Evidence map›Paper›PMID 41349223›Full record

Observational studyESMO open2025

Real-world evaluation of interstitial lung disease/pneumonitis in patients treated with trastuzumab deruxtecan for HER2-positive advanced or recurrent gastric cancer: a postmarketing surveillance study in Japan.

H Kawakami, K Uchino, W Hashimoto, K Muro

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in ESMO open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Observational
  5. 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

4 authors.

H KawakamiDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka, Japan; Department of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan. Electronic address: kawakami_h@tohoku.ac.jp.
K UchinoPharmacoepidemiology & PMS Department, Daiichi Sankyo Co. Ltd., Tokyo, Japan.
W HashimotoData Intelligence Department, Daiichi Sankyo Co. Ltd., Tokyo, Japan.
K MuroDepartment of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterstitial lung disease (ILD)/pneumonitis is an important identified risk associated with trastuzumab deruxtecan (T-DXd) treatment, but there are few reports of T-DXd-related ILD in a real-world setting. MATERIALS AND

methodsThis observational, multicenter, all-patient postmarketing surveillance study in patients with gastric cancer treated with T-DXd in a real-world setting in Japan investigated the incidence and characteristics of drug-related ILD and factors of interest associated with its incidence. All patients who initiated T-DXd treatment for human epidermal growth factor receptor 2 (HER2)-positive unresectable advanced or recurrent gastric cancer between September 2020 and December 2021 were enrolled and observed until T-DXd therapy termination or completion of 12 months of treatment. All potential ILD cases occurring during or after T-DXd treatment were reported by the investigators and evaluated. The primary outcome was adjudicated drug-related ILD.

resultsIn the safety analysis set (n = 1070), 77.4% were males and the median age was 70 years (range 23-100 years). The median treatment duration of T-DXd was 3.9 months (range 0.7-12.0 months). The incidence of any grade, grade ≥3, and grade 5 adjudicated drug-related ILD was 9.6%, 2.8%, and 1.2%, respectively. The median time from first T-DXd treatment to the first onset of adjudicated drug-related ILD episode was 2.9 months (range 0.3-11.5 months). The most common imaging pattern at the onset of adjudicated drug-related ILD was organizing pneumonia (62.1%), followed by hypersensitivity pneumonitis (20.4%) and diffuse alveolar damage (7.8%). Age (≥75 years), medical history and/or comorbidity of ILD, radiation pneumonitis, and chronic obstructive pulmonary disease (COPD) or emphysema were identified as factors of interest for ILD incidence.

conclusionThe incidence of ILD with T-DXd in the real-world setting was similar to that observed in clinical trials, indicating no new ILD-related safety signals. Further investigation of the identified factors may offer insights into ILD incidence in high-risk populations.

Indexed as

CamptothecinImmunoconjugatesLung Diseases, InterstitialPneumoniaStomach NeoplasmsTrastuzumabAdultAgedAged, 80 and overErb-b2 Receptor Tyrosine KinasesFemaleHumansIncidenceJapanMaleMiddle AgedCamptothecinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmunoconjugatesTrastuzumabtrastuzumab deruxtecangastric cancerHER2-positiveinterstitial lung diseasepostmarketing surveillancetrastuzumab deruxtecan

Identifiers

PMID41349223
PMCPMC12800766

What OpenQuestion holds

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Registered trials

None linked

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.