Evidence map›Paper›PMID 39234190›Full record

ArticleOncoTargets and therapy2024

Safety and Efficacy of Gefitinib Administration After Osimertinib-Induced Interstitial Lung Disease: A Six-Case Series.

Kaoruko Shimbu, Kakeru Hisakane, Naohiro Kadoma, Shunichi Nishima, Kenichiro Atsumi, Masahiro Seike, Takashi Hirose

Abstract readCase Reports
In one paragraph

Article in OncoTargets and therapy, 2024. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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.

  1. Article
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4 · The record

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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.

Kaoruko ShimbuDepartment of Pulmonary Medicine and Medical Oncology, Nippon Medical School, Tama Nagayama Hospital, Tokyo, 206-8512, Japan.
Kakeru HisakaneDepartment of Pulmonary Medicine and Medical Oncology, Nippon Medical School, Tama Nagayama Hospital, Tokyo, 206-8512, Japan.ORCID 0000-0002-9108-2050
Naohiro KadomaDepartment of Pulmonary Medicine and Medical Oncology, Nippon Medical School, Tama Nagayama Hospital, Tokyo, 206-8512, Japan.ORCID 0009-0006-3938-5317
Shunichi NishimaDepartment of Pulmonary Medicine and Medical Oncology, Nippon Medical School, Tama Nagayama Hospital, Tokyo, 206-8512, Japan.
Kenichiro AtsumiDepartment of Pulmonary Medicine and Medical Oncology, Nippon Medical School, Tama Nagayama Hospital, Tokyo, 206-8512, Japan.ORCID 0000-0003-1264-0227
Masahiro SeikeDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, 113-8603, Japan.
Takashi HiroseDepartment of Pulmonary Medicine and Medical Oncology, Nippon Medical School, Tama Nagayama Hospital, Tokyo, 206-8512, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Osimertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, is the standard treatment for patients with non-small cell lung cancer harboring EGFR mutations. Although the frequency of osimertinib-induced interstitial lung disease (osi-ILD) is high, the optimal cancer treatment after osi-ILD has not been established. This time, we focused on the safety and efficacy of gefitinib following osi-ILD. Case Presentation: We experienced six cases (five women and one man; median age: 74 years) in which gefitinib was administered after osi-ILD. All six cases had grade 2 or higher osi-ILD and required steroid treatment. The computed tomography imaging pattern of osi-ILD revealed organizing pneumonia in three cases, diffuse alveolar damage in two cases, and hypersensitivity pneumonia in one case. Eastern Cooperative Oncology Group performance status was 1 in four cases, 2 in one case, and 3 in one case. EGFR mutation status was exon 19 deletion in two cases and exon 21 L858R in four cases. Only one patient experienced recurrence of ILD after receiving gefitinib. The best response to gefitinib was partial response in two cases and stable disease in three cases; one case was not evaluable. The median progression-free survival after treatment with gefitinib was 190 days (95% confidence interval: 33-328). Conclusion: The treatment with gefitinib after the development of osi-ILD was safe and effective. Gefitinib may be a promising option for patients who recovered from severe osi-ILD.

Indexed as

chemotherapyepidermal growth factor receptor kinase inhibitornon-small cell lung cancersteroid

Identifiers

PMID39234190
PMCPMC11371895

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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.