• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

难治性非小细胞肺癌中补体因子H靶向抗体GT103:一项1b期剂量递增试验

Complement factor H targeting antibody GT103 in refractory non-small cell lung cancer: a phase 1b dose escalation trial.

作者信息

Clarke Jeffrey M, Simon George R, Mamdani Hirva, Gu Lin, Herndon James E, Stinchcombe Thomas E, Ready Neal, Crawford Jeffrey, Sonpavde Guru, Balevic Stephen, Nixon Andrew B, Campa Michael, Gottlin Elizabeth B, Li Huihua, Saxena Ruchi, He You Wen, Antonia Scott, Patz Edward F

机构信息

Duke Cancer Institute, Durham, NC, USA.

Duke University School of Medicine, Durham, NC, USA.

出版信息

Nat Commun. 2025 Jan 2;16(1):93. doi: 10.1038/s41467-024-55092-2.

DOI:10.1038/s41467-024-55092-2
PMID:39747856
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11695982/
Abstract

GT103 is a first-in-class, fully human, IgG3 monoclonal antibody targeting complement factor H that kills tumor cells and promotes anti-cancer immunity in preclinical models. We conducted a first-in-human phase 1b study dose escalation trial of GT103 in refractory non-small cell lung cancer to assess the safety of GT103 (NCT04314089). Dose escalation was performed using a "3 + 3" schema with primary objectives of determining safety, tolerability, PK profile and maximum tolerated dose (MTD) of GT103. Secondary objectives included describing objective response rate, progression-free survival and overall survival. Dose escalation cohorts included GT103 given intravenously at 0.3, 1, 3, 10, and 15 mg/kg every 3 weeks, and 10 mg/kg every 2 weeks. Thirty one patients were enrolled across 3 institutions. Two dose-limiting adverse events were reported: grade 3 acute kidney injury (0.3 mg/kg) and grade 2 colitis (1 mg/kg). No dose-limiting toxicities were noted at the highest dose levels and the MTD was not reached. No objective responses were seen. Stable disease occurred in 9 patients (29%) and the median overall survival was 25.7 weeks (95% confidence interval [CI], 19.1-30.6). Pharmacokinetic analysis confirmed an estimated half life of 6.5 days. The recommended phase 2 dose of GT103 was 10 mg/kg every 3 weeks, however further dose optimization is needed given the absence of an MTD. The study achieved its primary objective of demonstrating safety and tolerability of GT103 in refractory NSCLC.

摘要

GT103是一种一流的全人源IgG3单克隆抗体,靶向补体因子H,在临床前模型中可杀死肿瘤细胞并促进抗癌免疫。我们开展了GT103用于难治性非小细胞肺癌的首次人体1b期剂量递增试验,以评估GT103的安全性(NCT04314089)。采用“3+3”方案进行剂量递增,主要目的是确定GT103的安全性、耐受性、药代动力学特征和最大耐受剂量(MTD)。次要目的包括描述客观缓解率、无进展生存期和总生存期。剂量递增队列包括每3周静脉注射0.3、1、3、10和15mg/kg的GT103,以及每2周静脉注射10mg/kg的GT103。3个机构共纳入了31例患者。报告了2例剂量限制不良事件:3级急性肾损伤(0.3mg/kg)和2级结肠炎(1mg/kg)。在最高剂量水平未观察到剂量限制毒性,未达到MTD。未观察到客观缓解。9例患者(29%)病情稳定,中位总生存期为25.7周(95%置信区间[CI],19.1-30.6)。药代动力学分析证实估计半衰期为6.5天。GT103的推荐2期剂量为每3周10mg/kg,然而鉴于未达到MTD,需要进一步优化剂量。该研究实现了其主要目标,即证明GT103在难治性非小细胞肺癌中的安全性和耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/b5272aba85f4/41467_2024_55092_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/1d5b139ab0b6/41467_2024_55092_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/c2eaa4e3e46a/41467_2024_55092_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/b5272aba85f4/41467_2024_55092_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/1d5b139ab0b6/41467_2024_55092_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/c2eaa4e3e46a/41467_2024_55092_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9e/11695982/b5272aba85f4/41467_2024_55092_Fig3_HTML.jpg

