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m276-SL-PBD eradicates tumors and instigates long-lasting tumor-free survival in Merkel cell carcinoma preclinical models

  1. Author:
    Kunika, Mikaela D
    Kannan, Aarthi
    Velasco, Graham J
    Feng,Yang
    Seaman,Steven
    Das, Bhaba K
    Pham, Dillon
    Lambrecht, Nils
    Zhao, Haibo
    St Croix,Bradley
    Gao, Ling
  2. Author Address

    Southern California Institute for Research and Education, Long Beach, CA 90822, USA., Department of Dermatology, University of California-Irvine, Irvine, CA 92697, USA., Pathology Department, Tibor Rubin VA Medical Center, VA Long Beach Healthcare System, Long Beach, CA 90822, USA., Tumor Angiogenesis Unit, Mouse Cancer Genetics Program (MCGP), National Cancer Institute (NCI), NIH, Frederick, MD 21702, USA., Dermatology Section, Tibor Rubin VA Medical Center, VA Long Beach Healthcare System, Long Beach, CA 90822, USA.,
    1. Year: 2025
    2. Date: May 16
    3. Epub Date: 2025 04 15
  1. Journal: iScience
    1. 28
    2. 5
    3. Pages: 112436
  2. Type of Article: Article
  3. Article Number: 112436
  1. Abstract:

    Merkel cell carcinoma (MCC) is a rare but aggressive neuroendocrine carcinoma, and immune checkpoint inhibitors (ICIs) are the only approved therapy; nonetheless, resistance is notable and there is a critical need for novel effective therapies. Recently, CD276 was identified as a promising therapeutic target in human cancers. In preclinical studies, a modified CD276 antibody-drug conjugate (ADC) with pyrrolobenzodiazepine (m276-SL-PBD) elicited more potent anti-tumor effects than two CD276 ADCs currently in clinical trials. Here, we uncover notable CD276 expression in MCC patient tumors, and demonstrate m276-SL-PBD efficacy against MCC preclinical models. Complete eradication is observed in all xenografts bearing CD276 expression, with 82% achieving 180-day tumor-free survival after 4 or 5 weekly doses, and m276-SL-PBD remained efficacious against relapsed tumors. Of clinical relevance, m276-SL-PBD retains its potency in MCC-bearing humanized mice. Importantly, no detectable adverse effects were observed. Thus, m276-SL-PBD is a promising therapy for patients unsuitable or resistant to ICIs. © 2025 The Authors.

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External Sources

  1. DOI: 10.1016/j.isci.2025.112436
  2. PMID: 40384933
  3. PMCID: PMC12084002
  4. PII : S2589-0042(25)00697-2

Library Notes

  1. Fiscal Year: FY2024-2025
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