Determinants of long-term response to patritumab deruxtecan in breast cancer patient-derived xenografts

Novel antibody-drug conjugates (ADCs) have shown potent antitumor activity across multiple cancer types. However, the key determinants of therapeutic response remain under investigation. In this study, we aimed to identify potential determinants of long-term response to patritumab deruxtecan (HER3-DXd; MK-1022), a HER3-directed ADC linked to a potent topoisomerase I inhibitor (TOP1i) payload, using a cohort of thirty-one breast cancer (BC) patient-derived xenograft (PDX) models. Fourteen out of 31 (45%) PDXs exhibited a profound and sustained response to HER3-DXd. Basal-like PAM50 intrinsic subtype, limited prior exposure to chemotherapy and intrinsic sensitivity to the TOP1i irinotecan were associated with long-term response. Additionally, HER3-DXd showed sustained activity in BRCA1/BRCA2-mutated PARPi-resistant PDX models. Long-term responders exhibited persistent DNA damage and lacked early transcriptional activation of the G2/M cell cycle checkpoint that allow for DNA repair and RNA-DNA hybrid (R-loop) resolution, in parallel resulting in immune pathways transcriptional activation. Notably, characteristics linked to long-term response were primarily associated with the TOP1i payload activity.

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Publication Details

Journal
npj Precision Oncology
Published
2025-11-21
DOI
https://doi.org/10.1038/s41698-025-01172-5
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Determinants of long-term response to patritumab deruxtecan in breast cancer patient-derived xenografts

Olga Rodríguez, Fara Brasó‐Maristany, Anna Esteve‐Codina, Eloi Casals et al.
npj Precision Oncology
HER2/EGFR in Cancer Research
article

Determinants of long-term response to patritumab deruxtecan in breast cancer patient-derived xenografts

Olga Rodríguez, Fara Brasó‐Maristany, Anna Esteve‐Codina, Eloi Casals, Laia Monserrat, Judit Grueso, Flaminia Pedretti, Eduardo García‐Galea, Sarat Chandarlapaty, Cristina Molina, Pang‐Dian Fan, Fumitaka Suto, Andreu Òdena, Violeta Serra, Andrea Herencia-Ropero, Marta Guzmán, Rodrigo Dienstmann, Heura Domènech, Mafalda Oliveira, Aleix Prat
article en

Abstract

Novel antibody-drug conjugates (ADCs) have shown potent antitumor activity across multiple cancer types. However, the key determinants of therapeutic response remain under investigation. In this study, we aimed to identify potential determinants of long-term response to patritumab deruxtecan (HER3-DXd; MK-1022), a HER3-directed ADC linked to a potent topoisomerase I inhibitor (TOP1i) payload, using a cohort of thirty-one breast cancer (BC) patient-derived xenograft (PDX) models. Fourteen out of 31 (45%) PDXs exhibited a profound and sustained response to HER3-DXd. Basal-like PAM50 intrinsic subtype, limited prior exposure to chemotherapy and intrinsic sensitivity to the TOP1i irinotecan were associated with long-term response. Additionally, HER3-DXd showed sustained activity in BRCA1/BRCA2-mutated PARPi-resistant PDX models. Long-term responders exhibited persistent DNA damage and lacked early transcriptional activation of the G2/M cell cycle checkpoint that allow for DNA repair and RNA-DNA hybrid (R-loop) resolution, in parallel resulting in immune pathways transcriptional activation. Notably, characteristics linked to long-term response were primarily associated with the TOP1i payload activity.

npj Precision OncologyVol. 9(1)
Universitat de Vic - Universitat Central de Catalunya (ES), Universitat Autònoma de Barcelona (ES), Memorial Sloan Kettering Cancer Center (US), Instituto Oncológico Dr. Rosell (ES), Vall d'Hebron Institut de Recerca (ES), Hospital Quirónsalud Barcelona (ES), Hospital Clínic de Barcelona (ES), Vall d'Hebron Hospital Universitari (ES), Centro Nacional de Análisis Genómico (ES), Oryzon Genomics (Spain) (ES), Consorci Institut D'Investigacions Biomediques August Pi I Sunyer (ES), Daiichi Sankyo (United States) (US), Vall d'Hebron Institute of Oncology (ES), Universitat de Barcelona (ES)
Agencia Estatal de Investigación
Openalex Percentile: Top 51%
HER2/EGFR in Cancer Research
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