Volume 123, Issue 7 pp. 1699-1703
Cancer Therapy

Rationale for folate receptor alpha targeted therapy in “high risk” endometrial carcinomas

Monica Brown Jones

Corresponding Author

Monica Brown Jones

Department of Obstetrics and Gynecology, Division of Gynecologic Surgery, Mayo Clinic, Rochester, MN

Department of Experimental Pathology, Mayo Clinic, Rochester, MN

Fax: +507-266-9300.

Department of Gynecologic Surgery, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USASearch for more papers by this author
Christina Neuper

Christina Neuper

Department of Experimental Pathology, Mayo Clinic, Rochester, MN

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Amy Clayton

Amy Clayton

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN

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Andrea Mariani

Andrea Mariani

Department of Obstetrics and Gynecology, Division of Gynecologic Surgery, Mayo Clinic, Rochester, MN

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Gottfried Konecny

Gottfried Konecny

Department of Obstetrics and Gynecology, Division of Gynecologic Surgery, Mayo Clinic, Rochester, MN

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M. Bijoy Thomas

M. Bijoy Thomas

Department of Obstetrics and Gynecology, Division of Gynecologic Surgery, Mayo Clinic, Rochester, MN

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Gary Keeney

Gary Keeney

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN

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Lynn Hartmann

Lynn Hartmann

Department of Medical Oncology, Mayo Clinic, Rochester, MN

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Karl C. Podratz

Karl C. Podratz

Department of Obstetrics and Gynecology, Division of Gynecologic Surgery, Mayo Clinic, Rochester, MN

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First published: 21 July 2008
Citations: 46

Abstract

Advanced and recurrent endometrial cancers account for the majority of deaths from this disease with limited therapeutic options. High grade, and nonendometrioid histology, pathologically characterize the endometrial tumors associated with adverse outcome and are classified as “high risk”. The identification of molecular prognostic factors that might be targeted for therapy among “high risk” endometrial cancers is an active area of investigation. We hypothesize that the FRα, highly expressed in endometrial cancer cells, is a potential target for this disease. Our objectives were to determine if FRα overexpression is associated with adverse prognostic factors and worse outcome. Three hundred and thirty-two endometrial cancer cores were arrayed onto a tissue microarray and stained using a FRα-specific monoclonal antibody. Staining was scored as absent or weak and moderate or strong. Forty-one percent of 310 evaluable cases stained moderate/strong. Moderate/strong FRα staining was significantly associated with other poor prognostic factors including: advanced stage, nonendometrioid histology and high grade. An association was observed between moderate/strong FRα staining and recurrence (p < 0.0014). These findings support further exploring a role for FRα targeted approaches for therapy and diagnostics in endometrial cancer. © 2008 Wiley-Liss, Inc.

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