相似文献

1
Complement factor H targeting antibody GT103 in refractory non-small cell lung cancer: a phase 1b dose escalation trial.难治性非小细胞肺癌中补体因子H靶向抗体GT103:一项1b期剂量递增试验
Nat Commun. 2025 Jan 2;16(1):93. doi: 10.1038/s41467-024-55092-2.
2
Safety and antitumour activity of durvalumab plus tremelimumab in non-small cell lung cancer: a multicentre, phase 1b study.度伐利尤单抗联合曲美木单抗治疗非小细胞肺癌的安全性和抗肿瘤活性:一项多中心1b期研究
Lancet Oncol. 2016 Mar;17(3):299-308. doi: 10.1016/S1470-2045(15)00544-6. Epub 2016 Feb 6.
3
Anti-TIGIT Antibody Tiragolumab Alone or With Atezolizumab in Patients With Advanced Solid Tumors: A Phase 1a/1b Nonrandomized Controlled Trial.抗 TIGIT 抗体替利珠单抗单药或与阿替利珠单抗联合治疗晚期实体瘤患者的 1a/1b 期非随机对照试验。
JAMA Oncol. 2023 Nov 1;9(11):1574-1582. doi: 10.1001/jamaoncol.2023.3867.
4
Ramucirumab plus pembrolizumab in patients with previously treated advanced non-small-cell lung cancer, gastro-oesophageal cancer, or urothelial carcinomas (JVDF): a multicohort, non-randomised, open-label, phase 1a/b trial.雷莫芦单抗联合帕博利珠单抗治疗既往治疗的晚期非小细胞肺癌、胃食管交界处癌或尿路上皮癌患者(JVDF):一项多队列、非随机、开放标签、1a/1b 期临床试验。
Lancet Oncol. 2019 Aug;20(8):1109-1123. doi: 10.1016/S1470-2045(19)30458-9. Epub 2019 Jul 10.
5
Phase 1 dose escalation study of seribantumab (MM-121), an anti-HER3 monoclonal antibody, in patients with advanced solid tumors.一项评估抗 HER3 单克隆抗体 seribantumab(MM-121)在晚期实体瘤患者中安全性、耐受性和药代动力学的 1 期剂量递增研究。
Invest New Drugs. 2021 Dec;39(6):1604-1612. doi: 10.1007/s10637-021-01145-y. Epub 2021 Jul 11.
6
A phase I, open-label, multicentre, first-in-human study to evaluate safety, pharmacokinetics and efficacy of AMG 404, a PD-1 inhibitor, in patients with advanced solid tumours.一项I期、开放标签、多中心、首次人体研究,旨在评估PD-1抑制剂AMG 404在晚期实体瘤患者中的安全性、药代动力学和疗效。
BMJ Open. 2025 May 2;15(5):e088578. doi: 10.1136/bmjopen-2024-088578.
7
Evorpacept alone and in combination with pembrolizumab or trastuzumab in patients with advanced solid tumours (ASPEN-01): a first-in-human, open-label, multicentre, phase 1 dose-escalation and dose-expansion study.依维莫司联合帕博利珠单抗或曲妥珠单抗治疗晚期实体瘤患者的 ASPEN-01 研究:一项首次人体、开放标签、多中心、1 期剂量递增和剂量扩展研究。
Lancet Oncol. 2021 Dec;22(12):1740-1751. doi: 10.1016/S1470-2045(21)00584-2. Epub 2021 Nov 15.
8
Rovalpituzumab tesirine, a DLL3-targeted antibody-drug conjugate, in recurrent small-cell lung cancer: a first-in-human, first-in-class, open-label, phase 1 study.洛伐匹妥珠单抗替西瑞林,一种靶向DLL3的抗体药物偶联物,用于复发性小细胞肺癌:一项首次人体、同类首创、开放标签的1期研究。
Lancet Oncol. 2017 Jan;18(1):42-51. doi: 10.1016/S1470-2045(16)30565-4. Epub 2016 Dec 5.
9
MABp1, a first-in-class true human antibody targeting interleukin-1α in refractory cancers: an open-label, phase 1 dose-escalation and expansion study.MABp1,一种针对难治性癌症的首创类真正人源抗白细胞介素-1α 抗体:一项开放标签、1 期剂量递增和扩展研究。
Lancet Oncol. 2014 May;15(6):656-66. doi: 10.1016/S1470-2045(14)70155-X. Epub 2014 Apr 17.
10
Phase 1 dose-escalation study of mirvetuximab soravtansine (IMGN853), a folate receptor α-targeting antibody-drug conjugate, in patients with solid tumors.mirvetuximab soravtansine(IMGN853),一种靶向叶酸受体α的抗体药物偶联物,在实体瘤患者中的1期剂量递增研究。
Cancer. 2017 Aug 15;123(16):3080-3087. doi: 10.1002/cncr.30736. Epub 2017 Apr 25.

