Evidence map›Paper›PMID 34845792›Full record

Observational studyCancer science2022

Alpha-actinin-4 (ACTN4) gene amplification is a predictive biomarker for adjuvant chemotherapy with tegafur/uracil in stage I lung adenocarcinomas.

Rintaro Noro, Kazufumi Honda, Kengo Nagashima, Noriko Motoi, Shinobu Kunugi, Jun Matsubayashi, Susumu Takeuchi, Hideaki Shiraishi, Tetsuya Okano, Ayumi Kashiro and 10 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cancer science, 2022. 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
0.7field-weighted citation impact, top 27% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
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 7 institutions in 3 countries.

Rintaro NoroDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4912-4138
Kazufumi HondaDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1321-5345
Kengo NagashimaResearch Center for Medical and Health Data Science, Keio University Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4529-9045
Noriko MotoiDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7098-3311
Shinobu KunugiDepartment of Analytic Human Pathology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Jun MatsubayashiDepartment of Anatomical Pathology, Tokyo Medical University, Tokyo, Japan.
Susumu TakeuchiDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Hideaki ShiraishiDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Tetsuya OkanoDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Ayumi KashiroDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Xue MengDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Yukihiro YoshidaDepartment of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan.
Shunichi WatanabeDepartment of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan.
Jitsuo UsudaDepartment of Thoracic Surgery, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Tatsuya InoueDepartment of Thoracic Surgery, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Huang WilberAbnova, Taipei City, Taiwan.
Norihiko IkedaDepartment of Surgery, Tokyo Medical University, Tokyo, Japan.
Masahiro SeikeDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Akihiko GemmaDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Kaoru KubotaDepartment of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Nippon Medical School · JPNational Cancer Research Institute · GBTokyo Medical University · JPTokyo National Hospital · JPBova (Taiwan) · TWKeio University Hospital · JPSaitama Cancer Center · JP

Funding

Japan Agency for Medical Research and Development (AMED) 17ck0106295h0001
6 · The paper itself

Abstract

Although adjuvant tegafur/uracil (UFT) is recommended for patients with completely resected stage I non-small-cell lung cancer (NSCLC) in Japan, only one-third of cases has received adjuvant chemotherapy (ADJ) according to real-world data. Therefore, robust predictive biomarkers for selecting ADJ or observation (OBS) without ADJ are needed. Patients who underwent complete resection of stage I lung adenocarcinoma with or without adjuvant UFT were enrolled. The status of ACTN4 gene amplification was analyzed by FISH. Statistical analyses to determine whether the status of ACTN4 gene amplification affected recurrence-free survival (RFS) were carried out. Formalin-fixed, paraffin-embedded samples from 1136 lung adenocarcinomas were submitted for analysis of ACTN4 gene amplification. Ninety-nine (8.9%) of 1114 cases were positive for ACTN4 gene amplification. In the subgroup analysis of patients aged 65 years or older, the ADJ group had better RFS than the OBS group in the ACTN4-positive cohort (hazard ratio [HR], 0.084, 95% confidence interval [CI], 0.009-0.806; P = .032). The difference in RFS between the ADJ group and the OBS group was not significant in ACTN4-negative cases (all ages: HR, 1.214; 95% CI, 0.848-1.738; P = .289). Analyses of ACTN4 gene amplification contributed to the decision regarding postoperative ADJ for stage I lung adenocarcinomas, preventing recurrence, improving the quality of medical care, preventing the unnecessary side-effects of ADJ, and saving medical costs.

Indexed as

ActininAdenocarcinoma of LungAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorChemotherapy, AdjuvantFemaleGene AmplificationHumansJapanLung NeoplasmsMaleMiddle AgedNeoplasm StagingRetrospective StudiesTegafurActininACTN4 protein, humanBiomarkers, TumorTegafurUracilACTN4 gene amplificationadjuvant chemotherapylung adenocarcinomarecurrence-free survivaltegafur-uracil

Identifiers

PMID34845792
PMCPMC8898703
OpenAlexW3215090994

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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.