Evidence map›Paper›PMID 32567666›Full record

ArticleJournal of radiation research2020

Risk factors for severe gastrointestinal toxicity in patients receiving palliative radiotherapy for metastatic bone tumors: association with the use of molecular-targeted agents.

Yuji Murakami, Masahiro Kenjo, Kazuki Ishikawa, Toru Sakayauchi, Satoshi Itasaka, Yoshiharu Negoro, Keiichi Jingu, Yasumasa Nishimura, Yasushi Nagata, Kazuhiko Ogawa

Open access · goldAbstract read
In one paragraph

Article in Journal of radiation research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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 7 institutions in 1 country.

Yuji MurakamiDepartment of Radiation Oncology, Hiroshima University Hospital, Hiroshima, Japan.
Masahiro KenjoHiroshima High-Precision Radiotherapy Cancer Center, Hiroshima, Japan.
Kazuki IshikawaDepartment of Radiation Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Toru SakayauchiDepartment of Radiation Oncology, Osaki Citizen Hospital, Osaki, Japan.
Satoshi ItasakaDepartment of Radiation Oncology, Kurashiki Central Hospital, Kurashiki, Japan.
Yoshiharu NegoroDepartment of Radiation Oncology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Keiichi JinguDepartment of Radiation Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yasumasa NishimuraDepartment of Radiation Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Yasushi NagataDepartment of Radiation Oncology, Hiroshima University Hospital, Hiroshima, Japan.
Kazuhiko OgawaDepartment of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Hiroshima University Hospital · JPKindai University · JPJapanese Red Cross Society Wakayama Medical Center · JPKurashiki Central Hospital · JPOsaka University · JPOsaki Citizen Hospital · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate whether the use of molecular-targeted agents could affect gastrointestinal (GI) toxicity in palliative radiotherapy (RT) for metastatic bone tumors in the abdominopelvic region. We collected data of patients who received palliative RT for bone metastases in the abdominopelvic region between 2013 and 2014 from six institutions. Data of 395 patients were collected and184 patients received molecularly targeted therapy, of whom 80 received vascular endothelial growth factor (VEGF)-targeted agents. For 556 lesions, 410 sessions of irradiation were undergone. GI toxicity of ≥G3 was observed in 3.8% of patients. The incidence rates of ≥G3 GI toxicity in patients without targeted agents use, in those using VEGF-targeted agents and in those using non-VEGF-targeted agents were 3.8, 7.5 and 1.0%, respectively. Regarding risk factors of the occurrence of ≥G3 GI toxicity, univariate analysis in all patients showed that a history of abdominopelvic surgery was a significant risk factor (P = 0.01), and the use of VEGF-targeted agents showed a trend of high incidence (P = 0.06). In patients using VEGF-targeted agents, both univariate and multivariate analysis showed that combined anticoagulant use (P = 0.03 and 0.01) and agent use between 1 week before and after RT (P = 0.046 and 0.03) were significant risk factors. In conclusion, the history of abdominopelvic surgery was associated with ≥G3 GI toxicity and the use of VEGF-targeted agents showed a trend for high incidence. When using VEGF-targeted agents, caution should be exercised in the combined use of anticoagulants and in the agent use between 1 week before and after RT.

Indexed as

Gastrointestinal TractAdultAgedAged, 80 and overAnticoagulantsBone NeoplasmsFemaleHumansIncidenceMaleMiddle AgedMolecular Targeted TherapyNeoplasm MetastasisPalliative CareRadiation InjuriesRadiation OncologyAnticoagulantsVascular Endothelial Growth Factor Abone metastasisgastrointestinal toxicitymolecularly targeted therapypalliative radiotherapyvascular endothelial growth factor-targeted agent

Identifiers

PMID32567666
PMCPMC7336816
OpenAlexW3036352594

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.