Evidence map›Paper›PMID 34617405›Full record

ArticleThoracic cancer2021

Dramatic, significant metabolic response to a one-time pembrolizumab treatment following a relapse of pre-existing organizing pneumonia in a patient with advanced non-small cell lung cancer: A case report.

Motoyasu Kato, Mikiko Mori, Keita Miura, Tetsuhiko Asao, Hiroaki Motomura, Koichi Nishino, Ryo Ko, Ryo Koyama, Takuo Hayashi, Kazuhisa Takahashi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Thoracic cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

10 authors at 1 institution in 1 country.

Motoyasu KatoDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-3217-5118
Mikiko MoriDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Keita MiuraDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Tetsuhiko AsaoDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Hiroaki MotomuraDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Koichi NishinoDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Ryo KoDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-2551-3529
Ryo KoyamaDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Takuo HayashiDepartment of Human Pathology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors can often trigger immune-related adverse events (irAEs), such as relapse of pre-existing interstitial pneumonia. Here, we report the case of an 88-year-Japanese man diagnosed with advanced lung adenocarcinoma with a high tumor proportion score of programmed death-ligand 1. Six years earlier, he had developed organizing pneumonia (OP), a subtype of interstitial pneumonia, that was treated with steroid pulse therapy maintained with prolonged prednisolone administration. We initiated pembrolizumab as the first-line treatment. One month after the first pembrolizumab administration, high resolution computed tomography (HRCT) of the chest demonstrated ground-glass opacities and consolidations. We suspected pembrolizumab-induced OP relapse, an irAE. His oxygenation was normal; therefore, we discontinued pembrolizumab without additional treatment for OP relapse. Four months after OP relapse, HRCT showed no new findings. After significant amelioration of OP, although the size of the tumor shadow remained the same on HRCT, positron emission tomography-computed tomography demonstrated the disappearance of the standardized uptake value of the primary tumor, mediastinal lymph nodes, and pleural nodules. In conclusion, this is the first report of a dramatic, significant metabolic response after a single pembrolizumab treatment despite the relapse of pre-existing OP in a patient with advanced lung adenocarcinoma.

Indexed as

Adenocarcinoma of LungAdrenal Cortex HormonesAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungHumansLung Diseases, InterstitialLung NeoplasmsMaleAdrenal Cortex HormonesAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunologicalpembrolizumabdrug-induced interstitial pneumoniaimmune checkpoint inhibitorsimmune-related adverse eventnon-small cell lung carcinomapembrolizumab

Identifiers

PMID34617405
PMCPMC8590898
OpenAlexW3202042047

What OpenQuestion holds

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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.