TY - JOUR
T1 - Focal Prostate Stereotactic Body Radiation Therapy With Correlative Pathological and Radiographic-Based Treatment Planning
AU - Fredman, Elisha
AU - Traughber, Bryan
AU - Kharouta, Michael
AU - Podder, Tarun
AU - Lo, Simon
AU - Ponsky, Lee
AU - MacLennan, Gregory
AU - Paspulati, Raj
AU - Ellis, Bradley
AU - Machtay, Mitchell
AU - Ellis, Rodney
N1 - Funding Information:
This work was supported by Elekta, Stockholm, Sweden (monetary funding) and Philips, Andover, MA (provided the UroNav system for use) (grant numbers 16053.01.N0442 and 15976.01.L2397). The funders were not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication. Of the authors above, those directly impacted by these grants are RE, BT, and MM. There was also support from the Case Comprehensive Cancer Center Core grant (grant number 2P30CA043703-28). Part of this manuscript was presented as an abstract at the American Society for Radiation Oncology Annual Meeting, San Antonia TX, October 2018, and further findings were presented at the American Radium Society Annual Meeting, Dana Point CA, April 2019.
Funding Information:
We are grateful to the following people for their meaningful contributions to our tandem clinical trials: Aryavarta Kumar (aryavarta.kumar@va.gov; Division of Radiation Oncology, Louis Stokes Cleveland VA Medical Center, Cleveland, OH, USA), Liwei Jia (jial@mskcc.org; Department of Pathology, University Hospitals, Cleveland Medical Center, Cleveland, OH, USA), and Ethan Lemke (ethan.lemke@wartburg.edu; Wartburg College, Waverly, IA, USA).
Publisher Copyright:
© Copyright © 2021 Fredman, Traughber, Kharouta, Podder, Lo, Ponsky, MacLennan, Paspulati, Ellis, Machtay and Ellis.
PY - 2021/9/15
Y1 - 2021/9/15
N2 - Introduction: Advances in multiparametric MRI (mpMRI) combining anatomic and functional imaging can accurately identify foci of adenocarcinoma within the prostate, offering the possibility of partial gland therapy. We performed tandem prospective pilot trials to investigate the feasibility of focal prostate SBRT (f-SBRT) based on correlating diagnostic mpMRI and biopsies with confirmatory pathology in treatment planning. Materials and Methods: Patients with pathologic focal Gleason 6–7 disease and a corresponding PIRADS 4–5 lesion on mpMRI underwent targeted and comprehensive biopsies using MRI/ultrasound fusion under electromagnetic sensor navigation. After rigorous analysis for imaging biopsy concordance, five of 18 patients were eligible to proceed to f-SBRT. Chi-squared test was used for differences from expected outcomes, and concordance was estimated with binomial distribution theory and Wilson’s method. Results: Six patients had Gleason 6 and 12 had Gleason 3 + 4 disease (mean PSA: 5.8 ng/ml, range: 2.2–8.4). Absolute concordance was 43.8% (95% CI: 0.20, 0.64). Patterns of discordance included additional sites of ipsilateral disease, bilateral disease, and negative target. Five were upstaged to a new NCCN risk category necessitating treatment escalation. The five patients with concordant pathology completed three-fraction f-SBRT with sparing of the surrounding normal structures (including contralateral neurovascular bundle), with no reported grade 2+ toxicities and favorable PSA responses (mean: 41% decrease). Conclusions: On our pilot trials of f-SBRT planning using rigorous imaging and pathology concordance, image-guided confirmatory biopsies frequently revealed additional disease, suggesting the need for caution in partial-gland therapy. For truly focal disease, f-SBRT provided excellent dosimetry, minimal toxicity, and encouraging biochemical response. Clinical Trial Registration: www.clinicaltrials.gov, NCT02681614; NCT02163317.
AB - Introduction: Advances in multiparametric MRI (mpMRI) combining anatomic and functional imaging can accurately identify foci of adenocarcinoma within the prostate, offering the possibility of partial gland therapy. We performed tandem prospective pilot trials to investigate the feasibility of focal prostate SBRT (f-SBRT) based on correlating diagnostic mpMRI and biopsies with confirmatory pathology in treatment planning. Materials and Methods: Patients with pathologic focal Gleason 6–7 disease and a corresponding PIRADS 4–5 lesion on mpMRI underwent targeted and comprehensive biopsies using MRI/ultrasound fusion under electromagnetic sensor navigation. After rigorous analysis for imaging biopsy concordance, five of 18 patients were eligible to proceed to f-SBRT. Chi-squared test was used for differences from expected outcomes, and concordance was estimated with binomial distribution theory and Wilson’s method. Results: Six patients had Gleason 6 and 12 had Gleason 3 + 4 disease (mean PSA: 5.8 ng/ml, range: 2.2–8.4). Absolute concordance was 43.8% (95% CI: 0.20, 0.64). Patterns of discordance included additional sites of ipsilateral disease, bilateral disease, and negative target. Five were upstaged to a new NCCN risk category necessitating treatment escalation. The five patients with concordant pathology completed three-fraction f-SBRT with sparing of the surrounding normal structures (including contralateral neurovascular bundle), with no reported grade 2+ toxicities and favorable PSA responses (mean: 41% decrease). Conclusions: On our pilot trials of f-SBRT planning using rigorous imaging and pathology concordance, image-guided confirmatory biopsies frequently revealed additional disease, suggesting the need for caution in partial-gland therapy. For truly focal disease, f-SBRT provided excellent dosimetry, minimal toxicity, and encouraging biochemical response. Clinical Trial Registration: www.clinicaltrials.gov, NCT02681614; NCT02163317.
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U2 - 10.3389/fonc.2021.744130
DO - 10.3389/fonc.2021.744130
M3 - Article
C2 - 34604088
AN - SCOPUS:85116188196
SN - 2234-943X
VL - 11
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 744130
ER -