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依维莫司治疗侵袭性恶性肾上皮样血管平滑肌脂肪瘤

Everolimus in Invasive Malignant Renal Epithelioid Angiomyolipoma.

作者信息

Guo Gang, Gu Liangyou, Zhang Xu

机构信息

Department of Urology, The Third Medical Centre, Chinese PLA General Hospital, Beijing, China.

出版信息

Front Oncol. 2021 Jan 26;10:610858. doi: 10.3389/fonc.2020.610858. eCollection 2020.

Abstract

BACKGROUND

To evaluate the efficacy and safety of everolimus, a mTOR inhibitor, on invasive malignant renal epithelioid angiomyolipoma (EAML).

MATERIALS AND METHODS

From Oct 2014 to May 2019, we collected data from seven patients with a definite (clinical and pathological) diagnosis of EAML received everolimus in our hospital. Targeted sequence capture array technique with next-generation of high throughput sequencing (NGS) were performed to detect mutations of TSC1/2 genes. All patients had received surgery and everolimus. The clinical efficacy and safety of the therapy were evaluated.

RESULTS

Mutations of TSC1 and TSC2 were detected in two and three patients though targeted sequence capture array technique with NGS, respectively. Among seven patients, three had missense mutations, one had nonsense mutation, and one had the large fragment deletion mutation. Five patients accompanied with tuberous sclerosis complex (TSC) were identified. All patients were administered 10mg everolimus once daily, the treatment duration lasted for 3 to 28 months. The objective response was assessed 3 months later, five partial response, two stable disease (SD), the mean greatest tumor diameter of all patients decreased from 9.6 to 5.2cm. Six patients stayed SD and one patient died during follow up. Patients accompanying with TSC had better responses to everolimus compared with non-TSC.

CONCLUSION

The mTOR inhibitor can be an effective treatment for patients with invasive malignant renal EAML. Patients with TSC may benefit more from the therapy.

摘要

背景

评估mTOR抑制剂依维莫司对侵袭性恶性肾上皮样血管平滑肌脂肪瘤(EAML)的疗效和安全性。

材料与方法

2014年10月至2019年5月,我们收集了我院7例确诊(临床和病理)为EAML且接受依维莫司治疗的患者的数据。采用靶向序列捕获阵列技术结合新一代高通量测序(NGS)检测TSC1/2基因的突变。所有患者均接受了手术及依维莫司治疗。评估该治疗方法的临床疗效和安全性。

结果

通过NGS靶向序列捕获阵列技术,分别在2例和3例患者中检测到TSC1和TSC2的突变。7例患者中,3例为错义突变,1例为无义突变,1例为大片段缺失突变。鉴定出5例伴有结节性硬化症(TSC)的患者。所有患者均接受每日一次10mg依维莫司治疗,治疗持续时间为3至28个月。3个月后评估客观缓解情况,5例部分缓解,2例病情稳定(SD),所有患者的平均最大肿瘤直径从9.6cm降至5.2cm。随访期间,6例患者病情稳定,1例患者死亡。伴有TSC的患者对依维莫司的反应比非TSC患者更好。

结论

mTOR抑制剂可有效治疗侵袭性恶性肾EAML患者。伴有TSC的患者可能从该治疗中获益更多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9fe/7870865/8f893e251de5/fonc-10-610858-g001.jpg

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