Evidence map›Paper›PMID 39255996›Full record

Observational studyJapanese journal of clinical oncology2024

The effect of epidermal growth factor receptor mutation on adjuvant chemotherapy with tegafur/uracil for patients with completely resected, non-lymph node metastatic non-small cell lung cancer (> 2 cm): a multicenter, retrospective, observational study as exploratory analysis of the CSPOR-LC03 study.

Tomohiro Miyoshi, Keiju Aokage, Shun-Ichi Watanabe, Hiroyuki Ito, Noriaki Sakakura, Mingyon Mun, Motohiro Yamashita, Yasuhisa Ohde, Tadashi Aoki, Wataru Nishio and 2 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Japanese journal of clinical 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. Review
  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

12 authors.

Tomohiro MiyoshiDivision of Thoracic Surgery, Department of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.ORCID 0000-0002-6311-0691
Keiju AokageDivision of Thoracic Surgery, Department of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.
Shun-Ichi WatanabeDivision of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan.
Hiroyuki ItoDepartment of Thoracic Surgery, Kanagawa Cancer Center, Kanagawa, Japan.
Noriaki SakakuraDepartment of Thoracic Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
Mingyon MunDepartment of Thoracic Surgical Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Motohiro YamashitaDepartment of Thoracic Surgery, Shikoku Cancer Center, Ehime, Japan.
Yasuhisa OhdeDivision of Thoracic Surgery, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Tadashi AokiDepartment of Chest Surgery, Niigata Cancer Center Hospital, Niigata, Japan.
Wataru NishioDepartment of Chest Surgery, Hyogo Cancer Center, Hyogo, Japan.
Masataka TaguriDepartment of Health Data Science, Tokyo Medical University, Tokyo, Japan.
Masahiro TsuboiDivision of Thoracic Surgery, Department of Thoracic Oncology, National Cancer Center Hospital East, Chiba, Japan.

Funding

AstraZeneca KK ESR-21-21264
6 · The paper itself

Abstract

backgroundThe use of adjuvant osimertinib for epidermal growth factor receptor (EGFR) mutants is expected to expand to earlier stage I in the future, potentially competing with the current standard of care, oral tegafur/uracil (UFT), in Japan. However, the effect of EGFR mutation status on the therapeutic effect of UFT remains unclear. This study was conducted as an exploratory analysis of a retrospective observational study that investigated the real-world data of postoperative adjuvant chemotherapy in Japan (CSPOR-LC03).

methodsBetween 2008 and 2013, 1812 patients with completely resected adenocarcinoma diagnosed as pathologic stage I (T1 > 2 cm, TNM classification, sixth edition) who have maintained organ function, and no history of other cancers were included. The primary endpoint was the 5-year disease-free survival (DFS) rate, and we compared this rate between four groups classified based on the administration of adjuvant UFT and EGFR mutation status.

resultsOf the 933 (51%) patients with EGFR mutations, 394 underwent adjuvant UFT therapy. Of the 879 (49%) patients without EGFR mutations, 393 underwent adjuvant UFT therapy. The 5-year DFS of UFT+/EGFR+ and UFT-/EGFR+ patients were 82.0 and 87.1%, respectively, and those of UFT+/EGFR- and UFT-/EGFR- patients were 80.0 and 86.9%, respectively. DFS was significantly worse in the UFT+ group than in the UFT- group (P = 0.015). Adjuvant UFT therapy was not an independent prognostic factor for DFS, regardless of the EGFR mutation status.

conclusionIn pathologic stage I (>2 cm) lung adenocarcinomas with EGFR mutation, the survival benefit of adjuvant UFT was not observed.

Indexed as

Carcinoma, Non-Small-Cell LungErbB ReceptorsLung NeoplasmsMutationTegafurUracilAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantDisease-Free SurvivalFemaleHumansJapanMaleEGFR protein, humanErbB ReceptorsTegafurUraciladjuvant chemotherapyepidermal growth factor receptorlung cancertegafur/uracil

Identifiers

PMID39255996
PMCPMC11532619

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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.