A humanized anaplastic lymphoma kinase (ALK)-directed antibody-drug conjugate with pyrrolobenzodiazepine payload demonstrates efficacy in ALK-expressing cancers

The Anaplastic Lymphoma Kinase (ALK) gene is a receptor tyrosine kinase (RTK) with expression restricted to the developing nervous system. Most neuroblastomas express native ALK protein on the cell surface and ALK is uniformly overexpressed in fusion-positive rhabdomyosarcoma and in subsets of metastatic colorectal carcinoma, melanoma, ovarian carcinoma, and breast carcinoma. Here, we first confirm that ALK RNA, protein, and tumor cell surface expression is elevated in multiple pediatric and adult malignancies with minimal expression in childhood normal tissues. We then demonstrate that a humanized ALK-directed antibody conjugated to pyrrolobenzodiazepine (CDX0239-PBD) is internalized in ALK-expressing neuroblastoma cell lines with cell surface expression-dependent cytotoxicity. Finally, we show that CDX0239-PBD exhibits potent antitumor efficacy including maintained complete responses in ALK-expressing patient and cell line-derived neuroblastoma, fusion-positive rhabdomyosarcoma, and colorectal carcinoma xenograft models. These data support the clinical development of a first-in-class ALK-directed antibody-drug conjugate (ADC) for multiple pediatric and adult ALK-expressing malignancies.

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Publication Details

Journal
Nature Communications
Published
2025-08-15
DOI
https://doi.org/10.1038/s41467-025-62979-1
Citations
3
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
4.17

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A humanized anaplastic lymphoma kinase (ALK)-directed antibody-drug conjugate with pyrrolobenzodiazepine payload demonstrates efficacy in ALK-expressing cancers

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3 citations
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article

A humanized anaplastic lymphoma kinase (ALK)-directed antibody-drug conjugate with pyrrolobenzodiazepine payload demonstrates efficacy in ALK-expressing cancers

David Groff, John M. Maris, Mark Gerelus, Smita Matkar, Cynthia Adams, Yimei Li, Kristopher R. Bosse, Jennifer Pogoriler, Dontcho V. Jelev, Adam J. Wolpaw, Diego Alvarado, Yaël P. Mossé, Timothy T. Spear, Gabriela M. Witek, Alberto D. Guerra, Martina Mazzeschi, Christina Acholla, Kateryna Krytska, Joshua R. Kalna, Colleen E. Casey, Skye Balyasny, Mustafa Mir, Mattia Lauriola, Dimiter S. Dimitrov, Paul Kamitsuka, Chuan Chen, Daniel Martı́nez, Khushbu Patel, Grant Li, Amber K Hamilton, Grace Polkosnik, Piotr Jung, Apratim Mukherje
article en
3 citations

Abstract

The Anaplastic Lymphoma Kinase (ALK) gene is a receptor tyrosine kinase (RTK) with expression restricted to the developing nervous system. Most neuroblastomas express native ALK protein on the cell surface and ALK is uniformly overexpressed in fusion-positive rhabdomyosarcoma and in subsets of metastatic colorectal carcinoma, melanoma, ovarian carcinoma, and breast carcinoma. Here, we first confirm that ALK RNA, protein, and tumor cell surface expression is elevated in multiple pediatric and adult malignancies with minimal expression in childhood normal tissues. We then demonstrate that a humanized ALK-directed antibody conjugated to pyrrolobenzodiazepine (CDX0239-PBD) is internalized in ALK-expressing neuroblastoma cell lines with cell surface expression-dependent cytotoxicity. Finally, we show that CDX0239-PBD exhibits potent antitumor efficacy including maintained complete responses in ALK-expressing patient and cell line-derived neuroblastoma, fusion-positive rhabdomyosarcoma, and colorectal carcinoma xenograft models. These data support the clinical development of a first-in-class ALK-directed antibody-drug conjugate (ADC) for multiple pediatric and adult ALK-expressing malignancies.

Nature CommunicationsVol. 16(1)
Children's Hospital of Philadelphia (US), Azienda USL di Bologna (IT), University of Pittsburgh Medical Center (US), Celldex Therapeutics (United States) (US), University of Pennsylvania (US), University of Bologna (IT)
U.S. Department of Defense, Howard Hughes Medical Institute, Hope Foundation, National Institutes of Health, National Cancer Institute
Openalex Percentile: Top 6%
Neuroblastoma Research and Treatments
4.17
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