%0 Journal Article
%T Simultaneous integrated boost of biopsy proven, MRI defined dominant intra-prostatic lesions to 95 Gray with IMRT: early results of a phase I NCI study
%A Anurag K Singh
%A Peter Guion
%A Nancy Sears-Crouse
%A Karen Ullman
%A Sharon Smith
%A Paul S Albert
%A Gabor Fichtinger
%A Peter L Choyke
%A Sheng Xu
%A Jochen Kruecker
%A Bradford J Wood
%A Axel Krieger
%A Holly Ning
%J Radiation Oncology
%D 2007
%I BioMed Central
%R 10.1186/1748-717x-2-36
%X Patients with localized prostate cancer and an abnormality within the prostate on endorectal coil MRI were eligible. All patients underwent a MRI-guided transrectal biopsy at the location of the MRI abnormality. Gold fiducial markers were also placed. Several days later patients underwent another MRI scan for fusion with the treatment planning CT scan. This fused MRI scan was used to delineate the region of the biopsy proven intra-prostatic lesion. A 3 mm expansion was performed on the intra-prostatic lesions, defined as a separate volume within the prostate. The lesion + 3 mm and the remainder of the prostate + 7 mm received 94.5/75.6 Gray (Gy) respectively in 42 fractions. Daily seed position was verified to be within 3 mm.Three patients were treated. Follow-up was 18, 6, and 3 months respectively. Two patients had a single intra-prostatic lesion. One patient had 2 intra-prostatic lesions. All four intra-prostatic lesions, with margin, were successfully targeted and treated to 94.5 Gy. Two patients experienced acute RTOG grade 2 genitourinary (GU) toxicity. One had grade 1 gastrointestinal (GI) toxicity. All symptoms completely resolved by 3 months. One patient had no acute toxicity.These early results demonstrate the feasibility of using IMRT for simultaneous integrated boost to biopsy proven dominant intra-prostatic lesions visible on MRI. The treatment was well tolerated.There are over 200,000 new cases and nearly 30,000 deaths each year from prostate cancer [1]. Radiation therapy (RT) is a mainstay of local therapy. It has been established that biochemical disease free survival improves with dose escalation to the prostate[2-5]. However, growing evidence indicates that normal tissue complications also increase with increasing dose[4,6,7].The dosimetric parameters which correlate with late toxicity are being elucidated[2,7]. Advances in methods of precise radiation dose delivery, such as 3-dimensional conformal radiation therapy and intensity modulated RT (IMRT
%U http://www.ro-journal.com/content/2/1/36