Pretargeted alpha therapy in MUC16-positive high-grade serous ovarian cancer

Peritoneal metastasis with micrometastatic cell clusters is a common feature of advanced ovarian cancer. Targeted alpha therapy (TAT) is an attractive approach for treating micrometastatic diseases as alpha particles release enormous amounts of energy within a short distance. A pretargeting approach...

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Veröffentlicht in:Nuclear medicine and biology 2025-01, Vol.140-141, p.108976, Article 108976
Hauptverfasser: Mack, Kyeara N., Bauer, David, Carter, Lukas M., Carrasco, Sebastian E., Atmane, Mohamed I., Viray, Tara D., Brooks, Cory L., Hollingsworth, Michael A., Radhakrishnan, Prakash, Lewis, Jason S.
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Sprache:eng
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Zusammenfassung:Peritoneal metastasis with micrometastatic cell clusters is a common feature of advanced ovarian cancer. Targeted alpha therapy (TAT) is an attractive approach for treating micrometastatic diseases as alpha particles release enormous amounts of energy within a short distance. A pretargeting approach — leveraging the inverse-electron-demand Diels-Alder reaction between tetrazines (Tz) and trans-cyclooctene (TCO) — can minimize off-target toxicity related to TAT, often associated with full-length antibodies. We hypothesized that a pretargeting strategy could effectively treat high-grade serous (HGS) ovarian tumors while minimizing toxicity. We utilized the humanized antibody, AR9.6, labeled with actinium-225 (225Ac). AR9.6 targets fully glycosylated and hypoglycosylated isoforms of MUC16. For biodistribution and radioimmunotherapy studies, AR9.6-TCO was injected into OVCAR3-bearing mice 72 h before administering [225Ac]Ac-mcp-PEG8-Tz, e.g. using a 1,2,4,5-tetrazine conjugated to the macropa chelator via a polyethylene glycol (PEG) linker. Biodistribution data revealed that the pretargeting approach achieved substantial tumor uptake. Cerenkov luminescence imaging confirmed successful in vivo pretargeting during TAT studies. Compared to the control groups, TAT with AR9.6-TCO and [225Ac]Ac-mcp-PEG8-Tz significantly suppressed tumor growth and improved overall survival in OVCAR3 tumor-bearing mice. Renal and ovarian pathology compatible with toxicity was observed in mice in addition to transient hematologic toxicity. We confirmed that pretargeting with AR9.6-TCO and [225Ac]Ac-mcp-PEG8-Tz has durable antitumor effects in high MUC16-expressing tumors. These findings demonstrate great potential for using pretargeting in combination with TAT for the treatment of ovarian cancer. Biological Sciences; Applied Biological Sciences. [Display omitted] •Ovarian cancer is a ‘silent killer’ since it is often diagnosed at advanced stages.•Patients are often diagnosed at a stage with peritoneal metastases — microscopic tumors that are challenging to treat.•Targeted alpha therapy (TAT) is a promising approach for treating micrometastatic lesions.•A pretargeting approach can mitigate off-target toxicities that often accompany full-length antibody based radioimmunotherapies.
ISSN:0969-8051
1872-9614
1872-9614
DOI:10.1016/j.nucmedbio.2024.108976