Evidence map›Paper›PMID 36551668›Full record

ArticleCancers2022

The Effect of Pleural Effusion on Prognosis in Patients with Non-Small Cell Lung Cancer Undergoing Immunochemotherapy: A Retrospective Observational Study.

Tomoka Nishimura, Eiki Ichihara, Toshihide Yokoyama, Koji Inoue, Tomoki Tamura, Ken Sato, Naohiro Oda, Hirohisa Kano, Daizo Kishino, Haruyuki Kawai and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

18 authors at 14 institutions in 1 country.

Tomoka NishimuraDepartment of Hematology and Oncology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama 700-8558, Japan.
Eiki IchiharaDepartment of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama 700-8558, Japan.ORCID 0000-0002-2966-106X
Toshihide YokoyamaDepartment of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, Kurashiki 710-8602, Japan.
Koji InoueDepartment of Respiratory Medicine, Ehime Prefectural Central Hospital, Matsuyma 790-0024, Japan.
Tomoki TamuraDepartment of Respiratory Medicine, NHO Iwakuni Clinical Center, Iwakuni 740-8510, Japan.ORCID 0000-0002-2480-9029
Ken SatoDepartment of Respiratory Medicine, National Hospital Organization Okayama Medical Center, Okayama 701-1192, Japan.
Naohiro OdaDepartment of Internal Medicine, Fukuyama City Hospital, Fukuyama 721-8511, Japan.
Hirohisa KanoDepartment of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama 700-8607, Japan.ORCID 0000-0003-4327-7547
Daizo KishinoDepartment of Respiratory Medicine, Japanese Red Cross Society Himeji Hospital, Himeji 670-8540, Japan.
Haruyuki KawaiDepartment of Internal Medicine, Okayama Saiseikai General Hospital, Okayama 700-0021, Japan.ORCID 0000-0001-7129-5377
Masaaki InoueDepartment of Chest Surgery, Shimonoseki City Hospital, Shimonoseki 750-8520, Japan.
Nobuaki OchiDepartment of General Internal Medicine 4, Kawasaki Medical School, Okayama 700-8505, Japan.
Nobukazu FujimotoDepartment of Respiratory Medicine, Okayama Rosai Hospital, Okayama 702-8055, Japan.
Hirohisa IchikawaDepartment of Respiratory Medicine, KKR Takamatsu Hospital, Takamatsu 760-0018, Japan.
Chihiro AndoDepartment of Hematology and Oncology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama 700-8558, Japan.ORCID 0000-0003-3775-7536
Katsuyuki HottaCenter for Innovative Clinical Medicine, Okayama University Hospital, Okayama 700-8558, Japan.
Yoshinobu MaedaDepartment of Hematology and Oncology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama 700-8558, Japan.
Katsuyuki KiuraDepartment of Allergy and Respiratory Medicine, Okayama University Hospital, Okayama 700-8558, Japan.
Okayama University · JPOkayama University Hospital · JPEhime Prefectural Central Hospital · JPFukuyama City Hospital · JPHimeji Red Cross Hospital · JPIwakuni Medical Center · JPKawasaki Medical School · JPKurashiki Central Hospital · JPNational Hospital Organization · JPNational Hospital Organization Takamatsu Medical Center · JPOkayama Red Cross General Hospital · JPOkayama Rosai Hospital · JPOkayama Saiseikai General Hospital · JPShimonoseki City Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Combined immune checkpoint inhibitor (ICI) therapy and chemotherapy has become the standard treatment for advanced non-small-cell lung cancer (NSCLC). Pleural effusion (PE) is associated with poor outcomes among patients with NSCLC undergoing chemotherapy. However, minimal data exists on PE for patients undergoing combined ICI and chemotherapy. Therefore, we investigated how PE affects survival outcomes in patients with NSCLC undergoing this combined therapy. Methods: We identified patients with advanced NSCLC undergoing chemotherapy and ICI therapy from the Okayama Lung Cancer Study Group−Immune Chemotherapy Database (OLCSG−ICD) between December 2018 and December 2020; the OLCSG−ICD includes the clinical data of patients with advanced NSCLC from 13 institutions. Then, we analyzed the treatment outcomes based on the presence of PE. Results: We identified 478 patients who underwent combined ICI therapy and chemotherapy; 357 patients did not have PE, and 121 patients did have PE. Patients with PE had significantly shorter progression-free survival (PFS) and overall survival (OS) than those without PE (median PFS: 6.2 months versus 9.1 months; p < 0.001; median OS: 16.4 months versus 27.7 months; p < 0.001). The negative effect of PE differed based on the patient’s programmed cell death-ligand 1 (PD-L1) expression status; with the effect being more evident in patients with high PD-L1 expression. In addition, PFS and OS did not differ between patients who did and did not undergo bevacizumab treatment; thus, bevacizumab-containing regimens did not improve the survival outcomes for patients with PE. Conclusion: PE is associated with poor outcomes among patients with NSCLC undergoing combined ICI therapy and chemotherapy.

Indexed as

immune checkpoint inhibitorsnon-small cell carcinomapleural effusion

Identifiers

PMID36551668
PMCPMC9776517
OpenAlexW4311794139

What OpenQuestion holds

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LicenceCC BY
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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.