Literature DB >> 30359534

Antibody drug conjugates under investigation in phase I and phase II clinical trials for gastrointestinal cancer.

Alexis D Leal1, Anuradha Krishnamurthy1, Lia Head2, Wells A Messersmith1.   

Abstract

INTRODUCTION: Antibody drug conjugates (ADCs) represent a developing class of anticancer therapeutics which are designed to selectively deliver a cytotoxic payload to tumors, while limiting systemic toxicity to healthy tissues. There are several ADCs which are currently in various stages of clinical development for the treatment of gastrointestinal malignancies. AREAS COVERED: We discuss the biologic rationale and review the clinical experience with ADCs in the treatment of gastrointestinal malignancies, summarizing the pre-clinical and phase I/II clinical trial data that have been completed or are ongoing. EXPERT OPINION: While there have been significant advances in the development of ADCs since they were first introduced, several challenges remain. These challenges include (i) the selection of an ideal antigen target which is tumor specific and internalized upon binding, (ii) selection of an antibody which has high affinity for its antigen target and low immunogenicity, (iii) selection of a potent payload which is cytotoxic at sub-nanomolar concentrations, and (iv) optimal design of a linker to confer ADC stability with limited off-site toxicity. Efforts are ongoing to address these issues and innovate the ADC technology to improve the safety and efficacy of these agents.

Entities:  

Keywords:  Adenocarcinoma; antibody drug conjugate; cholangiocarcinoma; colorectal cancer; drug conjugates; esophageal cancer; gastric cancer; gastrointestinal malignancies; immunoconjugates; pancreatic cancer

Mesh:

Substances:

Year:  2018        PMID: 30359534     DOI: 10.1080/13543784.2018.1541085

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  4 in total

1.  HER2-targeted antibody-drug conjugate induces host immunity against cancer stem cells.

Authors:  Leiming Xia; Lu Wen; You Qin; Hannah E Dobson; Tao Zhang; Frank I Comer; Mary Jane Hinrichs; Michael D Oberst; Steven R Coats; Alfred E Chang; Yuanyuan Liu; Yangyi Bao; Fu Dai; Max S Wicha; Qiao Li
Journal:  Cell Chem Biol       Date:  2021-03-11       Impact factor: 8.116

2.  Phase I study of the recombinant humanized anti-HER2 monoclonal antibody-MMAE conjugate RC48-ADC in patients with HER2-positive advanced solid tumors.

Authors:  Yingying Xu; Yakun Wang; Jifang Gong; Xiaotian Zhang; Zhi Peng; Xinan Sheng; Chenyu Mao; Qingxia Fan; Yuxian Bai; Yi Ba; Da Jiang; Fen Yang; Changsong Qi; Jian Li; Xicheng Wang; Jun Zhou; Ming Lu; Yanshuo Cao; Jiajia Yuan; Dan Liu; Zhenghang Wang; Jianmin Fang; Lin Shen
Journal:  Gastric Cancer       Date:  2021-05-04       Impact factor: 7.701

3.  Incorporation of a Hydrophilic Spacer Reduces Hepatic Uptake of HER2-Targeting Affibody-DM1 Drug Conjugates.

Authors:  Haozhong Ding; Mohamed Altai; Sara S Rinne; Anzhelika Vorobyeva; Vladimir Tolmachev; Torbjörn Gräslund; Anna Orlova
Journal:  Cancers (Basel)       Date:  2019-08-14       Impact factor: 6.639

4.  Site-Specific, Stoichiometric-Controlled, PEGylated Conjugates of Fibroblast Growth Factor 2 (FGF2) with Hydrophilic Auristatin Y for Highly Selective Killing of Cancer Cells Overproducing Fibroblast Growth Factor Receptor 1 (FGFR1).

Authors:  Mateusz Adam Krzyscik; Małgorzata Zakrzewska; Jacek Otlewski
Journal:  Mol Pharm       Date:  2020-06-16       Impact factor: 4.939

  4 in total

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