Drug-induced interstitial lung disease after chemoimmunotherapy for extensive-stage small cell lung cancer.

Drug-induced interstitial lung disease Immunotherapy Interstitial lung abnormalities Small cell lung cancer

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 19 05 2023
revised: 15 09 2023
accepted: 26 09 2023
medline: 12 10 2023
pubmed: 12 10 2023
entrez: 12 10 2023
Statut: epublish

Résumé

The combination of chemotherapy and immune checkpoint inhibitors (chemo-ICI) has become the new standard of treatment for extensive-stage small cell lung cancer (ES-SCLC). Recently, slight changes in interstitial shadows, defined as interstitial lung abnormalities (ILA), have been identified. In patients with ES-SCLC who received chemo-ICI, there are limited data on the incidence of drug-induced interstitial lung disease (D-ILD) in daily practice and the association between the development of D-ILD and ILA in the baseline computed tomography (CT). A multicenter, retrospective study was conducted to investigate the incidence of D-ILD, the risk factors for developing D-ILD, progression-free survival (PFS), and overall survival (OS) in patients with ES-SCLC who received chemo-ICI between August 2019 and November 2021. This study enrolled 70 patients (median age, 71 years; including 58 men) from nine institutions in Japan. There were 62 patients (89%) treated with carboplatin/etoposide/atezolizumab and 8 patients treated with carboplatin or cisplatin/etoposide/durvalumab. Twenty-nine patients (41.4%) were found to have ILA at baseline CT. Eleven patients (15.7%) developed D-ILD. The proportion of patients with ILA was significantly higher in the group who developed D-ILD than in the group who did not (9/11 (81.8%) vs. 20/59 (33.9%), respectively, P = 0.0057). In addition, the frequency of ground glass attenuation (GGA) and reticulation was higher in patients who developed D-ILD. There was no significant difference in PFS and OS between patients who developed D-ILD and those who did not (median PFS, 8.0 (95% confidence interval (CI), 5.5-9.5) months vs. 5.0 (95% CI, 4.5-5.6) months, respectively, P = 0.11 and median OS, not reached (NR) (95% CI, 8.7-NR) vs. 18.2 (95% CI, 13.2-NR) months, respectively, P = 0.20). The incidence of D-ILD in patients with ES-SCLC who received chemo-ICI in clinical practice was higher than that in clinical trials. Patients with pre-existing ILA were more likely to develop D-ILD.

Identifiants

pubmed: 37822623
doi: 10.1016/j.heliyon.2023.e20463
pii: S2405-8440(23)07671-5
pmc: PMC10562781
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e20463

Informations de copyright

© 2023 The Authors. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Matters requiring disclosure of COI with regard to our presentation are lecture fee by Chugai Pharmaceutical Co Ltd and research expenses from company by AstraZeneca.

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Auteurs

Kiyoko Fukuda (K)

Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.

Naoko Katsurada (N)

Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.

Yoshitaka Kawa (Y)

Department of Thoracic Oncology, Hyogo Cancer Center, Japan.

Miyako Satouchi (M)

Department of Thoracic Oncology, Hyogo Cancer Center, Japan.

Kazumi Kaneshiro (K)

Department of Respiratory Medicine, Kita-harima Medical Center, Japan.

Masataka Matsumoto (M)

Department of Respiratory Medicine, Kita-harima Medical Center, Japan.

Rei Takamiya (R)

Department of Respiratory Medicine, Akashi Medical Center, Japan.

Yukihisa Hatakeyama (Y)

Department of Respiratory Medicine, Akashi Medical Center, Japan.

Ryota Dokuni (R)

Department of Respiratory Medicine, Hyogo Prefectural Awaji Medical Center, Japan.

Kanoko Matsumura (K)

Department of Respiratory Medicine, Takatsuki General Hospital, Japan.

Masahiro Katsurada (M)

Department of Internal Medicine, Hyogo Prefectural Tamba Medical Center, Japan.

Kyosuke Nakata (K)

Department of Respiratory Medicine, Konan Medical Center, Japan.

Sho Yoshimura (S)

Department of Respiratory Medicine, Steel Memorial Hirohata Hospital, Japan.

Motoko Tachihara (M)

Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.

Classifications MeSH