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Volume 59, Issue 2, Pages 419-425 (1 June 2004)


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Radioactive seed migration to the chest after transperineal interstitial prostate brachytherapy: extraprostatic seed placement correlates with migration

Originally presented at the 43rd Annual Meeting of the American Society for Therapeutic Radiology and Oncology, November 2001.

Jeffrey S Eshleman, M.D.*, Brian J Davis, M.D., Ph.D.*Corresponding Author Informationemail address, Thomas M Pisansky, M.D.*, Torrence M Wilson, M.D., Michael G Haddock, M.D.*, Bernard F King, M.D., Charles H Darby, M.S.§, Wayne N Lajoie, B.S.*, Ann L Oberg, Ph.D.§

Received 26 June 2003; accepted 15 October 2003.

Abstract 

Purpose

To examine the incidence of seed migration detected on chest X-ray and to identify the predictors associated with its occurrence.

Methods and materials

Between May 1998 and April 2000, 102 patients underwent permanent prostate brachytherapy at our institution and 100 were eligible for the study. Chest X-rays obtained at follow-up were examined for the number and location of seeds. The patient and treatment variables potentially associated with the occurrence and number of seed migrations were analyzed.

Results

One or more seeds were identified on the chest X-rays of 55 (55%) of 100 patients. The mean number of intrathoracic seeds in patients with migration was 2.2 (range, 1–10), and the proportion of seeds that migrated to the thorax was 0.98%. The rate of extraprostatic seeds planned was 43.9%, and postimplant CT identified 37.9% in such a location. The number of seeds planned for extraprostatic placement and below the apex were statistically significant (α = 0.05) predictors in univariate logistic analysis. Multivariate analysis revealed the planned number of extraprostatic seeds as the only statistically significant predictor (p = 0.04).

Conclusion

Extraprostatic placement of loose seeds is associated with an increased likelihood for, and frequency of, seed migration to the thorax. Nonetheless, the small proportion of implanted seeds that migrated (≤1%) is highly unlikely to have significant dosimetric consequences.

* Division of Radiation Oncology, Mayo Clinic, Rochester, MN, USA

 Department of Urology, Mayo Clinic, Rochester, MN, USA

 Department of Diagnostic Radiology, Mayo Clinic, Rochester, MN, USA

§ Division of Biostatistics, Mayo Clinic, Rochester, MN, USA

Corresponding Author InformationReprint requests to: Brian J. Davis, M.D., Ph.D., Division of Radiation Oncology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA. Tel: (507) 284-3191; Fax: (507) 284-0079

PII: S0360-3016(03)02286-7

doi:10.1016/j.ijrobp.2003.10.050


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