Evidence map›Paper›PMID 35430596›Full record

Observational studyScientific reports2022

Observational study of rebiopsy in EGFR-TKI-resistant patients with EGFR mutation-positive advanced NSCLC.

Kenichi Koyama, Satoru Miura, Satoshi Watanabe, Satoshi Shoji, Jun Koshio, Yoshiki Hayashi, Daisuke Ishikawa, Ko Sato, Takao Miyabayashi, Masaaki Okajima and 10 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 11 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

20 authors at 10 institutions in 1 country.

Kenichi KoyamaDepartment of Internal Medicine, Niigata Cancer Center Hospital, 2-15-3, Kawagishi-cho, Chuo-ku, Niigata city, 951-8566, Japan.
Satoru MiuraDepartment of Internal Medicine, Niigata Cancer Center Hospital, 2-15-3, Kawagishi-cho, Chuo-ku, Niigata city, 951-8566, Japan. miusat1118@niigata-cc.jp.
Satoshi WatanabeDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachidori, Chuouku, Niigata, 951-8510, Japan. satoshi7@med.niigata-u.ac.jp.
Satoshi ShojiDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachidori, Chuouku, Niigata, 951-8510, Japan.
Jun KoshioDepartment of Respiratory Medicine, Nagaoka Red Cross Hospital, Niigata, Japan.
Yoshiki HayashiDepartment of Respiratory Medicine, Nagaoka Chuo General Hospital, Niigata, Japan.
Daisuke IshikawaDepartment of Respiratory Medicine, Niigata Prefectural Central Hospital, Niigata, Japan.
Ko SatoDepartment of Respiratory Medicine, Niigata Prefectural Central Hospital, Niigata, Japan.
Takao MiyabayashiDepartment of Respiratory Medicine, Niigata City General Hospital, Niigata, Japan.
Masaaki OkajimaDepartment of Respiratory Medicine, Saiseikai Niigata Hospital, Niigata, Japan.
Takeshi OtaDepartment of Respiratory Medicine, Shibata Hospital - Niigata Prefectural Hospital, Niigata, Japan.
Tomohiro TanakaDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachidori, Chuouku, Niigata, 951-8510, Japan.
Naoya MatsumotoDepartment of Respiratory Medicine, Nishi Niigata Chuo Hospital, Niigata, Japan.
Hideyuki KuriyamaDepartment of Respiratory Medicine, Niigata Medical Center, Niigata, Japan.
Tetsuya AbeDepartment of Respiratory Medicine, Niigata City General Hospital, Niigata, Japan.
Koichiro NozakiDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachidori, Chuouku, Niigata, 951-8510, Japan.
Kosuke IchikawaDepartment of Respiratory Medicine, Saiseikai Niigata Hospital, Niigata, Japan.
Rie KondoDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachidori, Chuouku, Niigata, 951-8510, Japan.
Hiroshi TanakaDepartment of Internal Medicine, Niigata Cancer Center Hospital, 2-15-3, Kawagishi-cho, Chuo-ku, Niigata city, 951-8566, Japan.
Toshiaki KikuchiDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachidori, Chuouku, Niigata, 951-8510, Japan.
Niigata University · JPNiigata Cancer Center Hospital · JPNiigata City General Hospital · JPNiigata Prefectural Central Hospital · JPNiigata University Medical and Dental Hospital · JPSaiseikai Niigata Daini Hospital · JPNagaoka Red Cross Hospital · JPNagara Medical Center · JPNiigata Prefectural Shibata Hospital · JPNishi Niigata Chuo National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of acquired resistance mutations has been essential in non-small-cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) active mutations. Rebiopsy plays a pivotal role in selecting the optimal treatment for patients who develop resistance to initial EGFR-tyrosine kinase inhibitors (EGFR-TKIs). This multicenter, observational study was conducted to investigate the details of rebiopsy in Japanese clinical practice. The primary endpoints were the implementation rate of rebiopsy and the concordance rate for T790M mutation detection between histological and cytological specimens using the cobas EGFR Mutation Test, version 2. One hundred ninety-four patients with EGFR-mutant NSCLC were enrolled, and 120 patients developed acquired resistance to EGFR-TKIs. The median age was 68 years (range 20-87), and 52.5% of the patients were women. Rebiopsy was performed in 109 patients, and the implementation rate of rebiopsy was 90.8%. The success rates of rebiopsy in the total, histology, cytology and liquid biopsy populations were 67.9%, 81.3%, 66.7% and 43.8%, respectively. The positive percent agreement and the negative percent agreement in the detection of the T790M mutation between the histological and cytological specimens were both 90.9%. Obtaining histological or cytological tissue samples at rebiopsy may contribute to improving the detection rate of the T790M mutation (trial registration number: UMIN000026019).

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedAged, 80 and overBiopsyDrug Resistance, NeoplasmErbB ReceptorsFemaleHumansMaleMiddle AgedMutationProtein Kinase InhibitorsYoung AdultEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitors

Identifiers

PMID35430596
PMCPMC9013397
OpenAlexW4226094392

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.