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

被引:62
作者
Singh, Anurag K. [1 ]
Guion, Peter [2 ]
Sears-Crouse, Nancy [2 ]
Ullman, Karen [2 ]
Smith, Sharon [2 ]
Albert, Paul S. [3 ]
Fichtinger, Gabor [4 ]
Choyke, Peter L. [5 ]
Xu, Sheng [6 ]
Kruecker, Jochen [6 ]
Wood, Bradford J. [7 ]
Krieger, Axel [8 ]
Ning, Holly [2 ]
机构
[1] Roswell Pk Canc Inst, Dept Radiat Med, Buffalo, NY 14263 USA
[2] NCI, Radiat Oncol Branch, Bethesda, MD 20892 USA
[3] NCI, Biometr Res Branch, Div Canc Treatment & Diag, Bethesda, MD 20892 USA
[4] Queens Univ, Sch Comp, Kingston, ON, Canada
[5] NCI, Mol Imaging Program, NIH, Bethesda, MD 20892 USA
[6] Philips Res N Amer, Briarcliff Manor, NY USA
[7] NIH, Dept Diagnost Radiol, Ctr Clin, Bethesda, MD 20892 USA
[8] Johns Hopkins Univ, Dept Mech Engn, Baltimore, MD 21218 USA
关键词
D O I
10.1186/1748-717X-2-36
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To assess the feasibility and early toxicity of selective, IMRT-based dose escalation (simultaneous integrated boost) to biopsy proven dominant intra-prostatic lesions visible on MRI. Methods: 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. Results: 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. Conclusion: 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.
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页数:6
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