Abstract A034: HIF-2-mediated gene expression is highest in metastatic and cluster-exclude clear cell renal cell carcinoma tumors

Abstract Introduction: Hypoxia inducible factor (HIF)-2 inhibitors are FDA-approved for the treatment of metastatic clear cell renal cell carcinoma (ccRCC). In theory, all ccRCC tumors should exhibit HIF-2 stabilization due to VHL silencing. However, many patients fail to respond to HIF-2 inhibitors. A biomarker to identify patients most likely to respond to HIF-2 inhibitors is needed. Methods: In this analysis, we explored a HIF-2 gene expression signature (Courtney et al., Clinical Cancer Research 2020) in two independent cohorts of patients with metastatic ccRCC. The two cohorts include a discovery multi-institutional cohort from VUMC, UTSW, and Rutgers that includes 205 tumor samples, including 12 matched primary:metastatic pairs. As a validation cohort, we utilized samples from the prospective phase 2 OPTIC RCC trial (NCT05361720), which includes 95 samples and 23 matched primary:metastatic pairs. Results: In the discovery cohort, the HIF-2 gene expression signature was higher in metastatic tumors than in primary tumors (p<0.01). Likewise, 75% of matched primary:metastatic pairs showed higher expression in the metastatic tumor (p<0.05). When examining the OPTIC RCC gene expression signatures, we observed higher levels of the HIF-2 gene expression signature in cluster_Exclude tumors compared with cluster_Angio or cluster_IO tumors (p<0.01). In the OPTIC RCC validation cohort, we observed similar trends, including higher expression of the HIF-2 gene expression signature in metastatic tumors from matched primary:metastatic pairs (p<0.05) and in cluster_Exclude relative to cluster_Angio tumors (p<0.01). We will also identify OPTIC RCC patients with high expression of the HIF-2 gene expression signature and assess their response to approved regimens for previously untreated ccRCC, including ipilimumab plus nivolumab and cabozantinib plus nivolumab. Conclusion: Metastatic tumors exhibit higher expression of a HIF-2 gene expression signature relative to primary tumors. In addition, the OPTIC RCC cluster_Exclude tumors have the highest levels of HIF-2 gene expression signatures, a group of tumors that have a poor overall prognosis. Citation Format: Scott M. Haake, Katy Beckermann, Alex Nesta, Eric Davis, Pedro C. Barata, Moshe C. Ornstein, Nataliya Mar, Ellen Heimann-Nichols, Tian Zhang, James Brugarolas, Anupama Reddy, Brian I. Rini. HIF-2-mediated gene expression is highest in metastatic and cluster-exclude clear cell renal cell carcinoma tumors [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Kidney Cancer Research: From Molecular Insights to Therapeutic Breakthroughs; 2026 Mar 13-16; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(5_Suppl_2):Abstract nr A034.

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Journal
Cancer Research
Published
2026-03-13
DOI
https://doi.org/10.1158/1538-7445.kidney26-a034
Primary Topic
Cancer, Hypoxia, and Metabolism
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article

Abstract A034: HIF-2-mediated gene expression is highest in metastatic and cluster-exclude clear cell renal cell carcinoma tumors

Scott M. Haake, Brian I. Rini, Anupama Reddy, James Brugarolas et al.
Cancer Research
Cancer, Hypoxia, and Metabolism
article

Abstract A034: HIF-2-mediated gene expression is highest in metastatic and cluster-exclude clear cell renal cell carcinoma tumors

Scott M. Haake, Brian I. Rini, Anupama Reddy, James Brugarolas, Ellen Heimann-Nichols, Alex Nesta, Katy Beckermann, Nataliya Mar, Pedro C. Barata, Tian Zhang, Moshe C. Ornstein, Eric Davis
article en

Abstract

Abstract Introduction: Hypoxia inducible factor (HIF)-2 inhibitors are FDA-approved for the treatment of metastatic clear cell renal cell carcinoma (ccRCC). In theory, all ccRCC tumors should exhibit HIF-2 stabilization due to VHL silencing. However, many patients fail to respond to HIF-2 inhibitors. A biomarker to identify patients most likely to respond to HIF-2 inhibitors is needed. Methods: In this analysis, we explored a HIF-2 gene expression signature (Courtney et al., Clinical Cancer Research 2020) in two independent cohorts of patients with metastatic ccRCC. The two cohorts include a discovery multi-institutional cohort from VUMC, UTSW, and Rutgers that includes 205 tumor samples, including 12 matched primary:metastatic pairs. As a validation cohort, we utilized samples from the prospective phase 2 OPTIC RCC trial (NCT05361720), which includes 95 samples and 23 matched primary:metastatic pairs. Results: In the discovery cohort, the HIF-2 gene expression signature was higher in metastatic tumors than in primary tumors (p<0.01). Likewise, 75% of matched primary:metastatic pairs showed higher expression in the metastatic tumor (p<0.05). When examining the OPTIC RCC gene expression signatures, we observed higher levels of the HIF-2 gene expression signature in cluster_Exclude tumors compared with cluster_Angio or cluster_IO tumors (p<0.01). In the OPTIC RCC validation cohort, we observed similar trends, including higher expression of the HIF-2 gene expression signature in metastatic tumors from matched primary:metastatic pairs (p<0.05) and in cluster_Exclude relative to cluster_Angio tumors (p<0.01). We will also identify OPTIC RCC patients with high expression of the HIF-2 gene expression signature and assess their response to approved regimens for previously untreated ccRCC, including ipilimumab plus nivolumab and cabozantinib plus nivolumab. Conclusion: Metastatic tumors exhibit higher expression of a HIF-2 gene expression signature relative to primary tumors. In addition, the OPTIC RCC cluster_Exclude tumors have the highest levels of HIF-2 gene expression signatures, a group of tumors that have a poor overall prognosis. Citation Format: Scott M. Haake, Katy Beckermann, Alex Nesta, Eric Davis, Pedro C. Barata, Moshe C. Ornstein, Nataliya Mar, Ellen Heimann-Nichols, Tian Zhang, James Brugarolas, Anupama Reddy, Brian I. Rini. HIF-2-mediated gene expression is highest in metastatic and cluster-exclude clear cell renal cell carcinoma tumors [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Kidney Cancer Research: From Molecular Insights to Therapeutic Breakthroughs; 2026 Mar 13-16; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(5_Suppl_2):Abstract nr A034.

Cancer ResearchVol. 86(5_Supplement_2)
Cleveland Clinic (US), University of California, Irvine (US), University Hospitals of Cleveland (US), North Carolina Institute of Medicine (US), Southwestern Medical Center (US), Tennessee Oncology (US), Irvine University (US), The University of Texas Southwestern Medical Center (US), Vanderbilt University Medical Center (US)
Good health and well-being
Openalex Percentile: Top 22%
Cancer, Hypoxia, and Metabolism
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