Evidence map›Paper›PMID 40607005›Full record

ArticleClinical and translational radiation oncology2025

Urethral and bladder dosimetry and urinary toxicity in prostate cancer patients undergoing SBRT with and without intra-prostatic boost.

Nisha Bhargava, Martina Hurwitz, Josephine Levey, Lily Bennett, Joseph A Aronovitz, Daniel R Schmidt, Jonathan W Lischalk, Irving D Kaplan, Nima Aghdam

Abstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Nisha BhargavaDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center Boston, MA, USA.
Martina HurwitzDepartment of Radiation Oncology Brigham and Women's Hospital at Boston, Weymouth MA USA.
Josephine LeveyDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center Boston, MA, USA.
Lily BennettDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center Boston, MA, USA.
Joseph A AronovitzDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center Boston, MA, USA.
Daniel R SchmidtDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center Boston, MA, USA.
Jonathan W LischalkDepartment of Radiation Medicine, MedStar-Georgetown University Hospital, Washington, DC, USA.
Irving D KaplanDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center Boston, MA, USA.
Nima AghdamDepartment of Radiation Oncology, Perlmutter Cancer Center at New York University Langone Hospital-Long Island, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: To evaluate the dosimetric and toxicity profiles of stereotactic body radiotherapy (SBRT) for prostate cancer, comparing cohorts with and without intraprostatic boost (IPB) to assess feasibility and safety of IPB, with particular attention to urethral and bladder dose and toxicity. Materials and methods: This retrospective cohort study analyzed 349 patients with localized prostate cancer treated between 2018 and 2023. Of these, 266 received SBRT with IPB, and 83 received SBRT without IPB. Patients were treated using a robotic SBRT platform with fiducial tracking. Dosimetric parameters for the urethra, including D0.03cc, D0.3cc, and V40Gy, and for the bladder, including D0.03cc, D5cc, D10cc, and V37Gy, were evaluated. Acute and late toxicities were assessed using CTCAE criteria. Results: For the urethra, median values for D0.03cc, D0.3cc, and V40Gy, and for the bladder, median values D0.03cc, D5cc, D10cc, and V37Gy were compared and no statistically significant differences were observed between the two cohorts. Late urinary toxicity of grade 3 or higher occurred in 2.25 % of patients in the IPB group and 2.47 % in the no IPB group, with no grade 3 acute toxicities reported. Discussion: These findings support the use of SBRT using an IPB as a feasible and safe approach to achieve focal dose escalation to dominant intra-prostatic lesions (DILs) without significantly increasing urethra or bladder dose or toxicity. Future research should focus on standardizing DIL contouring, exploring adaptive planning techniques to increase accuracy, and prospectively studying toxicity and quality of life in patients treated with IPB with SBRT.

Indexed as

Dominant intraprostatic lesionFocal dose escalationProstatic neoplasmsStereotactic body radiation therapyUrethral dose constraintUrinary toxicity

Identifiers

PMID40607005
PMCPMC12209893

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