1. Academic Validation
  2. Identification of CADM1 as an Immunotherapeutic Target and Evaluation of a Novel CADM1-Targeting Antibody-Drug Conjugate in Preclinical Osteosarcoma Models

Identification of CADM1 as an Immunotherapeutic Target and Evaluation of a Novel CADM1-Targeting Antibody-Drug Conjugate in Preclinical Osteosarcoma Models

  • Mol Cancer Ther. 2026 Jan 10:10.1158/1535-7163.MCT-25-0450. doi: 10.1158/1535-7163.MCT-25-0450.
Yifei Wang 1 Zhongting Zhang 1 Caterina Longo 2 Wendong Zhang 1 Qi Wang 1 Amer Najjar 2 Xiangjun Tian 3 Rossana N Lazcano Segura 2 Michael E Roth 1 Jonathan Gill 1 Douglas J Harrison 1 Zhaohui Xu 1 Yanhua Yi 4 Xin Zhou 1 Sylvester Jusu 1 Timothy M Stearns 5 Steven B Neuhauser 6 Carol J Bult 5 Jing Wang 7 Alexander J Lazar 1 Richard Gorlick 1
Affiliations

Affiliations

  • 1 The University of Texas MD Anderson Cancer Center Houston, TX United States.
  • 2 The University of Texas MD Anderson Cancer Center Houston United States.
  • 3 The University of Texas MD Anderson Cancer Center ´Houston, TX United States.
  • 4 The University of Texas MD Anderson Cancer Center Houston, Texas United States.
  • 5 Jackson Laboratory Bar Harbor, ME United States.
  • 6 Jackson Laboratory Bar Harbor, Maine United States.
  • 7 The University of Texas MD Anderson Cancer Center Houston,, Texas United States.
Abstract

Due to the paucity of validated cell surface osteosarcoma-specific targets, patients with this condition have long been excluded from the benefits of antibody-drug conjugate (ADC) therapy observed in patients with several solid and hematologic malignancies. Our comprehensive surfaceome profiling approach previously identified osteosarcoma-specific cell-surface antigens that are highly expressed in osteosarcomas but minimally expressed in normal tissues. As a result, one such antigen, CADM1, was selected for the generation of an ADC. We tested a CADM1-targeting ADC with a tesirine payload (SG3249) in vitro in osteosarcoma, rhabdomyosarcoma, and neuroblastoma patient-derived xenograft cell lines. In vivo, we tested six CADM1-expressing osteosarcoma patient-derived xenograft models. The CADM1 ADC demonstrated significant antitumor activity in vitro across the osteosarcoma, rhabdomyosarcoma, and neuroblastoma cell lines. Additionally, it effectively reduced tumor volume and extended event-free survival in all six osteosarcoma PDX models tested. Notably, the CADM1 ADC achieved a major complete response in one model (OS2), complete responses in two models (OS1 and OS33), and partial responses in three models (OS9, OS17, and OS31). Based on these results, clinical development of CADM1-targeted therapies for osteosarcoma and Other CADM1-expressing pediatric solid tumors may be warranted.

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