Evidence map›Paper›PMID 41216206›Full record

ArticleAdvances in radiation oncology2025

Dose Intensification to the Dominant Intraprostatic Lesion During Prostate Stereotactic Body Radiation Therapy Delivered on a Magnetic Resonance Imaging Linear Accelerator: Feasibility and Early Clinical Outcomes.

Michael J Zelefsky, David Byun, Matthew Long, Gabriel Fuligni, Hesheng Wang, Siming Lu, Ting Chen, David Barbee

Abstract read
In one paragraph

Article in Advances in radiation oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Michael J ZelefskyDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
David ByunDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
Matthew LongDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
Gabriel FuligniDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
Hesheng WangDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
Siming LuDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
Ting ChenDepartment of Radiation Oncology, NYU Langone Health, New York, New York.
David BarbeeDepartment of Radiation Oncology, NYU Langone Health, New York, New York.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study aims to evaluate the feasibility of delivering escalated doses to the dominant intraprostatic lesion (DIL) as noted on T2-weighted magnetic resonance imaging and diffusion-weighted imaging while maintaining dose to the surrounding normal tissue structures within dose-volume constraints. Methods and Materials: A total of 50 consecutive patients were treated with prostate stereotactic body radiation therapy (SBRT), via a simultaneous integrated boost to the DIL, on a 1.5-Tesla magnetic resonance imaging linear accelerator platform. These patients were treated with SBRT to 40 Gy in 5 fractions every other day, and the DIL was simultaneously boosted to 45 Gy in 5 fractions. No patient was treated with androgen deprivation therapy. The normal tissue structures and the prostate and DIL were recontoured, and a postfraction plan was generated to retrospectively generate the doses delivered to the prostate and the DIL boost target for each of these 250 therapy sessions. Results: On postfraction dosimetric analysis, the median dose to 95% (D95) of the DIL was 45.3 Gy (initial plan: 45.9 Gy; Conclusions: With real-time adaptive planning on a magnetic resonance imaging linear accelerator, dose escalation was achieved in most cases with the intended doses without significantly compromising the dose-volume constraints of the surrounding normal tissue structures. These dosimetric findings were associated with an excellent tolerance profile at 12 months and a low incidence of urinary or rectal toxicity.

Identifiers

PMID41216206
PMCPMC12596952

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