Evidence map›Paper›PMID 40998272›Full record

ArticleInternational journal of radiation oncology, biology, physics2026

The Comparative Toxicity of Focal Ablation Versus Intensity Modulated Radiation Therapy for Prostate Cancer.

James B Yu, David M DeStephano, Brian Jeffers, Alexander E Tward, Catherine S Spina, David P Horowitz, Tony J C Wang, Lisa A Kachnic, Pamela R Soulos, Cary P Gross and 1 more

Abstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2026. 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

11 authors.

James B YuDepartment of Radiation Oncology, Dartmouth Cancer Center, 1 Medical Center Dr., Lebanon, New Hampshire; Cancer Outcomes, Public Policy, and Effectiveness Research (COPPER) Center at Yale, New Haven, Connecticut. Electronic address: james.b.yu@dartmouth.edu.
David M DeStephanoDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Brian JeffersDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Alexander E TwardDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Catherine S SpinaDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
David P HorowitzDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Tony J C WangDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Lisa A KachnicDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York.
Pamela R SoulosCancer Outcomes, Public Policy, and Effectiveness Research (COPPER) Center at Yale, New Haven, Connecticut.
Cary P GrossCancer Outcomes, Public Policy, and Effectiveness Research (COPPER) Center at Yale, New Haven, Connecticut; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Simon K ChengDepartment of Radiation Oncology, Columbia University Irving Medical Center, New York, New York; Radiation Oncology Service, James J. Peters Veteran Affairs Medical Center, Bronx, New York.

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
NCI NIH HHS P30 CA013696NCI NIH HHS P30 CA023108
6 · The paper itself

Abstract

purposeFocal ablative therapy (FT) aims to treat prostate cancer (PCa) with reduced toxicity compared with standard radiation therapy. There is an absence of studies comparing FT and intensity modulated radiation therapy (IMRT) for PCa. METHODS AND MATERIALS: Using the SEER-Medicare database, we identified fee-for-service Medicare beneficiaries with PCa diagnosed from 2010 to 2017. Patients who underwent IMRT were Mahalanobis matched 2:1 to FT patients based on demographics, Medicaid eligibility, comorbidity, flu vaccination, primary care access, year, cancer characteristics, and androgen-deprivation therapy. We used logistic regression models to assess the relation between treatment modality and the presence of claims indicative of a gastrointestinal or genitourinary complication within 6, 12, and 24 months of treatment.

resultsWe identified 9928 IMRT and 800 FT patients. After matching, patients treated with FT were less likely to have gastrointestinal toxicity (6.2%) within 12 months compared with IMRT patients (9.5%, odds ratio [OR]; 0.63 [95% CI, 0.45-0.88]); results were similar at 24 months (11.0% FT vs 21.5% for IMRT; OR, 0.45 [95% CI, 0.35-0.58]). Most gastrointestinal toxicity was because of diagnoses of rectal bleeding and colitis. In contrast, there were more claims indicative of genitourinary toxicity for FT compared with IMRT during the 0 to 12 (34.6% vs 15.8%; OR, 2.69 [95% CI, 2.21-3.28]) and 0 to 24 (41.7% vs 29.3%; OR, 1.69 [95% CI, 1.42-2.01]) month periods. The largest difference was in incontinence therapy (17.4% vs 7.5%, P < .01) and erectile dysfunction (18.2% vs 13.1%, P < .01), favoring IMRT.

conclusionsAmong older patients with PCa, FT was associated with a higher risk of incontinence and impotence, than IMRT. There was more colitis and rectal bleeding with IMRT versus FT, but related procedures were rare and not significantly different.

Identifiers

PMID40998272
PMCPMC13104316

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.