Evidence map›Paper›PMID 37217919›Full record

ArticleRadiation oncology (London, England)2023

Clinical features and risk factors for interstitial lung disease spreading in low-dose irradiated areas after definitive radiotherapy with or without durvalumab consolidation therapy for patients with non-small cell lung cancer.

Mai Sakagami, Haruo Inokuchi, Nobutaka Mukumoto, Hiroshige Itoyama, Nobunari Hamaura, Mutsumi Yamagishi, Naoki Mukumoto, Shogo Matsuda, Daijiro Kabata, Keiko Shibuya

Open access · goldAbstract read
In one paragraph

Article in Radiation oncology (London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 83% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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 3 institutions in 1 country.

Mai SakagamiDepartment of Radiation Oncology, Graduate School of Medicine, Osaka City University, Osaka, Japan. o21064c@omu.ac.jp.
Haruo InokuchiDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Nobutaka MukumotoDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Hiroshige ItoyamaDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Nobunari HamauraDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Mutsumi YamagishiDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Naoki MukumotoDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Shogo MatsudaDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Daijiro KabataDepartment of Medical Statistics, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Keiko ShibuyaDepartment of Radiation Oncology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Tokyo Metropolitan University · JPOsaka Metropolitan UniversityOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe current standard of care for patients with unresectable locally advanced non-small cell lung cancer (NSCLC) is chemoradiotherapy (CRT) combined with durvalumab consolidation therapy. However, radiotherapy (RT) always carries the risk of radiation pneumonitis (RP), which can preclude durvalumab continuation. In particular, the spread of interstitial lung disease (ILD) in low-dose areas or extending beyond the RT field often makes it difficult to determine the safety of continuation or rechallenging of durvalumab. Thus, we retrospectively analyzed ILD/RP after definitive RT with and without durvalumab, with assessment of radiologic features and dose distribution in RT.

methodsWe retrospectively evaluated the clinical records, CT imaging, and radiotherapy planning data of 74 patients with NSCLC who underwent definitive RT at our institution between July 2016 and July 2020. We assessed the risk factors for recurrence within one year and occurrence of ILD/RP.

resultsKaplan-Meier method showed that ≥ 7 cycles of durvalumab significantly improved 1-year progression free survival (PFS) (p < 0.001). Nineteen patients (26%) were diagnosed with ≥ Grade 2 and 7 (9.5%) with ≥ Grade 3 ILD/RP after completing RT. There was no significant correlation between durvalumab administration and ≥ Grade 2 ILD/RP. Twelve patients (16%) developed ILD/RP that spread outside the high-dose (> 40 Gy) area, of whom 8 (67%) had ≥ Grade 2 and 3 (25%) had Grade 3 symptoms. In unadjusted and multivariate Cox proportional-hazards models adjusted for V

conclusionsDurvalumab improved 1-year PFS without increasing the risk of ILD/RP. Diabetic factors were associated with ILD/RP distribution pattern spreading in the lower dose area or outside RT fields, with a high rate of symptoms. Further study of the clinical background of patients including diabetes is needed to safely increase the number of durvalumab doses after CRT.

Indexed as

Carcinoma, Non-Small-Cell LungLung Diseases, InterstitialLung NeoplasmsRadiation PneumonitisAntibodies, MonoclonalChemoradiotherapyConsolidation ChemotherapyHumansRetrospective StudiesRisk FactorsAntibodies, MonoclonaldurvalumabChemoradiotherapyDiabetesDurvalumabInterstitial lung diseaseNon-small cell lung cancerRadiation pneumonitisRadiotherapyRisk factor

Identifiers

PMID37217919
PMCPMC10204233
OpenAlexW4377291352

What Socratic 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 Socratic graph.