Evidence map›Paper›PMID 36340451›Full record

ArticleCancer diagnosis & prognosis

Comparison of Late Toxicity After Whole-pelvis

Ryo Ogino, Kentaro Ishii, Toshifumi Nakajima, Yukinari Hosokawa, Kazuki Kubo, Reiko Takemura, Hideyuki Morimoto, Shogo Matsuda, Ryu Kawamorita, Takuhito Tada

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In one paragraph

Article in Cancer diagnosis & prognosis. 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
0.2field-weighted citation impact, top 47% of its field
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, 1 citations in OpenAlex.

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

10 authors at 4 institutions in 1 country.

Ryo OginoDepartment of Radiology, National Hospital Organization Osaka Minami Medical Center, Osaka, Japan.
Kentaro IshiiDepartment of Radiation Oncology, Tane General Hospital, Osaka, Japan.
Toshifumi NakajimaDepartment of Radiation Oncology, Tane General Hospital, Osaka, Japan.
Yukinari HosokawaDepartment of Urology, Tane General Hospital, Osaka, Japan.
Kazuki KuboDepartment of Medical Physics, Graduate School of Medical Sciences, Kindai University, Osaka, Japan.
Reiko TakemuraDepartment of Radiation Oncology, Tane General Hospital, Osaka, Japan.
Hideyuki MorimotoDepartment of Radiation Oncology, Tane General Hospital, Osaka, Japan.
Shogo MatsudaDepartment of Radiation Oncology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Ryu KawamoritaDepartment of Radiation Oncology, Tane General Hospital, Osaka, Japan.
Takuhito TadaDepartment of Radiology, Izumi City General Hospital, Izumi, Japan.
Tane General Hospital · JPIzumi City General Hospital · JPKindai University · JPOsaka Minami Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimTo evaluate whether whole-pelvis (WP) volumetric modulated arc therapy (VMAT) is associated with increased late toxicity compared with prostate-only (PO) VMAT in patients with localized prostate cancer. PATIENTS AND

methodsParticipants comprised 384 consecutive patients treated with definitive VMAT to 78 Gy in 39 fractions from July 2011 to August 2016. Of these, 183 patients received PO-VMAT and 201 patients received initial WP-VMAT to 46.8 Gy in 26 fractions using a simultaneous integrated boost technique. Gastrointestinal (GI) and genitourinary (GU) toxicities were prospectively scored using Common Terminology Criteria for Adverse Events version 4.0.

resultsMedian follow-up was 49 months (range=16-88 months) in the PO-VMAT group and 52 months (range=10-85 months) in the WP-VMAT group. Frequencies of Grade 3 late GI and GU toxicities were ≤3% across both groups. No patients experienced Grade 4+ toxicity. Cumulative incidences of Grade 2+ late GI and GU toxicities were similar between PO- and WP-VMAT groups (p=0.508 and p=0.838, respectively). Five-year cumulative incidences of Grade 2+ late GI and GU toxicities were 12.2% and 6.6% for the PO-VMAT group and 12.3% and 8.9% for the WP-VMAT group, respectively.

conclusionWP-VMAT did not increase late GI and GU toxicities. This suggests that concerns about increasing toxicity profile are insufficient reason for omitting WPRT for patients with high-risk prostate cancer.

Indexed as

late toxicityProstate cancerVMATwhole-pelvis irradiation

Identifiers

PMID36340451
PMCPMC9628145
OpenAlexW4308555173

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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.