Suppr超能文献

转移性基底细胞癌在 hedgehog 信号通路抑制剂时代。

Metastatic basal cell carcinoma in the era of hedgehog signaling pathway inhibitors.

机构信息

Virginia G. Piper Cancer Center Clinical Trials at Scottsdale Healthcare, Scottsdale, Arizona; Translational Genomics Research Institute, Phoenix, AZ 85258, USA.

出版信息

Cancer. 2012 Nov 1;118(21):5310-9. doi: 10.1002/cncr.27532. Epub 2012 Apr 17.

Abstract

Inhibition of the hedgehog signaling pathway (HHSP) for the treatment of locally advanced basal cell carcinoma (BCC) and metastatic BCC (mBCC) has produced promising results. Typically, mBCC is not taken into consideration during the workup of a patient with multifocal metastatic disease who has a history of BCC. The objective of the current review, in which the authors evaluated the time from the first BCC diagnosis to metastasis, location of disease, and radiographic features, was to contribute to the general knowledge and awareness among providers, patients, and support groups about mBCC and to provide an outlook for the future of treatments for mBCC. A literature review on mBCC and a review of records from patients with mBCC who presented to Virginia G. Piper Cancer Center Clinical Trials (an oncology clinical trials center) were conducted. The clinical and radiographic findings of 22 patients with mBCC who were evaluated at that center from the initiation of smoothened (SMO) antagonist trials were analyzed along with a review of BCC epidemiology and pathogenesis, the HHSP, and current and future treatments for this rare presentation of the most common malignancy. The results indicated that, in the last 5 years, there has been a plethora of new agents targeting SMO, a key component of the HHSP that, for the majority of patients with mBCC, may be a good match for targeting tumor genetic vulnerability. Like with other targeted therapy for uncommon malignancies, such as chronic myelogenous leukemia and gastrointestinal stromal tumors, the authors anticipate that there will be clinical development of next-generation HHSP inhibitors to combat mBCCs that are nonresponsive to or progress on current SMO antagonists.

摘要

抑制刺猬信号通路(HHSP)可治疗局部晚期基底细胞癌(BCC)和转移性 BCC(mBCC),已取得可喜的成果。通常情况下,对于患有多发性转移性疾病且有 BCC 病史的患者,在进行检查时不会考虑 mBCC。作者评估了从首次 BCC 诊断到转移的时间、疾病部位和影像学特征,其目的是增进提供者、患者和支持团体对 mBCC 的一般认识和了解,并为 mBCC 的未来治疗提供展望。作者对 mBCC 进行了文献回顾,并对在弗吉尼亚 G. 派珀癌症中心临床研究(肿瘤临床研究中心)就诊的 mBCC 患者的记录进行了审查。对在该中心接受 smoothened(SMO)拮抗剂试验启动后评估的 22 名 mBCC 患者的临床和影像学发现进行了分析,并回顾了 BCC 的流行病学和发病机制、HHSP 以及当前和未来针对这种最常见恶性肿瘤罕见表现的治疗方法。结果表明,在过去 5 年中,已有大量新的靶向 SMO 的药物问世,SMO 是 HHSP 的关键组成部分,对于大多数 mBCC 患者来说,靶向肿瘤遗传易感性可能是一个很好的选择。与其他针对罕见恶性肿瘤(如慢性髓性白血病和胃肠道间质瘤)的靶向治疗一样,作者预计将开发新一代 HHSP 抑制剂,以对抗对当前 SMO 拮抗剂无反应或进展的 mBCC。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验