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April 5, 2026Cancer Research0 citations

Abstract 4400: Degrader antibody conjugates (DACs) as a next-generation therapeutic approach for selective and potent targeted protein degradation in EGFR-positive cancers

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JLJihye LeeSLSoohyun LeeJKJiyoung Kim

Key Points

  • The research aims to evaluate the efficacy and specificity of degrader antibody conjugates (DACs) in targeting EGFR-positive cancers.
  • Synthesis of DACs using diverse linker-payload designs.
  • Conjugation of DACs to cetuximab for targeted degradation.
  • Evaluation of DACs across multiple cell lines for potency and anti-proliferative activity.
  • In vivo pharmacodynamic studies to assess selective degradation in EGFR-positive versus EGFR-negative tissues.
  • Several DAC constructs showed significantly enhanced degradation efficiency compared to free payloads.
  • Improved inhibition of cellular proliferation was observed in EGFR-positive models.
  • Selective degradation of target protein was confirmed in EGFR-positive tissues with no degradation in EGFR-negative tissues.

Abstract

Abstract Antibody Drug Conjugates (ADCs) have become an established therapeutic modality in oncology; however, challenges such as payload-associated systemic toxicity and the emergence of resistance to conventional cytotoxic payloads underscore the need for next-generation payload. Degrader Antibody Conjugates (DACs) have recently attracted attention as an alternative strategy that leverages targeted protein degradation rather than traditional toxin-mediated cytotoxicity. In this study, we synthesized a panel of DACs by generating diverse linker-payload (LP) designs engineered for targeted degradation and conjugating them to cetuximab. These DACs were evaluated across multiple cell lines for their degradation potency and anti-proliferative activity. In several EGFR-positive models, specific DAC constructs demonstrated significantly enhanced degradation efficiency relative to the corresponding free payloads, accompanied by improved inhibition of cellular proliferation. In vivo pharmacodynamic studies confirmed selective degradation of the target protein in EGFR-positive tissues, whereas no degradation was detected in EGFR-negative tissues, demonstrating the high specificity of the DAC mechanism. Overall, our findings show that our DAC platform exhibits potent on-target antitumor activity in relevant indications while minimizing off-target toxicity in non-expressing tissues. These results establish a proof-of-concept for DACs as a safer and mechanistically differentiated therapeutic approach warranting further development. Citation Format: Jihye Lee, Soohyun Lee, Jiyoung Kim, Han Wool Kim, So Hyuk Kim, Onnuri Bae, Jeonghwa Han, Je Ho Ryu, Song Hee Lee. Degrader antibody conjugates (DACs) as a next-generation therapeutic approach for selective and potent targeted protein degradation in EGFR-positive cancers 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 4400.

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Cite This Study

Lee et al. (2026) studied this question.

synapsesocial.com/papers/69d1fd9ca79560c99a0a3b74https://doi.org/10.1158/1538-7445.am2026-4400
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