Evidence map›Paper›PMID 42645384›Full record

ArticleCurrent oncology (Toronto, Ont.)2026

Routine Inflammatory and Hematological Markers and Acute Radiation Toxicity in Patients with Prostate Cancer.

Jolanta Łuniewska-Bury, Piotr Leśniak, Adam Majchrzak, Kamil Obel, Tomasz W Kaminski, Tomasz Ząbkowski, Tomasz Syryło

Abstract read
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Article in Current oncology (Toronto, Ont.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

7 authors.

Jolanta Łuniewska-BuryFaculty of Medicine, Collegium Medicum, The Mazovian University in Płock, 2 Pl. Dąbrowskiego Street, 09-402 Płock, Poland.
Piotr LeśniakProvincial Integrated Hospital in Płock, 19 Medyczna Street, 09-400 Płock, Poland.
Adam MajchrzakDepartment of General, Functional and Oncological Urology, Military Institute of Medicine-National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Kamil ObelWarsaw Bar Association, 15/16 Żytnia Street, 01-014 Warsaw, Poland.ORCID 0000-0001-5583-3606
Tomasz W KaminskiHemostasis and Thrombosis Program, Versiti Blood Research Institute, Milwaukee, WI 53226, USA.ORCID 0000-0002-8688-4171
Tomasz ZąbkowskiDepartment of General, Functional and Oncological Urology, Military Institute of Medicine-National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.
Tomasz SyryłoDepartment of General, Functional and Oncological Urology, Military Institute of Medicine-National Research Institute, 128 Szaserów Street, 04-141 Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundModern radiotherapy techniques have improved the safety of prostate cancer treatment, but acute gastrointestinal and genitourinary toxicity remains a common clinical problem. Early identification of patients who are likely to develop treatment-related adverse effects may help optimize supportive care. This study evaluated the relationships between clinical characteristics, radiotherapy planning parameters, systemic inflammatory biomarkers, and acute pelvic toxicity during hypofractionated radiotherapy. MATERIALS AND

methodsWe retrospectively analyzed 142 patients with histologically confirmed prostate cancer who underwent external beam radiotherapy at the Provincial Integrated Hospital in Płock, Poland, between October 2024 and March 2026. Clinical, laboratory, and radiotherapy planning data were obtained from institutional electronic records. Laboratory analyses included CRP, creatinine, total leukocyte, neutrophil, lymphocyte, erythrocyte and platelet counts, hemoglobin, and hematocrit. Rectal and bladder toxicity was prospectively graded according to the RTOG/EORTC criteria at 2 and 4 weeks after treatment initiation. Correlation and multivariable regression analyses were performed to identify factors associated with acute treatment-related toxicity.

resultsRadiotherapy significantly reduced leukocyte and lymphocyte counts (both

conclusionsEarly gastrointestinal and genitourinary toxicity appears to be a useful clinical indicator of persistent treatment-related symptoms during hypofractionated prostate radiotherapy. Early rectal and bladder toxicity was associated with toxicity later during treatment, whereas routine laboratory markers and most dosimetric parameters showed limited independent associations with acute pelvic toxicity.

Indexed as

InflammationProstatic NeoplasmsRadiation InjuriesAgedAged, 80 and overBiomarkersHumansMaleMiddle AgedRetrospective StudiesBiomarkersacute pelvic toxicityhypofractionated radiotherapyinflammatory biomarkersprostate cancer

Identifiers

PMID42645384
PMCPMC13510397

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