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Clinical Cancer Research Vol. 11, 3714-3721, May 15, 2005
© 2005 American Association for Cancer Research


Imaging, Diagnosis, Prognosis

Carbonic Anhydrase IX Expression Predicts Outcome of Interleukin 2 Therapy for Renal Cancer

Michael Atkins1,4, Meredith Regan2,4, David McDermott1,4, James Mier1,4, Eric Stanbridge5,6, Amanda Youmans1, Philip Febbo2,4, Melissa Upton1, Mirna Lechpammer2 and Sabina Signoretti2,4

Authors' Affiliations: 1 Division of Hematology/Oncology, Beth Israel Deaconess Medical Center; 2 Dana-Farber/Harvard Cancer Institute; 3 Brigham and Women's Hospital, Harvard Medical School; 4 Dana-Farber/Harvard Cancer Central Renal Cancer Program, Boston, MA; and Departments of 5 Microbiology and 6 Molecular Genetics, Irvine College of Medicine, University of California, Irvine, California

Requests for reprints: Michael B. Atkins, Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, MA 02215. Phone: 617-667-1930; Fax: 617-975-8030; E-mail: Matkins{at}bidmc.harvard.edu.

Purpose: Renal cancer response to interleukin 2 (IL-2) therapy and patient survival has been correlated with tumor histology and carbonic anhydrase IX (CAIX) expression. In an effort to confirm and expand these observations, we examined CAIX expression in pathology specimens from renal cancer patients who had previously received IL-2 therapy.

Experimental Design: Paraffin-embedded tissue sections of renal cancer were immunostained with the MN-75 monoclonal antibody to CAIX and expression levels were correlated with histologic findings and clinical outcome.

Results: Tissue specimens were obtained from 66 patients; 27 of whom (41%) had responded to IL-2–based therapy. Fifty-eight specimens were assessed as clear cell, with 56, 33, and 4 having alveolar, granular, and papillary features, respectively. Twenty-four (36%), 31 (47%), and 11 (17%) were classified into good, intermediate, and poor prognosis groups according to the Upton pathology model. Forty-one specimens (62%) had high CAIX expression. Twenty-one of 27 (78%) responding patients had high CAIX expressing tumors compared with 20 of 39 (51%) nonresponders (odds ratio, 3.3; P = 0.04). Median survival was prolonged (P = 0.04) and survival >5 years was only seen in high CAIX expressers. In patients with intermediate pathologic prognosis, all nine responders had high CAIX expression versus 11 of 22 nonresponders. A resultant group with good pathologic prognosis alone or with intermediate pathologic prognosis and high CAIX contained 26 of 27 (96%) responders compared with 18 of 39 (46%) nonresponders (odds ratio, 30; P < 0.01) and exhibited longer median survival (P < 0.01).

Conclusions: CAIX expression seems to be an important predictor of outcome in renal cell carcinoma patients receiving IL-2–based therapy and may enhance prognostic information obtained from pathology specimens.

Key Words: Renal cancer • Interleukin 2 • CAIX expression • histologic features




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 2005 by the American Association for Cancer Research.