Updates on the Treatment of Tenosynovial Giant Cell Tumor.

Q1 Medicine
Abigail S Chan, Vatsala Katiyar, Paul Dy, Vikas Singh
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引用次数: 1

Abstract

Tenosynovial giant cell tumor (TGCT) is a rare inflammatory disorder affecting the joint synovium, bursae, and tendon sheaths that causes non-specific and often insidious joint discomfort. The application of systemic chemotherapy has been limited due to poor and unsustained disease responses. Surgery with or without adjuvant radiation is the primary treatment modality for TGCT. With its locally destructive nature and increased recurrence, multiple surgical interventions become necessary throughout the course of the disease, leading to disfigurement, decreased quality of life, and increased mortality. However, owing to recent evidence demonstrating the overexpression of colony-stimulating factor 1 (CSF-1) in TGCT, selective tyrosine kinase inhibitors targeting CSF-1 receptors are being developed. Pexidartinib is the first CSF-1 receptor inhibitor approved for the treatment of TGCT. Here, we discuss various available treatment strategies and ongoing investigations and trials targeting diffuse TGCT, which include nilotinib, lacnotuzumab, cabiralizumab, vimseltinib, and emactuzumab.

腱鞘巨细胞瘤的治疗进展。
腱鞘巨细胞瘤(TGCT)是一种罕见的炎症性疾病,影响关节滑膜、滑囊和肌腱鞘,引起非特异性且通常是隐匿的关节不适。由于不良和不持续的疾病反应,全身化疗的应用受到限制。手术加或不加辅助放疗是TGCT的主要治疗方式。由于其局部破坏性和复发率的增加,在整个疾病过程中需要多次手术干预,导致毁容,生活质量下降和死亡率增加。然而,由于最近有证据表明集落刺激因子1 (CSF-1)在TGCT中过表达,针对CSF-1受体的选择性酪氨酸激酶抑制剂正在开发中。培西达替尼是首个被批准用于治疗TGCT的CSF-1受体抑制剂。在这里,我们讨论了各种可用的治疗策略和正在进行的针对弥漫性TGCT的研究和试验,包括尼洛替尼、拉诺妥珠单抗、卡比利珠单抗、维姆seltinib和emactuzumab。
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
CiteScore
4.30
自引率
0.00%
发文量
0
审稿时长
27 weeks
期刊介绍: Hematology Oncology and Stem Cell Therapy is an international, peer-reviewed, open access journal that provides a vehicle for publications of high-quality clinical as well as basic science research reports in hematology and oncology. The contents of the journal also emphasize the growing importance of hematopoietic stem cell therapy for treatment of various benign and malignant hematologic disorders and certain solid tumors.The journal prioritizes publication of original research articles but also would give consideration for brief reports, review articles, special communications, and unique case reports. It also offers a special section for clinically relevant images that provide an important educational value.
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