Evidence map›Paper›PMID 37864465›Full record

ArticleMolecular oncology2024

NOTCH1 and CREBBP co-mutations negatively affect the benefit of adjuvant therapy in completely resected EGFR-mutated NSCLC: translational research of phase III IMPACT study.

Satoshi Ikeda, Masahiro Tsuboi, Kazuko Sakai, Toshihiro Misumi, Hiroaki Akamatsu, Hiroyasu Shoda, Noriaki Sakakura, Atsushi Nakamura, Yasuhisa Ohde, Hidetoshi Hayashi and 22 more

Abstract read
In one paragraph

Article in Molecular oncology, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. 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

32 authors.

Satoshi IkedaDepartment of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan.ORCID 0000-0001-5203-7911
Masahiro TsuboiDivision of Thoracic Surgery, National Cancer Center Hospital East, Kashiwa, Japan.
Kazuko SakaiDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Toshihiro MisumiDepartment of Data Science, National Cancer Center Hospital East, Kashiwa, Japan.
Hiroaki AkamatsuInternal Medicine III, Wakayama Medical University, Japan.
Hiroyasu ShodaDepartment of Respiratory Medicine, Hiroshima Citizens Hospital, Japan.
Noriaki SakakuraDepartment of Thoracic Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
Atsushi NakamuraDepartment of Pulmonary Medicine, Sendai Kousei Hospital, Japan.
Yasuhisa OhdeDivision of Thoracic Surgery, Shizuoka Cancer Center, Sunto-gun, Japan.
Hidetoshi HayashiDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kyoichi OkishioDepartment of Thoracic Oncology, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Morihito OkadaDepartment of Surgical Oncology, Hiroshima University, Japan.
Ichiro YoshinoDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Japan.
Jiro OkamiDepartment of General Thoracic Surgery, Osaka International Cancer Institute, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Norihiko IkedaDepartment of Surgery, Tokyo Medical University, Shinjuku-ku, Japan.
Masayuki TanahashiDivision of Thoracic Surgery, Respiratory Disease Center, Seirei Mikatahara General Hospital, Hamamatsu, Japan.
Yuichi TamboDepartment of Respiratory Medicine, Kanazawa University Hospital, Japan.
Haruhiro SaitoDepartment of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.
Shinichi ToyookaDepartment of General Thoracic Surgery, Okayama University Graduate School of Medicine, Japan.
Hidetoshi InokawaDepartment of Thoracic Surgery, Yamaguchi-Ube Medical Center, Japan.
Toyofumi Chen-YoshikawaDepartment of Thoracic Surgery, Nagoya University Graduate School of Medicine, Japan.
Toshihide YokoyamaDepartment of Respiratory Medicine, Kurashiki Central Hospital, Japan.
Tatsuro OkamotoDepartment of Thoracic Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.
Noriko YanagitaniDepartment of Thoracic Medical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Koto-ku, Japan.
Masahide OkiDepartment of Respiratory Medicine, National Hospital Organization Nagoya Medical Center, Japan.
Makoto TakahamaDepartment of General Thoracic Surgery, Osaka City General Hospital, Japan.
Kenji SawaDepartment of Clinical Oncology, Osaka Metropolitan University Graduate School of Medicine, Japan.
Hirohito TadaDepartment of Thoracic Surgery, Suita Tokushukai Hospital, Japan.
Kazuhiko NakagawaDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Tetsuya MitsudomiDivision of Thoracic Surgery, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kazuto NishioDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.ORCID 0000-0002-8275-0846

Funding

AstraZeneca KK
6 · The paper itself

Abstract

The phase III IMPACT study (UMIN000044738) compared adjuvant gefitinib with cisplatin plus vinorelbine (cis/vin) in completely resected epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC). Although the primary endpoint of disease-free survival (DFS) was not met, we searched for molecular predictors of adjuvant gefitinib efficacy. Of 234 patients enrolled in the IMPACT study, 202 patients were analyzed for 409 cancer-related gene mutations and tumor mutation burden using resected lung cancer specimens. Frequent somatic mutations included tumor protein p53 (TP53; 58.4%), CUB and Sushi multiple domains 3 (CSMD3; 11.8%), and NOTCH1 (9.9%). Multivariate analysis showed that NOTCH1 co-mutation was a significant poor prognostic factor for overall survival (OS) in the gefitinib group and cAMP response element binding protein (CREBBP) co-mutation for DFS and OS in the cis/vin group. In patients with NOTCH1 co-mutations, gefitinib group had a shorter OS than cis/vin group (Hazard ratio 5.49, 95% CI 1.07-28.00), with a significant interaction (P for interaction = 0.039). In patients with CREBBP co-mutations, the gefitinib group had a longer DFS than the cis/vin group, with a significant interaction (P for interaction = 0.058). In completely resected EGFR-mutated NSCLC, NOTCH1 and CREBBP mutations might predict poor outcome in patients treated with gefitinib and cis/vin, respectively.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsCisplatinCREB-Binding ProteinCyclic AMP Response Element-Binding ProteinErbB ReceptorsGefitinibHumansMutationProtein Kinase InhibitorsReceptor, Notch1Translational Research, BiomedicalVinorelbineCisplatinCREB-Binding ProteinCREBBP protein, humanCyclic AMP Response Element-Binding ProteinEGFR protein, humanErbB ReceptorsGefitinibNOTCH1 protein, humanProtein Kinase InhibitorsReceptor, Notch1Vinorelbineadjuvant therapyearly-stageepidermal growth factor receptornon-small cell lung cancertyrosine kinase inhibitor

Identifiers

PMID37864465
PMCPMC10850799

What Socratic 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 Socratic graph.