Evidence map›Paper›PMID 36515701›Full record

ArticleStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2023

Systematic risk analysis of radiation pneumonitis in breast cancer: role of cotreatment with chemo-, endocrine, and targeted therapy.

Julian Mangesius, Danijela Minasch, Katharina Fink, Meinhard Nevinny-Stickel, Peter Lukas, Ute Ganswindt, Thomas Seppi

Open access · hybridAbstract read
In one paragraph

Article in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

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  9. Radiation therapy of breast cancer in the Nahe Breast Center: first results of an analysis in the context of health services research.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2024
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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

7 authors at 1 institution in 1 country.

Julian MangesiusDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria. julian.mangesius@i-med.ac.at.ORCID 0000-0003-0855-1870
Danijela MinaschDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria.
Katharina FinkDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria.
Meinhard Nevinny-StickelDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria.
Peter LukasDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria.
Ute GanswindtDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria.
Thomas SeppiDepartment of Radiation Oncology, Medical University of Innsbruck, 6020, Innsbruck, Anichstr. 35, Austria.
Innsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA major complication of sequential and concomitant chemoradiation in breast cancer treatment is interstitial pneumonitis induced by radiation therapy (RT), systemic therapy, or a combination of both. Dose and volume of co-irradiated lung tissue directly correlate with the risk of radiation pneumonitis. Especially in case of combined treatment, it is often unclear which of the used therapeutic agents promote pneumonitis.

methodsThis was a prospective monocentric study including 396 breast cancer patients. A systematic analysis of single and combined therapeutic measures was performed in order to identify treatment-related factors enhancing the risk of pneumonitis post RT.

resultsOverall incidence of pneumonitis of any grade was 38%; 28% were asymptomatic (grade 1) and 10% were symptomatic (> grade 1). Pneumonitis > grade 2 did not occur. Beside age, smoking status, and mean lung dose, the combined treatment with goserelin and tamoxifen significantly enhanced the risk of pneumonitis in a supra-additive pattern (odds ratio [OR] 4.38), whereas each agent alone or combined with other drugs only nonsignificantly contributed to a higher pneumonitis incidence post RT (OR 1.52 and OR 1.16, respectively). None of the other systemic treatments, including taxanes, increased radiation pneumonitis risk in sequential chemoradiation.

conclusionCommon treatment schedules in sequential chemoradiation following breast-conserving surgery only moderately increase lung toxicity, mainly as an asymptomatic complication, or to a minor extent, as transient pneumonitis ≤ grade 2. However, combined treatment with tamoxifen and the LHRH analog goserelin significantly increased the risk of pneumonitis in breast cancer patients after chemoradiation. Thus, closer surveillance of involved patients is advisable.

Indexed as

Breast NeoplasmsRadiation PneumonitisFemaleGoserelinHumansProspective StudiesRisk AssessmentTamoxifenGoserelinTamoxifenBreast cancerGoserelinLung toxicityNormal tissue complicationsOrgans at riskRadiation pneumonitisRadiation therapyTamoxifen

Identifiers

PMID36515701
PMCPMC9839789
OpenAlexW4311366979

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.