Gynecologic cancer

Delivering a complete gynecologic cancer solution for you and your patients ​

Trust the experts with over 20 years of experience. 

Over 118,000 women are newly diagnosed with gynecologic cancer annually in the U.S.¹

NeoGenomics gynecologic cancer solution supports the care continuum with tests that detect genomic alterations relevant to diagnosis, therapy selection, prognosis, and clinical trial options With deep genomic expertise and a commitment to precision, NeoGenomics empowers clinicians to deliver more informed, targeted care for patients facing gynecologic cancers.

Featured gynecologic cancer solutions

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NTG-HCSX-02AX
NTG-OTPX-02CX
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Comprehensive HRD Testing for Informed Ovarian Cancer Treatment

Approximately one in two patients with advanced ovarian cancer are HRD-positive,2 making HRD testing a critical step in guiding personalized treatment. Despite global guidelines recommending BRCA and HRD testing, many eligible patients remain untested—limiting access to biomarker-driven therapies.3

PanTracer Tissue + HRD offers comprehensive genomic profiling (CGP) with integrated HRD assessment. Our advanced HRD assessment covers BRCA1/2 mutation status and tumor genomic instability status (GIS), including LOH, TAI, and LST, to guide personalized treatment decisions.

With real-time molecular insights, PanTracer Tissue + HRD supports more informed, precise, and effective treatment strategies across the ovarian cancer care continuum.

Additional tests for gynecologic cancer

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APH-HEOX-01AX
MOG-HPVX-01AZ
MOG-BMAP-03AX
APT-FORP-01AX
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FOLR1

FOLR1

Folate receptor alpha (FRα), also known as FOLR1, is an actionable biomarker expressed in approximately 90% of ovarian cancers 7and minimally in normal tissues—making it an ideal target for FOLR1-directed therapies. The FDA-approved FOLR1 IHC assay is designed to assess FRα expression in ovarian cancer tissue and guide treatment selection.

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FOLR1 IHC testing
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References

References

American Cancer Society. Cancer Facts & Figures 2025.  Atlanta: American Cancer Society; 2025. 

Nogueira Rodrigues A, Souto AKdBA, de Andrade DAP, et al. Homologous recombination deficiency test validation in patients with high-gradeadvanced ovarian cancer. Front Mol Biosci. 2025;12:1524594. doi:10.3389/fmolb.2025.1524594 

Bender S. Physician Gaps in Genetic Testing Knowledge May Impact Ovarian Cancer Care. Am J Manag Care. Published March 26, 2024. Available at:https://www.ajmc.com/view/physician-gaps-in-genetic-testing-knowledge-may-impact-ovarian-cancer-care. Accessed March 28, 2025. 

Moore DC, Guinigundo AS. The role of biomarkers in guiding clinical decision-making in oncology. J Adv Pract Oncol. 2023;14(3):241-248.doi:10.6004/jadpro.2023.14.3.17 

Helwick C. NCCN Clinical Practice Guidelines in Oncology: 2023 Updates. The ASCO Post. Published May 25, 2023. Accessed May 7, 2025.

Roche Diagnostics. Roche receives CE Mark for VENTANA FOLR1 (FOLR1-2.1) RxDx Assay as the first IHC-based companion diagnostic to identifyovarian cancer patients eligible for ELAHERE. Published November 18, 2024. Accessed April 11, 2025.https://diagnostics.roche.com/global/en/news-listing/2024/roche-receives-ce-mark-for-ventana-folr1--folr1-2-1--rxdx-assay-.html