Volume 71, Issue 2 , Pages 358-361, 1 June 2008
Use of Local 111In-Capromab Pendetide Scan Results to Predict Outcome After Salvage Radiotherapy for Prostate Cancer
Purpose
The 111In-capromab pendetide scan (ProstaScint; Cytogen Corp., Princeton NJ) is approved by the Food and Drug Administration to evaluate increasing prostate-specific antigen (PSA) levels after radical prostatectomy. This study evaluated the role of prostate bed 111In-capromab pendetide scan findings to predict response to salvage radiotherapy (RT).
Methods and Materials
Forty patients who had PSA recurrence after radical prostatectomy and a 111In-capromab pendetide scan immediately before salvage prostate bed RT (median, 66 Gy) were identified from the Duke Prostate Center database. Patients with distant uptake of capromab pendetide or long-term androgen deprivation therapy were excluded. Median follow-up after salvage RT was 2.7 years. Patient demographic, clinical, and pathologic characteristics; PSA values; and 111In-capromab pendetide scan results were retrospectively analyzed. A PSA failure after salvage RT was defined as PSA level greater than 0.2 ng/ml. Data were combined with other published results in a secondary pooled analysis of 106 patients.
Results
111In-Capromab pendetide findings included 20 patients with negative scan results and 20 with locally positive scan results. Two-year progression-free survival rates were 60% for patients with a negative scan result and 74% for those with a locally positive scan result (p = 0.49). Combined analysis did not show a difference in outcome based on local 111In-capromab pendetide scan result.
Conclusion
For patients without distant signal detected by using 111In-capromab pendetide scan, patients with locally positive scan findings did not have statistically different progression-free survival than those with a negative scan result, suggesting that salvage RT may be successful in patients with either a locally positive or negative 111In-capromab pendetide scan result.
Capromab pendetide, ProstaScint, Adjuvant, Salvage, Radiotherapy
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Presented in part at the 2007 American Society of Clinical Oncology Prostate Symposium, February 22–24, 2007, Orlando, FL.
Conflict of interest: T.J. Polascik is a funded investigator for Cytogen Corp. J.Moul is a paid lecturer and consultant for Cytogen.
PII: S0360-3016(07)04443-4
doi:10.1016/j.ijrobp.2007.10.020
© 2008 Elsevier Inc. All rights reserved.
Volume 71, Issue 2 , Pages 358-361, 1 June 2008