引用本文的文献

1
Serum Complement Factor H: A Marker for Progression and Outcome Prediction Towards Immunotherapy in Cutaneous Squamous Cell Carcinoma.血清补体因子H:皮肤鳞状细胞癌免疫治疗进展及预后预测的标志物
Cancers (Basel). 2025 Jun 26;17(13):2162. doi: 10.3390/cancers17132162.
2
Targeting the complement system: notes on therapeutic strategies for renal cancer.靶向补体系统:肾癌治疗策略笔记
Future Med Chem. 2025 May;17(9):979-981. doi: 10.1080/17568919.2025.2498876. Epub 2025 Apr 25.

本文引用的文献

1
Promotion of an Antitumor Immune Program by a Tumor-specific, Complement-activating Antibody.肿瘤特异性补体激活抗体促进抗肿瘤免疫程序。
J Immunol. 2024 May 15;212(10):1589-1601. doi: 10.4049/jimmunol.2300728.
2
Complement is activated by elevated IgG3 hexameric platforms and deposits C4b onto distinct antibody domains.补体通过升高的 IgG3 六聚体平台被激活,并将 C4b 沉积到不同的抗体结构域上。
Nat Commun. 2023 Jul 7;14(1):4027. doi: 10.1038/s41467-023-39788-5.
3
Antitumor Immune Mechanisms of the Anti-Complement Factor H Antibody GT103.
抗补体因子 H 抗体 GT103 的抗肿瘤免疫机制。
Mol Cancer Ther. 2023 Jun 1;22(6):778-789. doi: 10.1158/1535-7163.MCT-22-0723.
4
Pembrolizumab Plus Pemetrexed and Platinum in Nonsquamous Non-Small-Cell Lung Cancer: 5-Year Outcomes From the Phase 3 KEYNOTE-189 Study.帕博利珠单抗联合培美曲塞和铂类化疗用于非鳞状非小细胞肺癌:III 期 KEYNOTE-189 研究的 5 年结果。
J Clin Oncol. 2023 Apr 10;41(11):1992-1998. doi: 10.1200/JCO.22.01989. Epub 2023 Feb 21.
5
Pembrolizumab Plus Chemotherapy in Squamous Non-Small-Cell Lung Cancer: 5-Year Update of the Phase III KEYNOTE-407 Study.帕博利珠单抗联合化疗治疗鳞状非小细胞肺癌:III 期 KEYNOTE-407 研究的 5 年更新结果。
J Clin Oncol. 2023 Apr 10;41(11):1999-2006. doi: 10.1200/JCO.22.01990. Epub 2023 Feb 3.
6
Silencing EGFR-upregulated expression of CD55 and CD59 activates the complement system and sensitizes lung cancer to checkpoint blockade.沉默 EGFR 上调的 CD55 和 CD59 的表达可激活补体系统,并使肺癌对检查点阻断敏感。
Nat Cancer. 2022 Oct;3(10):1192-1210. doi: 10.1038/s43018-022-00444-4. Epub 2022 Oct 21.
7
Prognostic significance of a complement factor H autoantibody in early stage NSCLC.早期非小细胞肺癌中补体因子 H 自身抗体的预后意义。
Cancer Biomark. 2022;34(3):385-392. doi: 10.3233/CBM-210355.
8
The foundations of immune checkpoint blockade and the ipilimumab approval decennial.免疫检查点阻断的基础和伊匹单抗批准的十年。
Nat Rev Drug Discov. 2022 Jul;21(7):509-528. doi: 10.1038/s41573-021-00345-8. Epub 2021 Dec 22.
9
Tumour extracellular vesicle-derived Complement Factor H promotes tumorigenesis and metastasis by inhibiting complement-dependent cytotoxicity of tumour cells.肿瘤细胞外囊泡衍生的补体因子 H 通过抑制肿瘤细胞补体依赖性细胞毒性促进肿瘤发生和转移。
J Extracell Vesicles. 2020 Nov;10(1):e12031. doi: 10.1002/jev2.12031. Epub 2020 Nov 28.
10
Integrative Analysis of Complement System to Prognosis and Immune Infiltrating in Colon Cancer and Gastric Cancer.补体系统对结肠癌和胃癌预后及免疫浸润的综合分析
Front Oncol. 2021 Feb 3;10:553297. doi: 10.3389/fonc.2020.553297. eCollection 2020.