Evidence map›Paper›PMID 36551721›Full record

ArticleCancers2022

Pre-Existing Interstitial Lung Abnormalities Are Independent Risk Factors for Interstitial Lung Disease during Durvalumab Treatment after Chemoradiotherapy in Patients with Locally Advanced Non-Small-Cell Lung Cancer.

Wakako Daido, Takeshi Masuda, Nobuki Imano, Naoko Matsumoto, Kosuke Hamai, Yasuo Iwamoto, Yusuke Takayama, Sayaka Ueno, Masahiko Sumii, Hiroyasu Shoda and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 13% 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, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

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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

21 authors at 9 institutions in 1 country.

Wakako DaidoDepartment of Respiratory Medicine, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Takeshi MasudaDepartment of Respiratory Medicine, Hiroshima University Hospital, Hiroshima 734-8551, Japan.ORCID 0000-0003-3557-0049
Nobuki ImanoDepartment of Radiation Oncology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Naoko MatsumotoDepartment of Respiratory Internal Medicine, Hiroshima Red Cross Hospital & Atomic-Bomb Survivors Hospital, Hiroshima 730-8619, Japan.
Kosuke HamaiDepartment of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima 734-8530, Japan.
Yasuo IwamotoDepartment of Medical Oncology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima 730-8518, Japan.
Yusuke TakayamaDepartment of Respiratory Internal Medicine, Hiroshima City Hiroshima Citizens Hospital, Hiroshima 730-8518, Japan.
Sayaka UenoDepartment of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima 734-8530, Japan.
Masahiko SumiiDepartment of Respiratory Medicine, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Hiroyasu ShodaDepartment of Respiratory Internal Medicine, Hiroshima City Hiroshima Citizens Hospital, Hiroshima 730-8518, Japan.
Nobuhisa IshikawaDepartment of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima 734-8530, Japan.
Masahiro YamasakiDepartment of Respiratory Internal Medicine, Hiroshima Red Cross Hospital & Atomic-Bomb Survivors Hospital, Hiroshima 730-8619, Japan.
Yoshifumi NishimuraDepartment of Respiratory Medicine, National Hospital Organization Higashihiroshima Medical Center, Hiroshima 739-0041, Japan.
Shigeo KawaseDepartment of Respiratory Medicine, Kure Kyosai Hospital, Hiroshima 737-8505, Japan.
Naoki ShiotaDepartment of Respiratory Disease, Chugoku Rousai General Hospital, Hiroshima 737-0193, Japan.
Yoshikazu AwayaDepartment of Respiratory Medicine, Miyoshi Central Hospital, Hiroshima 728-8502, Japan.
Tomoko SuzukiDepartment of Respiratory Medicine, JA Onomichi General Hospital, Hiroshima 722-8508, Japan.
Soichi KitaguchiDepartment of Respiratory Internal Medicine, Hiroshima City North Medical Center Asa Citizens Hospital, Hiroshima 731-0232, Japan.
Kazunori FujitakaDepartment of Respiratory Medicine, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Yasushi NagataDepartment of Radiation Oncology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Noboru HattoriDepartment of Respiratory Medicine, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Hiroshima University Hospital · JPHiroshima City Asa Citizens Hospital · JPHiroshima Prefectural Hospital · JPHiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital · JPChugoku Rosai Hospital · JPHigashihiroshima Medical Center · JPKure Kyosai Hospital · JPMiyoshi Kasei (Japan) · JPOnomichi General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction/Background: Chemoradiotherapy (CRT) followed by durvalumab, an immune checkpoint inhibitor, is the standard treatment for locally advanced non-small-cell lung cancer (NSCLC). Interstitial lung disease (ILD) is a life-threatening toxicity caused by these treatments; however, risk factors for the ILD have not yet been established. Interstitial lung abnormalities (ILAs) are computed tomography (CT) findings which manifest as minor interstitial shadows. We aimed to investigate whether ILAs could be risk factors for grade-two or higher ILD during durvalumab therapy. Patients and Methods: Patients with NSCLC who received durvalumab after CRT from July 2018 to June 2021 were retrospectively enrolled. We obtained patient characteristics, laboratory data, radiotherapeutic parameters, and chest CT findings before durvalumab therapy. Results: A total of 148 patients were enrolled. The prevalence of ILAs before durvalumab treatment was 37.8%. Among 148 patients, 63.5% developed ILD during durvalumab therapy. The proportion of patients with grade-two or higher ILD was 33.8%. The univariate logistic regression analysis revealed that older age, high dose-volume histogram parameters, and the presence of ILAs were significant risk factors for grade-two or higher ILD. The multivariate analysis showed that ILAs were independent risk factors for grade-two or higher ILD (odds ratio, 3.70; 95% confidence interval, 1.69−7.72; p < 0.001). Conclusions: We showed that pre-existing ILAs are risk factors for ILD during durvalumab treatment after CRT. We should pay attention to the development of grade-two or higher ILD during durvalumab treatment in patients with ILAs.

Indexed as

chemoradiotherapydurvalumabinterstitial lung abnormalitiesinterstitial lung disease

Identifiers

PMID36551721
PMCPMC9776853
OpenAlexW4312140716

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.