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纤维瘤病的治疗是否开始渐入佳境?

Are the Pieces Starting to Come Together for Management of Desmoid Tumors?

机构信息

Desmoid Tumor Research Foundation, Suffern, New York.

Washington University in St. Louis, School of Medicine, Department of Medicine, Division of Medical Oncology, St. Louis, Missouri.

出版信息

Clin Cancer Res. 2022 Sep 15;28(18):3911-3913. doi: 10.1158/1078-0432.CCR-22-0620.

DOI:10.1158/1078-0432.CCR-22-0620
PMID:35819317
Abstract

Desmoid tumor research is changing how desmoid tumors are managed with the prospective documentation that growing desmoid tumors spontaneously regress one third of the time. Patient partnership through the Desmoid Research Tumor Foundation and academia is leading to rapid advancement in desmoid tumor biology understanding and treatment. See related articles by Colombo et al., p. 4027, Nathenson et al., p. 4092, and Penel et al., p. 4105.

摘要

研究表明,生长中的硬纤维瘤有三分之一会自发消退,前瞻性的文献记录正在改变硬纤维瘤的管理方式。通过硬纤维瘤研究肿瘤基金会和学术界的患者合作,正在推动硬纤维瘤生物学理解和治疗方面的快速进展。请参阅 Colombo 等人的相关文章,第 4027 页,Nathenson 等人的第 4092 页,以及 Penel 等人的第 4105 页。

相似文献

1
Are the Pieces Starting to Come Together for Management of Desmoid Tumors?纤维瘤病的治疗是否开始渐入佳境?
Clin Cancer Res. 2022 Sep 15;28(18):3911-3913. doi: 10.1158/1078-0432.CCR-22-0620.
2
Detection of beta-catenin mutations in paraffin-embedded sporadic desmoid-type fibromatosis by mutation-specific restriction enzyme digestion (MSRED): an ancillary diagnostic tool.通过突变特异性限制性酶切(MSRED)检测石蜡包埋的散发性硬纤维瘤型纤维瘤病中的β-连环蛋白突变:一种辅助诊断工具。
Am J Surg Pathol. 2007 Sep;31(9):1299-309. doi: 10.1097/PAS.0b013e31802f581a.
3
The Evolving Management of Desmoid Fibromatosis.韧带样纤维瘤病的管理进展
Surg Clin North Am. 2022 Aug;102(4):667-677. doi: 10.1016/j.suc.2022.05.005.
4
Is mutation analysis of β-catenin useful for the diagnosis of desmoid-type fibromatosis? A systematic review.β-连环蛋白突变分析对诊断硬纤维瘤型纤维瘤病是否有用?系统评价。
Jpn J Clin Oncol. 2020 Sep 5;50(9):1037-1042. doi: 10.1093/jjco/hyaa080.
5
Extra-abdominal desmoid fibromatosis: A review of management, current guidance and unanswered questions.腹外硬纤维瘤病:治疗、当前指南及未解决问题综述
Eur J Surg Oncol. 2016 Jul;42(7):1071-83. doi: 10.1016/j.ejso.2016.02.012. Epub 2016 Feb 19.
6
Whole-Genome and Transcriptome Sequencing Identified NOTCH2 and HES1 as Potential Markers of Response to Imatinib in Desmoid Tumor (Aggressive Fibromatosis): A Phase II Trial Study.全基因组和转录组测序鉴定 NOTCH2 和 HES1 作为伊马替尼治疗侵袭性纤维瘤病(硬纤维瘤)反应的潜在标志物:一项 II 期试验研究。
Cancer Res Treat. 2022 Oct;54(4):1240-1255. doi: 10.4143/crt.2021.1194. Epub 2022 Jan 17.
7
Cutaneous desmoid-type fibromatosis: A rare case with molecular profiling.皮肤韧带样型纤维瘤病:一例罕见的分子特征分析病例
J Cutan Pathol. 2021 Sep;48(9):1185-1188. doi: 10.1111/cup.14058. Epub 2021 Jun 30.
8
Molecular Pathogenesis of Sporadic Desmoid Tumours and Its Implications for Novel Therapies: A Systematised Narrative Review.散发性硬纤维瘤的分子发病机制及其对新型治疗方法的启示:系统叙述性综述。
Target Oncol. 2022 May;17(3):223-252. doi: 10.1007/s11523-022-00876-z. Epub 2022 Apr 21.
9
CTNNB1 S45F mutation predicts poor efficacy of meloxicam treatment for desmoid tumors: a pilot study.CTNNB1 S45F突变预示美洛昔康治疗硬纤维瘤疗效不佳:一项初步研究
PLoS One. 2014 May 1;9(5):e96391. doi: 10.1371/journal.pone.0096391. eCollection 2014.
10
A rare sporadic pancreatic desmoid fibromatosis diagnosed by endoscopic ultrasound-guided fine-needle aspiration: Case report and literature review.经内镜超声引导下细针抽吸术诊断的罕见散发型胰腺硬纤维瘤病:病例报告及文献复习。
Diagn Cytopathol. 2021 Feb;49(2):E49-E54. doi: 10.1002/dc.24580. Epub 2020 Aug 28.

引用本文的文献

1
MRI T2 mapping assessment of T2 relaxation time in desmoid tumors as a quantitative imaging biomarker of tumor response: preliminary results.MRI T2 映射评估韧带样瘤中 T2 弛豫时间作为肿瘤反应的定量成像生物标志物:初步结果
Front Oncol. 2023 Dec 22;13:1286807. doi: 10.3389/fonc.2023.1286807. eCollection 2023.
2
Case Report: Desmoid fibromatosis in the mediastinum of a 6-month-old toddler, what to do?病例报告:一名6个月大幼儿纵隔内的硬纤维瘤病,该如何处理?
Front Surg. 2023 Jan 30;9:1007760. doi: 10.3389/fsurg.2022.1007760. eCollection 2022.