Evidence map›Paper›PMID 31784866›Full record

ArticleInvestigational new drugs2020

Association between metastatic sites and first-line pembrolizumab treatment outcome for advanced non-small cell lung cancer with high PD-L1 expression: a retrospective multicenter cohort study.

Hayato Kawachi, Motohiro Tamiya, Akihiro Tamiya, Seigo Ishii, Katsuya Hirano, Hirotaka Matsumoto, Yasushi Fukuda, Toshihide Yokoyama, Ryota Kominami, Daichi Fujimoto and 10 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Investigational new drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 3 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Impact of bone metastasis on the prognosis of non-small cell lung cancer patients treated with immune checkpoint inhibitors: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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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

20 authors at 11 institutions in 1 country.

Hayato KawachiDepartment of Thoracic Oncology, Osaka International Cancer Institute, 3-1-69 Otemachi, Osaka, 541-8567, Japan.
Motohiro TamiyaDepartment of Thoracic Oncology, Osaka International Cancer Institute, 3-1-69 Otemachi, Osaka, 541-8567, Japan. moto19781205@yahoo.co.jp.ORCID http://orcid.org/0000-0001-6529-3092
Akihiro TamiyaDepartment of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Seigo IshiiDepartment of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Katsuya HiranoDepartment of Respiratory Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
Hirotaka MatsumotoDepartment of Respiratory Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
Yasushi FukudaDepartment of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.
Toshihide YokoyamaDepartment of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.
Ryota KominamiDepartment of Respiratory Medicine, National Hospital Organization Himeji Medical Center, Himeji, Japan.
Daichi FujimotoDepartment of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
Kazutaka HosoyaDepartment of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
Hidekazu SuzukiDepartment of Thoracic Oncology, Osaka Habikino Medical Center, Habikino, Japan.
Tomonori HirashimaDepartment of Thoracic Oncology, Osaka Habikino Medical Center, Habikino, Japan.
Masaki KanazuDepartment of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Toyonaka, Japan.
Nobuhiko SawaDepartment of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Toyonaka, Japan.
Junji UchidaDepartment of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.
Mitsunori MoritaDepartment of Respiratory Medicine, Kobe City Medical Center West Hospital, Kobe, Japan.
Takeshi MakioDepartment of Respiratory Medicine, Itami City Hospital, Itami, Japan.
Satoshi HaraDepartment of Respiratory Medicine, Itami City Hospital, Itami, Japan.
Toru KumagaiDepartment of Thoracic Oncology, Osaka International Cancer Institute, 3-1-69 Otemachi, Osaka, 541-8567, Japan.
Osaka Prefectural Medical Center · JPHyogo Prefectural Amagasaki General Medical Center · JPItami City Hospital · JPKobe City Medical Center General Hospital · JPKurashiki Central Hospital · JPNHO Kinki Chuo Chest Medical Center · JPOsaka International Cancer Institute · JPToneyama National Hospital · JPHimeji Medical Center · JPKobe City Medical Center West Hospital · JPOsaka International Cancer Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Associations between treatment outcomes of immune checkpoint inhibitors and metastatic sites in advanced non-small cell lung cancer (NSCLC) are not well known. Therefore, this multicenter retrospective study aimed to investigate the predictive factors of metastatic sites after first-line pembrolizumab treatment for advanced NSCLC with a PD-L1 tumor proportion score (TPS) ≥50%. We retrospectively analyzed advanced NSCLC patients with a PD-L1 TPS ≥50% who underwent first-line pembrolizumab therapy at 11 institutions between February 2017 and April 2018. Clinical data collected from medical records included metastatic sites at the time of pembrolizumab treatment. Treatment outcomes of pembrolizumab were assessed according to the Response Evaluation Criteria in Solid Tumors, version 1.1. In total, 213 patients were included in the study. The median age was 71 years (range 39-91 years). Of the 213 patients, 176 (83%) were men and 172 (81%) had an Eastern Cooperative Oncology Group performance status (ECOG-PS) score of 0-1. The most common metastases were thoracic lymph node metastasis (77%), intrapulmonary metastasis (31%), bone metastasis (28%), and malignant pleural effusion (26%). On multivariate analysis, a poor ECOG-PS score (hazard ratio: 1.95, 95.0% confidence interval: 1.25-3.04; P = 0.003) and malignant pleural effusion (hazard ratio: 1.52, 95.0% confidence interval: 1.01-2.29; P = 0.043) were independent predictors of shorter progression-free survival in patients treated with pembrolizumab. For NSCLC patients with malignant pleural effusion, pembrolizumab monotherapy is not a suitable first-line treatment because of its insufficient effectiveness, even though their PD-L1 TPS was high.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellFemaleFollow-Up StudiesHumansLung NeoplasmsMaleMiddle AgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorCD274 protein, humanpembrolizumabImmune checkpoint inhibitorMetastatic siteNon-small cell lung cancerPembrolizumabTreatment outcome

Identifiers

PMID31784866
OpenAlexW2991387714

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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.