Abstract 2652: MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer

Abstract Background: Aberrant glycosylation is a hallmark of many malignancies, driving tumor growth, immune evasion, and metastasis. Certain tumor-associated glycans are highly expressed in small-cell lung cancer (SCLC) but minimally present in normal tissues, making them attractive yet underexplored targets for antibody-drug conjugates (ADCs). MGT-1142 is an exatecan-based ADC engineered with an optimized Fc domain to recognize a tumor-specific glycosylation pattern and selectively deliver a potent topoisomerase I inhibitor payload. Methods: Comprehensive in vitro and in vivo evaluations were performed to characterize MGT-1142. Binding affinity, internalization, and cytotoxicity were examined across multiple SCLC cell lines. Anti-tumor efficacy was assessed in both cell line-derived xenograft (CDX) and patient-derived xenograft (PDX) models. Pharmacokinetic (PK) and dose-range-finding (DRF) studies were conducted in cynomolgus monkeys to determine systemic exposure, half-life, and tolerability. Results: MGT-1142 exhibited high target specificity with no detectable cross-reactivity to structurally related glycans. It demonstrated strong binding and rapid internalization in glycan-positive cells, resulting in potent inhibition of antigen-positive tumor cell proliferation. In vivo, MGT-1142 achieved dose-dependent tumor growth inhibition across multiple CDX and PDX models. Cynomolgus PK studies revealed linear, dose-proportional exposure and a favorable terminal half-life. Dose range finding studies indicated good tolerability and a wide therapeutic window. Conclusions: MGT-1142 shows potent and selective anti-tumor activity, favorable pharmacokinetics, and an encouraging safety profile in preclinical studies. These findings support MGT-1142 as a potential first-in-class glycan-targeting ADC for the treatment of small-cell lung cancer. Citation Format: Su-Yu Tsai, Maomao He, Ju-Mei Li, Ping Chao, Ting-Chun Hung, Mei-Hsuan Tsai, Charng-Sheng Tsai. MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2652.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2652
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 2652: MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer

Ting-Chun Hung, Ping Chao, Su-Yu Tsai, Charng-Sheng Tsai et al.
Cancer Research
Glycosylation and Glycoproteins Research
article

Abstract 2652: MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer

Ting-Chun Hung, Ping Chao, Su-Yu Tsai, Charng-Sheng Tsai, Maomao He, Ju-Mei Li, Mei-Hsuan Tsai
article en

Abstract

Abstract Background: Aberrant glycosylation is a hallmark of many malignancies, driving tumor growth, immune evasion, and metastasis. Certain tumor-associated glycans are highly expressed in small-cell lung cancer (SCLC) but minimally present in normal tissues, making them attractive yet underexplored targets for antibody-drug conjugates (ADCs). MGT-1142 is an exatecan-based ADC engineered with an optimized Fc domain to recognize a tumor-specific glycosylation pattern and selectively deliver a potent topoisomerase I inhibitor payload. Methods: Comprehensive in vitro and in vivo evaluations were performed to characterize MGT-1142. Binding affinity, internalization, and cytotoxicity were examined across multiple SCLC cell lines. Anti-tumor efficacy was assessed in both cell line-derived xenograft (CDX) and patient-derived xenograft (PDX) models. Pharmacokinetic (PK) and dose-range-finding (DRF) studies were conducted in cynomolgus monkeys to determine systemic exposure, half-life, and tolerability. Results: MGT-1142 exhibited high target specificity with no detectable cross-reactivity to structurally related glycans. It demonstrated strong binding and rapid internalization in glycan-positive cells, resulting in potent inhibition of antigen-positive tumor cell proliferation. In vivo, MGT-1142 achieved dose-dependent tumor growth inhibition across multiple CDX and PDX models. Cynomolgus PK studies revealed linear, dose-proportional exposure and a favorable terminal half-life. Dose range finding studies indicated good tolerability and a wide therapeutic window. Conclusions: MGT-1142 shows potent and selective anti-tumor activity, favorable pharmacokinetics, and an encouraging safety profile in preclinical studies. These findings support MGT-1142 as a potential first-in-class glycan-targeting ADC for the treatment of small-cell lung cancer. Citation Format: Su-Yu Tsai, Maomao He, Ju-Mei Li, Ping Chao, Ting-Chun Hung, Mei-Hsuan Tsai, Charng-Sheng Tsai. MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2652.

Cancer ResearchVol. 86(7_Supplement)
The Marigold Foundation (CA)
Good health and well-being
Openalex Percentile: Top 8%
Glycosylation and Glycoproteins Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.