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通过精准引导治疗实现的mRCC患者的卓越反应,该治疗包括使用替西罗莫司和贝伐单抗进行免疫治疗再激发。

Exceptional Response in a Patient with mRCC Through Precision-Guided Treatment Involving Immunotherapy Rechallenge with Temsirolimus and Bevacizumab.

作者信息

Adibi Ashkan, Tokat Ünal Metin, Aydın Esranur, Özgü Eylül, Bilgiç Şevval Nur, Babacan Nalan Akgül, Tutar Onur, Kurzrock Razelle, Demiray Mutlu

机构信息

Precision Oncology Center, Medicana Health Group, Istanbul, Türkiye.

Department of Basic Oncology, Division of Cancer Genetics, Institute of Oncology, University of Istanbul, Istanbul, Türkiye.

出版信息

J Immunother Precis Oncol. 2025 May 12;8(2):184-190. doi: 10.36401/JIPO-25-3. eCollection 2025 May.

DOI:10.36401/JIPO-25-3
PMID:40376550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12080210/
Abstract

Comprehensive genomic profiling (CGP) and the subsequent discussions in molecular tumor boards (MTBs) are becoming an integral part of personalized cancer care. The patient with metastatic renal cell carcinoma (mRCC) presented here demonstrated an absence of a favorable response accompanied by adverse events after receiving dual immunotherapy with nivolumab plus ipilimumab in combination with a poly (adenosine diphosphate-ribose) polymerase inhibitor, niraparib. This determination was made based on the initial CGP report and the initial MTB. Following the progression of the disease and the emergence of immune-related adverse events, a second CGP was conducted, and several subsequent MTBs were held. The decision was made to transition the patient's treatment to temsirolimus plus bevacizumab, with the rechallenge of immunotherapy with pembrolizumab. The response evaluation revealed a complete radiographic and molecular response. This case study underscores the mounting significance of precision oncology in the management of mRCC, thereby suggesting that mammalian target of rapamycin inhibitor may augment the efficacy of immunotherapy in select patients based on their genomic findings. A digital poster of this case is included in the supplemental materials.

摘要

综合基因组分析(CGP)以及随后在分子肿瘤学委员会(MTB)中的讨论正成为个性化癌症治疗的一个组成部分。本文介绍的转移性肾细胞癌(mRCC)患者在接受纳武利尤单抗加伊匹木单抗联合聚(腺苷二磷酸 - 核糖)聚合酶抑制剂尼拉帕利的双重免疫治疗后,未出现良好反应且伴有不良事件。这一判定是基于初始的CGP报告和首次MTB讨论做出的。在疾病进展和免疫相关不良事件出现后,进行了第二次CGP分析,并召开了数次后续的MTB会议。决定将患者的治疗方案转换为替西罗莫司加贝伐单抗,并再次使用帕博利珠单抗进行免疫治疗。疗效评估显示出影像学和分子水平的完全缓解。本病例研究强调了精准肿瘤学在mRCC治疗中的重要性日益增加,从而表明雷帕霉素靶蛋白抑制剂可能根据患者的基因组结果增强免疫疗法在特定患者中的疗效。本病例的数字海报包含在补充材料中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/56b1f894a05a/i2590-017X-8-2-184-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/90ecb7be0ced/i2590-017X-8-2-184-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/bceaf1b12324/i2590-017X-8-2-184-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/56b1f894a05a/i2590-017X-8-2-184-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/90ecb7be0ced/i2590-017X-8-2-184-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/bceaf1b12324/i2590-017X-8-2-184-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30a7/12080210/56b1f894a05a/i2590-017X-8-2-184-f03.jpg

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Personalized Immunotherapy Achieves Complete Response in Metastatic Adenoid Cystic Carcinoma Despite Lack of Conventional Biomarkers.尽管缺乏常规生物标志物,个性化免疫疗法在转移性腺样囊性癌中实现完全缓解。
Curr Oncol. 2024 Sep 29;31(10):5838-5849. doi: 10.3390/curroncol31100434.
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Safety of immune checkpoint inhibitor rechallenge after severe immune-related adverse events: a retrospective analysis.
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Front Oncol. 2024 Jul 8;14:1403658. doi: 10.3389/fonc.2024.1403658. eCollection 2024.
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Front Endocrinol (Lausanne). 2024 Jan 31;15:1304188. doi: 10.3389/fendo.2024.1304188. eCollection 2024.
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