Evidence map›Paper›PMID 38613731›Full record

ArticleTargeted oncology2024

Real-World Data on Subsequent Therapy for First-Line Osimertinib-Induced Pneumonitis: Safety of EGFR-TKI Rechallenge (Osi-risk Study TORG-TG2101).

Naoya Nishioka, Hisao Imai, Masahiro Endo, Akifumi Notsu, Kosei Doshita, Satoshi Igawa, Hiroshi Yokouchi, Takashi Ninomiya, Takaaki Tokito, Sayo Soda and 28 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Targeted oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Efficacy and safety of third-generationTranslational lung cancer research · 2026
    Article
  4. Article
  5. Drug-Induced Interstitial Lung Disease in Lung Cancer Patients.Respiration; international review of thoracic diseases · 2026
    Review
  6. Article
  7. Article
  8. Observational
  9. Observational
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

38 authors at 20 institutions in 1 country.

Naoya NishiokaDivision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Hisao ImaiDepartment of Respiratory Medicine, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, Yamane 1397-1, Hidaka City, Saitama, Japan. m06701014@gunma-u.ac.jp.ORCID 0000-0003-3097-4255
Masahiro EndoDivision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Akifumi NotsuDivision of Clinical Research Center, Shizuoka Cancer Center, Shizuoka, Japan.
Kosei DoshitaDivision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Satoshi IgawaDepartment of Respiratory Medicine, Kitasato University School of Medicine, Kanagawa, Japan.
Hiroshi YokouchiDepartment of Respiratory Medicine, NHO Hokkaido Cancer Center, Hokkaido, Japan.
Takashi NinomiyaDepartment of Thoracic Oncology and Medicine, NHO Shikoku Cancer Center, Matsuyama, Ehime, Japan.
Takaaki TokitoDivision of Respirology, Neurology, and Rheumatology, Department of Internal Medicine, Kurume University School of Medicine, Fukuoka, Japan.
Sayo SodaDepartment of Pulmonary and Clinical Immunology, Dokkyo Medical University School of Medicine, Tohigi, Japan.
Takasato FujiwaraDepartment of Respiratory Internal Medicine, Yokosuka Kyosai Hospital, Kanagawa, Japan.
Tetsuhiko AsaoDepartment of Respiratory Medicine, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Shinji NakamichiDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Takahisa KawamuraDepartment of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Minehiko Inomata1st Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Kazuhisa NakashimaDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.
Kentaro ItoRespiratory Center, Matsusaka Municipal Hospital, Mie, Japan.
Yasuhiro GotoDepartment of Respiratory Medicine, Fujita Health University School of Medicine, Aichi, Japan.
Yukihiro UmedaThird Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Soichi HiraiDepartment of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Ryota UshioDepartment of Thoracic Oncology, Kanagawa Cancer Center, Kanagawa, Japan.
Keiki YokooDepartment of Respiratory Medicine, Teine Keijinkai Hospital, Hokkaido, Japan.
Takayuki TakedaDepartment of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan.
Tomoya FukuiDepartment of Respiratory Medicine, Shonan Kamakura General Hospital, Kanagawa, Japan.
Masashi IshiharaDivision of Medical Oncology, Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
Takashi OsakiDepartment of Respiratory Medicine, Shibukawa Medical Center, Gunma, Japan.
Sousuke KuboDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
Takumi FujiwaraDepartment of Genomic Medicine, Mie University Hospital, Mie, Japan.
Chie YamamotoDepartment of Respiratory Medicine, Fukuchiyama City Hospital, Kyoto, Japan.
Takeshi TsudaDivision of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Nobumasa TamuraDivision of Respiratory Diseases, Department of Internal Medicine, Atsugi City Hospital, Kanagawa, Japan.
Shinobu HosokawaDepartment of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama, Japan.
Yusuke ChiharaDepartment of Respiratory Medicine, Uji-Tokushukai Medical Center, Kyoto, Japan.
Satoshi IkedaDepartment of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Kanagawa, Japan.
Naoki FuruyaDivision of Respiratory Medicine, Department of Internal Medicine, St Marianna University School of Medicine, Kanagawa, Japan.
Yoshiro NakaharaDepartment of Respiratory Medicine, Kitasato University School of Medicine, Kanagawa, Japan.
Satoru MiuraDepartment of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.
Hiroaki OkamotoDepartment of Respiratory Medicine, Yokohama Municipal Citizen's Hospital, Yokohama, Kanagawa, Japan.
Shizuoka Cancer Center · JPKitasato University · JPKyoto Prefectural University of Medicine · JPMie University Hospital · JPDokkyo Medical University · JPFujita Health University · JPFukuyama City Hospital · JPJapanese Red Cross Society Kyoto Daini Hospital · JPJuntendo University · JPKanagawa Cardiovascular and Respiratory Center · JPKanagawa Prefectural Hospital Organization · JPKurume University · JPNiigata Cancer Center Hospital · JPNippon Medical School · JPOkayama Red Cross General Hospital · JPOsaka International Cancer Institute · JPSaitama Medical University · JPShikoku Cancer Center · JPShimane University · JPShizuoka Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough osimertinib is a promising therapeutic agent for advanced epidermal growth factor receptor (EGFR) mutation-positive lung cancer, the incidence of pneumonitis is particularly high among Japanese patients receiving the drug. Furthermore, the safety and efficacy of subsequent anticancer treatments, including EGFR-tyrosine kinase inhibitor (TKI) rechallenge, which are to be administered after pneumonitis recovery, remain unclear.

objectiveThis study investigated the safety of EGFR-TKI rechallenge in patients who experienced first-line osimertinib-induced pneumonitis, with a primary focus on recurrent pneumonitis. PATIENTS AND

methodsWe retrospectively reviewed the data of patients with EGFR mutation-positive lung cancer who developed initial pneumonitis following first-line osimertinib treatment across 34 institutions in Japan between August 2018 and September 2020.

resultsAmong the 124 patients included, 68 (54.8%) patients underwent EGFR-TKI rechallenge. The recurrence rate of pneumonitis following EGFR-TKI rechallenge was 27% (95% confidence interval [CI] 17-39) at 12 months. The cumulative incidence of recurrent pneumonitis was significantly higher in the osimertinib group than in the first- and second-generation EGFR-TKI (conventional EGFR-TKI) groups (hazard ratio [HR] 3.1; 95% CI 1.3-7.5; p = 0.013). Multivariate analysis revealed a significant association between EGFR-TKI type (osimertinib or conventional EGFR-TKI) and pneumonitis recurrence, regardless of severity or status of initial pneumonitis (HR 3.29; 95% CI 1.12-9.68; p = 0.03).

conclusionsOsimertinib rechallenge after initial pneumonitis was associated with significantly higher recurrence rates than conventional EGFR-TKI rechallenge.

Indexed as

AcrylamidesAniline CompoundsErbB ReceptorsLung NeoplasmsPneumoniaProtein Kinase InhibitorsAgedAged, 80 and overFemaleHumansIndolesJapanMaleMiddle AgedPyrimidinesRetrospective StudiesAcrylamidesAniline CompoundsEGFR protein, humanErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidines

Identifiers

PMID38613731
PMCPMC11111546
OpenAlexW4394786346

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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.