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Imaging, Diagnosis, Prognosis |
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-2based 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-2based therapy and may enhance prognostic information obtained from pathology specimens.
Key Words: Renal cancer Interleukin 2 CAIX expression histologic features
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