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凡努西单抗的作用机制:血浆、肿瘤及皮肤伤口愈合活检中的系列生物标志物

Vanucizumab mode of action: Serial biomarkers in plasma, tumor, and skin-wound-healing biopsies.

作者信息

Heil Florian, Babitzki Galina, Julien-Laferriere Alice, Ooi Chia-Huey, Hidalgo Manuel, Massard Christophe, Martinez-Garcia Maria, Le Tourneau Christophe, Kockx Mark, Gerber Peter, Rossomanno Simona, Krieter Oliver, Lahr Angelika, Wild Norbert, Harring Suzana Vega, Lechner Katharina

机构信息

Roche Innovation Center Munich, Nonnenwald 2, 82377 Penzberg, Germany.

Soladis GmbH, Basel, Switzerland.

出版信息

Transl Oncol. 2021 Feb;14(2):100984. doi: 10.1016/j.tranon.2020.100984. Epub 2020 Dec 15.

DOI:10.1016/j.tranon.2020.100984
PMID:33338877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7749407/
Abstract

Vanucizumab is a novel bispecific antibody inhibiting vascular endothelial growth factor (VEGF-A) and angiopoietin-2 (Ang-2) that demonstrated safety and anti-tumor activity in part I of a phase I study of 42 patients with advanced solid tumors. Part II evaluated the pharmacodynamic effects of vanucizumab 30 or 15 mg/kg every 2 weeks in 32 patients. Serial plasma samples, paired tumor, and skin-wound-healing biopsies were taken over 29 days to evaluate angiogenic markers. Vanucizumab was associated with marked post-infusion reductions in circulating unbound VEGF-A and Ang-2. By day 29, tumor samples revealed mean reductions in density of microvessels (-32.2%), proliferating vessels (-47.9%) and Ang-2 positive vessels (-62.5%). Skin biopsies showed a mean reduction in density of microvessels (-49.0%) and proliferating vessels (-25.7%). Gene expression profiling of tumor samples implied recruitment and potential activation of lymphocytes. Biopsies were safely conducted. Vanucizumab demonstrated a consistent biological effect on vascular-related biomarkers, confirming proof of concept. Skin-wound-healing biopsies were a valuable surrogate for studying angiogenesis-related mechanisms.

摘要

凡努昔单抗是一种新型双特异性抗体,可抑制血管内皮生长因子(VEGF-A)和血管生成素-2(Ang-2),在一项针对42例晚期实体瘤患者的I期研究的第一部分中显示出安全性和抗肿瘤活性。第二部分评估了每2周给予30或15mg/kg凡努昔单抗对32例患者的药效学作用。在29天内采集系列血浆样本、配对肿瘤和皮肤伤口愈合活检样本,以评估血管生成标志物。凡努昔单抗与输注后循环中游离VEGF-A和Ang-2的显著降低有关。到第29天,肿瘤样本显示微血管密度(-32.2%)、增殖血管(-47.9%)和Ang-2阳性血管(-62.5%)平均降低。皮肤活检显示微血管密度(-49.0%)和增殖血管(-25.7%)平均降低。肿瘤样本的基因表达谱分析提示淋巴细胞的募集和潜在激活。活检操作安全。凡努昔单抗对血管相关生物标志物显示出一致的生物学效应,证实了概念验证。皮肤伤口愈合活检是研究血管生成相关机制的有价值替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/fb59e7f97c13/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/4997fa9fdc71/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/dd0982f88378/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/5678b64d54dc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/bd2969c5362a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/2445075f2467/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/a835f8490376/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/fb59e7f97c13/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/4997fa9fdc71/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/dd0982f88378/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/5678b64d54dc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/bd2969c5362a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/2445075f2467/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/a835f8490376/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3355/7749407/fb59e7f97c13/gr7.jpg

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