Abstract 5697: EZH2 inhibition upregulates GD2 to enhance anti-GD2 immunotherapy in Ewing sarcoma

Abstract Introduction: Ewing sarcoma (ES) is a rare and aggressive malignancy of the bones and soft tissue for which substantial improvements in treatment options are desperately needed. ES cells heterogeneously express GD2, a surface marker for which there are targeted immunotherapies that are effective in other pediatric malignancies. The use of EZH2 inhibitors has been reported to increase expression of GD2 on the surface of sarcoma tumor cells. This study investigated the in vitro efficacy of an EZH2 inhibitor at increasing GD2 expression on ES cells with the aim of sensitizing them to anti-GD2 antibody treatment. Methods: Both commercial and patient derived ES cell lines were treated with low dose tazemetostat for an extended period, up to 28 days, followed by a withdrawal from treatment for 7 days. GD2 expression, cell cycle, and markers of apoptosis were evaluated at regular timepoints using a novel mass cytometry panel (CyTOF). OMIQ was used for data analysis and visualization. Efficacy of naxitamab was examined using immune cell killing assays on an Incucyte S3. Results: Tazemetostat treatment was found to increase GD2 expression on ES cells without significant impact on cell cycle or apoptosis. Elevation of GD2 expression was reversed upon withdrawal of drug. The addition of naxitamab displayed increased NK cell-mediated cell death in ES cells in response to increased GD2 expression. When pretreated with tazemetostat, GD2-low cell lines exhibit higher levels of apoptosis after treatment with naxitamab compared to untreated cells. Conclusions: This data supports the use of the EZH2 inhibitor tazemetostat for ES tumors that express low or heterogeneous levels of GD2 to enhance the effectiveness of GD2-targeting immunotherapeutic approaches. This study demonstrates the capability of CyTOF to look at multiple markers simultaneously to achieve a comprehensive characterization of various samples. Citation Format: Kenzie Wells, Kimberly Q. McKinney, Kaitlyn H. Smith, Poornima Gourabathini, Jeffrey Huo, Erin M. Trovillion, Javier Oesterheld, . EZH2 inhibition upregulates GD2 to enhance anti-GD2 immunotherapy in Ewing sarcoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5697.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-5697
Primary Topic
Neuroblastoma Research and Treatments
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article
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article

Abstract 5697: EZH2 inhibition upregulates GD2 to enhance anti-GD2 immunotherapy in Ewing sarcoma

Kimberly Q. McKinney, Jeffrey S. Huo, Poornima Gourabathini, Javier Oesterheld et al.
Cancer Research
Neuroblastoma Research and Treatments
article

Abstract 5697: EZH2 inhibition upregulates GD2 to enhance anti-GD2 immunotherapy in Ewing sarcoma

Kimberly Q. McKinney, Jeffrey S. Huo, Poornima Gourabathini, Javier Oesterheld, Erin Trovillion, Kenzie Wells
article en

Abstract

Abstract Introduction: Ewing sarcoma (ES) is a rare and aggressive malignancy of the bones and soft tissue for which substantial improvements in treatment options are desperately needed. ES cells heterogeneously express GD2, a surface marker for which there are targeted immunotherapies that are effective in other pediatric malignancies. The use of EZH2 inhibitors has been reported to increase expression of GD2 on the surface of sarcoma tumor cells. This study investigated the in vitro efficacy of an EZH2 inhibitor at increasing GD2 expression on ES cells with the aim of sensitizing them to anti-GD2 antibody treatment. Methods: Both commercial and patient derived ES cell lines were treated with low dose tazemetostat for an extended period, up to 28 days, followed by a withdrawal from treatment for 7 days. GD2 expression, cell cycle, and markers of apoptosis were evaluated at regular timepoints using a novel mass cytometry panel (CyTOF). OMIQ was used for data analysis and visualization. Efficacy of naxitamab was examined using immune cell killing assays on an Incucyte S3. Results: Tazemetostat treatment was found to increase GD2 expression on ES cells without significant impact on cell cycle or apoptosis. Elevation of GD2 expression was reversed upon withdrawal of drug. The addition of naxitamab displayed increased NK cell-mediated cell death in ES cells in response to increased GD2 expression. When pretreated with tazemetostat, GD2-low cell lines exhibit higher levels of apoptosis after treatment with naxitamab compared to untreated cells. Conclusions: This data supports the use of the EZH2 inhibitor tazemetostat for ES tumors that express low or heterogeneous levels of GD2 to enhance the effectiveness of GD2-targeting immunotherapeutic approaches. This study demonstrates the capability of CyTOF to look at multiple markers simultaneously to achieve a comprehensive characterization of various samples. Citation Format: Kenzie Wells, Kimberly Q. McKinney, Kaitlyn H. Smith, Poornima Gourabathini, Jeffrey Huo, Erin M. Trovillion, Javier Oesterheld, . EZH2 inhibition upregulates GD2 to enhance anti-GD2 immunotherapy in Ewing sarcoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5697.

Cancer ResearchVol. 86(7_Supplement)
Atrium Health Wake Forest Baptist (US), Wake Forest Baptist Comprehensive Cancer Center
Good health and well-being
Openalex Percentile: Top 14%
Neuroblastoma Research and Treatments
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