Evidence map›Paper›PMID 34585025›Full record

ArticleAdvances in radiation oncology

Toxicity After Stereotactic Body Radiation Therapy for Prostate Cancer in Patients With Inflammatory Bowel Disease: A Multi-institutional Matched Case-Control Series.

Jesus E Juarez, Tahmineh Romero, Constantine A Mantz, Abigail Pepin, Nima Aghdam, Simeng Suy, Michael L Steinberg, Rebecca G Levin-Epstein, Nicholas G Nickols, Irving D Kaplan and 11 more

Abstract read
In one paragraph

Article in Advances in radiation oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
–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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Review
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

21 authors.

Jesus E JuarezDepartment of Radiation Oncology, UCLA Medical Center, Los Angeles, California.
Tahmineh RomeroDepartment of Medicine Statistics Core, David Geffen School of Medicine at UCLA, Los Angeles, California.
Constantine A Mantz21st Century Oncology, Inc, Fort Meyers, Florida.
Abigail PepinDepartment of Radiation Medicine, Georgetown University Hospital, Washington, DC.
Nima AghdamDepartment of Radiation Medicine, Georgetown University Hospital, Washington, DC.
Simeng SuyDepartment of Radiation Medicine, Georgetown University Hospital, Washington, DC.
Michael L SteinbergDepartment of Radiation Oncology, UCLA Medical Center, Los Angeles, California.
Rebecca G Levin-EpsteinDepartment of Radiation Oncology, UCLA Medical Center, Los Angeles, California.
Nicholas G NickolsDepartment of Radiation Oncology, UCLA Medical Center, Los Angeles, California.
Irving D KaplanDepartment of Radiation Oncology, Beth Israel Deaconess, Boston, Massachusetts.
Robert M MeierSwedish Radiosurgery Center, Seattle, Washington.
Huong T PhamSection of Radiation Oncology, Virginia Mason Medical Center, Seattle, Washington.
Patrick W LinsonDepartment of Radiation Oncology, Scripps MD Anderson Cancer Center, San Diego, California.
Robert L HongDepartment of Radiation Oncology, Virginia Hospital Center, Arlington, Virginia.
Mark K BuyyounouskiDepartment of Radiation Oncology, Stanford University, Stanford, California.
Hilary P BagshawDepartment of Radiation Oncology, Stanford University, Stanford, California.
Donald B FullerDivision of Genesis Health care Partners Inc, CyberKnife Centers of San Diego Inc, San Diego, California.
Alan J KatzFlushing Radiation Oncology Services, New York.
Andrew LoblawDepartment of Radiation Oncology, Odette Cancer Center, Sunnybrook Health Sciences Center, Toronto, Ontario, Canada.
Sean P CollinsDepartment of Radiation Medicine, Georgetown University Hospital, Washington, DC.
Amar U KishanDepartment of Radiation Oncology, UCLA Medical Center, Los Angeles, California.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate the safety of stereotactic body radiation therapy (SBRT) for prostate cancer in men with inflammatory bowel disease (IBD). METHODS AND MATERIALS: We queried a consortium database for patients with IBD receiving SBRT for prostate cancer between 2006 and 2012. Identified patients were matched with patients without a history of IBD in a 3:1 fashion based on dose, fractionation, use of androgen deprivation therapy, and age distribution. Logistic regression was used to evaluate the association between having IBD and experiencing acute and late gastrointestinal (GI) and genitourinary (GU) toxicities as scored on the Common Terminology Criteria for Adverse Events scale. Time to late toxicity was evaluated using proportional hazard Cox models. Our study was limited by absence of data on prostate size, baseline International Prostate Symptom Score, and rectal dose-volume histogram parameters.

resultsThirty-nine patients with flare-free IBD at time of treatment (median follow-up 83.9 months) and 117 matched controls (median follow-up 88.7 months) were identified. A diagnosis of IBD was associated with increased odds of developing any late grade GI toxicity (odds ratio [OR] 6.11,

conclusionsPatients with IBD who received SBRT for PCa had a higher likelihood of developing acute GI and GU toxicity, in addition to experiencing lower grade late toxicities that occurred earlier. However, patients with IBD did not have a higher likelihood for late grade ≥2 GI or GU toxicity after SBRT compared with the control cohort. Interpretation of this data are limited by the small sample size. Thus, men with IBD in remission should be properly counseled about these risks when considering SBRT.

Identifiers

PMID34585025
PMCPMC8453194

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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.