Objective: Therapeutic decision-making in metastatic renal cell carcinoma (MRCC) is based on conventional radiological evaluation. Fluorodeoxyglucose positron emission tomography (FDG-PET) scans may modify this strategy. Methods: Patients with MRCC for whom a therapeutic decision had been made underwent an FDG-PET scan in order to complete the standard radiological evaluation. Results: Twenty-four patients and 26 FDG-PET scans were eligible. In 18 patients, metastatic disease was evaluable on the computed tomography (CT) scan; the FDG-PET scan was positive in 16 patients and negative in 10. In 2 patients, the FDG-PET scan was positive while they were considered disease free on radiological evaluation. In 5 patients (20.8%), the previous therapeutic decision was changed. Thirteen patients had a pathological evaluation for 19 sites. One patient out of 13 had a false-positive FDG-PET scan, while 4 sites out of 6 were false-negative. The sensitivity was 75% (95% CI: 47.6–92.7) and the predictive positive value was 92.3% (95% CI: 64–99.8). With a median follow-up of 24 months, 3 patients developed new metastatic sites. Conclusion: Our data suggest that, when positive, an FDG-PET scan may modify the decision made; when negative, it should not modify decision-making especially for surgery, owing to its sensitivity.

1.
Linehan WM, Bates SE, Yang JC: Cancer of the kidney and ureter; in DeVita VT Jr, Helmann S, Rosenberg SA (eds): Cancer: Principles and Practice of Oncology, ed 7. Philadelphia, Lippincott Williams and Wilkins, 2004, pp 1139–1167.
2.
Motzer RJ, Bander NH, Nanus DM: Renal cell carcinoma. N Engl J Med1996;335:865–875.
3.
Ravaud A, Debled M: Present achievements in the medical treatment of metastatic renal cell carcinoma. Crit Rev Oncol Hematol 1999;31:77–87.
4.
Fyfe GA, Fisher RI, Rosenberg SA, Sznol M, Parkinson DR, Louie AC: Long-term response data for 255 patients with metastatic renal cell carcinoma treated with high-dose recombinant interleukin-2 therapy. J Clin Oncol 1996;14:2410–2411.
5.
Négrier S, Escudier B, Lasset C, Douillard JY, Savary J, Chevreau C, Ravaud A, Mercatello A, Peny J, Mousseau M, Philip T, Tursz T, Groupe Français d’Immunothérapie: Recombinant human interleukin-2, recombinant human interferon alfa-2a, or both in metastatic renal-cell carcinoma. N Engl J Med 1998;338:1272–1278.
6.
Tanguay S, Swanson DA, Putnam JB Jr: Renal cell carcinoma metastatic to the lung: potential benefit in the combination of biological therapy and surgery. J Urol 1996;156:1586–1589.
7.
Kavolius JP, Mastorakos DP, Pavlovich C, Russo P, Burt ME, Brady MS: Resection of metastatic renal cell carcinoma. J Clin Oncol 1998;1:2261–2266.
8.
Sella A, Swanson DA, Roy JY, Putnam JB Jr, Amato RJ, Markowitz AB, Logothetis CJ: Surgery following response to interferon-α-based therapy for residual renal cell carcinoma. J Urol 1993;149:19–21.
9.
Pogrebniak HW, Haas G, Linehan W, Rosenberg SA, Pass HI: Renal cell carcinoma: resection of solitary and multiple metastases. Ann Thorac Surg 1992;54:33–38.
10.
Ramdave S, Thomas GW, Berlangieri SU, Bolton DM, Davis I, Danguy HT, Macgregor D, Scott AM: Clinical role of F-18 fluorodeoxyglucose positron emission tomography for detection and management of renal cell carcinoma. J Urol 2001;166:825–830.
11.
Brouwers AH, Dorr U, Lang O, Boerman OC, Oyen WJ, Steffens MG, Oosterwijk E, Mergenthaler HG, Bihl H, Corstens FH: 131I-cG250 monoclonal antibody immunoscintigraphy versus [18F]FDG-PET imaging in patients with metastatic renal cell carcinoma: a comparative study. Nucl Med Commun 2002;23:229–236.
12.
Safaei A, Figlin R, Hoh CK, Silverman DH, Seltzer M, Phelps ME, Czernin J: The usefulness of F-18 deoxyglucose whole-body positron emission tomography (PET) for re-staging of renal cancer. Clin Nephrol 2002;57:56–62.
13.
Majhail NS, Urbain JL, Albani JM, Kanvinde MH, Rice TW, Novick AC, Mekhail TM, Olencki TE, Elson P, Bukowski RM: F-18 fluorodeoxyglucose of distant metastases from renal cell carcinoma. J Clin Oncol 2003;21:3995–4000.
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