Evidence map›Paper›PMID 40688713›Full record

ArticleRespiratory medicine case reports2025

Severe drug-induced interstitial lung disease after photoimmunotherapy with cetuximab-sarotalocan sodium in a patient with oropharyngeal cancer: A case report.

Sho Takuma, Masato Karayama, Risa Suzuki, Koichi Miyashita, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Yuzo Suzuki, Kazuki Furuhashi, Noriyuki Enomoto and 3 more

Abstract readCase Reports
In one paragraph

Article in Respiratory medicine case reports, 2025. 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

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

2 citing papers in PubMed.

  1. Review
  2. Review
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

13 authors.

Sho TakumaSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Masato KarayamaSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Risa SuzukiSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Koichi MiyashitaSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Yusuke InoueSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Hideki YasuiSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Hironao HozumiSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Yuzo SuzukiSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Kazuki FuruhashiSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Noriyuki EnomotoSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Tomoyuki FujisawaSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Naoki InuiSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.
Takafumi SudaSecond Division, Department of Internal Medicine, School of Medicine, Hamamatsu University, 1-20-1 Handayama Chuoku, Hamamatsu, 431-3192, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Photoimmunotherapy (PIT) using cetuximab-sarotalocan sodium (CS) is a novel therapy for unresectable or locally recurrent head and neck squamous cell carcinoma (HNSCC). CS is a conjugate of cetuximab (monoclonal antibody targeting epidermal growth factor receptor [EGFR]) and IR700 (light-activatable dye). Intravenously administered CS binds to cancer cells expressing EGFR. Upon exposure to a 690 nm wavelength laser, the conjugated IR700 is photoactivated and induces a photochemical reaction that damages the tumor cells. While CS-PIT showed a favorable safety profile in an HNSCC clinical trial with no cases of drug-induced interstitial lung disease (DIILD), cetuximab is known to cause DIILD, especially in patients with pre-existing interstitial lung disease (ILD). Case presentation: A 79-year-old man with recurrent HNSCC after surgery and adjuvant chemoradiotherapy received CS-PIT. Pre-treatment high-resolution chest computed tomography (HRCT) revealed mild ILD in the lower lobes of both lungs. Two months after CS-PIT, he developed severe DIILD with hypoxia. He received two cycles of intravenous methylprednisolone (1 g/day, 3 days/cycle) followed by oral prednisolone at 1 mg/kg/day, which was gradually tapered. After the high-dose corticosteroid therapy, the DIILD improved. Conclusion: We report the first case of DIILD caused by CS-PIT. Because cetuximab is a component of CS, CS-PIT has the potential to induce DIILD. Risk assessments and monitoring for DIILD are recommended for patients receiving CS-PIT.

Indexed as

CetuximabCetuximab-sarotalocan sodiumDrug-induced interstitial lung diseaseInterstitial pneumoniaLung injuryPhotoimmunotherapyPneumonitis

Identifiers

PMID40688713
PMCPMC12275018

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.