targeting, Macrophage Infiltration, and IDO Pathway Activation in Sarcomas: A Phase 2 Clinical Trial.PD-1 靶向治疗、巨噬细胞浸润和 IDO 通路激活在肉瘤中的应用:一项 2 期临床试验。
JAMA Oncol. 2018 Jan 1;4(1):93-97. doi: 10.1001/jamaoncol.2017.1617.
5
Malignant Peripheral Nerve Sheath Tumors State of the Science: Leveraging Clinical and Biological Insights into Effective Therapies.恶性周围神经鞘膜瘤的科学现状:利用临床和生物学见解实现有效治疗
Sarcoma. 2017;2017:7429697. doi: 10.1155/2017/7429697. Epub 2017 May 16.
6
Histopathologic evaluation of atypical neurofibromatous tumors and their transformation into malignant peripheral nerve sheath tumor in patients with neurofibromatosis 1-a consensus overview.1型神经纤维瘤病患者非典型神经纤维瘤性肿瘤及其向恶性外周神经鞘瘤转化的组织病理学评估——共识综述
Hum Pathol. 2017 Sep;67:1-10. doi: 10.1016/j.humpath.2017.05.010. Epub 2017 May 24.
7
Histotype-tailored neoadjuvant chemotherapy versus standard chemotherapy in patients with high-risk soft-tissue sarcomas (ISG-STS 1001): an international, open-label, randomised, controlled, phase 3, multicentre trial.基于组织学分型的新辅助化疗对比标准化疗用于高危软组织肉瘤患者(ISG-STS 1001):一项国际、开放标签、随机、对照、III 期、多中心试验
Lancet Oncol. 2017 Jun;18(6):812-822. doi: 10.1016/S1470-2045(17)30334-0. Epub 2017 May 9.
8
T-cell infiltration and clonality correlate with programmed cell death protein 1 and programmed death-ligand 1 expression in patients with soft tissue sarcomas.T细胞浸润和克隆性与软组织肉瘤患者程序性细胞死亡蛋白1和程序性死亡配体1的表达相关。
Cancer. 2017 Sep 1;123(17):3291-3304. doi: 10.1002/cncr.30726. Epub 2017 May 2.
9
PDL1 expression is a poor-prognosis factor in soft-tissue sarcomas.程序性死亡配体1(PDL1)表达是软组织肉瘤的一个预后不良因素。
Oncoimmunology. 2017 Feb 8;6(3):e1278100. doi: 10.1080/2162402X.2016.1278100. eCollection 2017.
10
Patterns of care and outcomes of patients with METAstatic soft tissue SARComa in a real-life setting: the METASARC observational study.真实环境中转移性软组织肉瘤患者的治疗模式及结局:METASARC观察性研究
BMC Med. 2017 Apr 10;15(1):78. doi: 10.1186/s12916-017-0831-7.

未分化多形性肉瘤、黏液纤维肉瘤和恶性外周神经鞘瘤的生物学特性和治疗管理:现状与展望。

Biology and Management of Undifferentiated Pleomorphic Sarcoma, Myxofibrosarcoma, and Malignant Peripheral Nerve Sheath Tumors: State of the Art and Perspectives.

机构信息

Brigitte C. Widemann, National Cancer Institute, Bethesda, MD; and Antoine Italiano, Institut Bergonié and University of Bordeaux, Bordeaux, France.

出版信息

J Clin Oncol. 2018 Jan 10;36(2):160-167. doi: 10.1200/JCO.2017.75.3467. Epub 2017 Dec 8.

DOI:10.1200/JCO.2017.75.3467
PMID:29220302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5759316/
Abstract

Undifferentiated pleomorphic sarcomas, myxofibrosarcomas, and malignant peripheral nerve sheath tumors are characterized by complex genomic characteristics and aggressive clinical behavior. Recent advances in the understanding of the pathogenesis of these tumors may allow for the development of more-effective innovative therapeutic strategies, including immunotherapies. This review describes the current knowledge of the epidemiology, clinical presentation, treatment, and pathogenesis of these tumors and highlights ongoing and future research.

摘要

未分化多形性肉瘤、黏液纤维肉瘤和恶性外周神经鞘瘤的特征是具有复杂的基因组特征和侵袭性的临床行为。对这些肿瘤发病机制的认识的最新进展可能允许开发更有效的创新治疗策略,包括免疫疗法。本文描述了这些肿瘤的流行病学、临床表现、治疗和发病机制的现有知识,并强调了正在进行和未来的研究。