Evidence map›Paper›PMID 38651033›Full record

ArticleJTO clinical and research reports2024

The Tumor Immune Microenvironment Is Associated With Recurrence in Early-Stage Lung Adenocarcinoma.

Hiroaki Kanemura, Toshihide Yokoyama, Ryu Nakajima, Atsushi Nakamura, Hiroaki Kuroda, Yoshitaka Kitamura, Hiroyasu Shoda, Nobuaki Mamesaya, Yoshihiro Miyata, Tatsuro Okamoto and 20 more

Open access · goldAbstract read
In one paragraph

Article in JTO clinical and research reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. CD4Translational lung cancer research · 2026
    Article
  3. Article
  4. Article
  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

30 authors at 20 institutions in 1 country.

Hiroaki KanemuraDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Toshihide YokoyamaDepartment of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.
Ryu NakajimaDepartment of General Thoracic Surgery, Osaka City General Hospital, Osaka, Japan.
Atsushi NakamuraDepartment of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan.
Hiroaki KurodaDepartment of Thoracic Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
Yoshitaka KitamuraDivision of Chest Surgery, Hyogo Cancer Center, Akashi, Japan.
Hiroyasu ShodaDepartment of Respiratory Medicine, Hiroshima City Hiroshima Citizen Hospital, Hiroshima, Japan.
Nobuaki MamesayaDivision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Yoshihiro MiyataDepartment of Surgical Oncology, Hiroshima University, Hiroshima, Japan.
Tatsuro OkamotoDepartment of Thoracic Oncology, NHO Kyushu Cancer Center, Fukuoka, Japan.
Kyoichi OkishioDepartment of Clinical Research Center, NHO Kinki Chuo Chest Medical Center, Osaka, Japan.
Masahide OkiDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Yuichi SakairiDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Toyofumi Fengshi Chen-YoshikawaDepartment of Thoracic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Tadashi AokiDepartment of Chest Surgery, Niigata Cancer Center Hospital, Niigata, Japan.
Tatsuo OhiraDepartment of Surgery, Tokyo Medical University, Tokyo, Japan.
Isao MatsumotoDepartment of Thoracic Surgery, Kanazawa University, Kanazawa, Japan.
Kiyonobu UenoDepartment of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.
Takuro MiyazakiDepartment of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Haruhisa MatsugumaDepartment of Thoracic Surgery, Tochigi Cancer Center, Utsunomiya, Japan.
Hideoki YokouchiDepartment of Surgery, Suita Municipal Hospital, Osaka, Japan.
Tomoyuki OtaniDepartment of Pathology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Akihiko ItoDepartment of Pathology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kazuko SakaiDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Yasutaka ChibaClinical Research Center, Kindai University Hospital, Osaka-Sayama, Japan.
Kazuto NishioDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Nobuyuki YamamotoInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Isamu OkamotoDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Kazuhiko NakagawaDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Masayuki TakedaDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kindai University · JPOsaka City General Hospital · JPAichi Cancer Center · JPChiba University · JPHiroshima City Asa Citizens Hospital · JPHiroshima University · JPHyogo Prefectural Cancer Center · JPKanazawa University · JPKindai University Hospital · JPKurashiki Central Hospital · JPKyushu University · JPNagasaki University · JPNagoya Medical Center · JPNagoya University · JPNara Medical University · JPNational Hospital Organization Kyushu Cancer Center · JPNational Kinki Chuo Hospital for Chest Disease · JPNiigata Cancer Center Hospital · JPSendai Kousei Hospital · JPShizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Immune checkpoint inhibitors have recently been approved for the treatment of early-stage NSCLC in the perioperative setting on the basis of phase 3 trials. However, the characteristics of such patients who are susceptible to recurrence after adjuvant chemotherapy or who are likely to benefit from postoperative immunotherapy have remained unclear. Methods: This biomarker study (WJOG12219LTR) was designed to evaluate cancer stem cell markers (CD44 and CD133), programmed death-ligand 1 (PD-L1) expression on tumor cells, CD8 expression on tumor-infiltrating lymphocytes, and tumor mutation burden in completely resected stage II to IIIA NSCLC with the use of archived DNA and tissue samples from the prospective WJOG4107 trial. Tumors were classified as inflamed or noninflamed on the basis of the PD-L1 tumor proportion score and CD8 Results: A total of 117 patients were included in this study. The median RFS was not reached (95% confidence intervals [CI]: 22.4 mo-not reached; n = 39) and 23.7 months (95% CI: 14.5-43.6; n = 41) in patients with inflamed or noninflamed adenocarcinoma, respectively (log-rank Conclusions: PD-L1 expression on tumor cells, CD8

Indexed as

Adjuvant chemotherapyCancer stem cellNon–small cell lung cancerTumor immune microenvironment

Identifiers

PMID38651033
PMCPMC11033192
OpenAlexW4392593851

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.