Evidence map›Paper›PMID 32129931›Full record

Observational studyThoracic cancer2020

Osimertinib, a third-generation EGFR tyrosine kinase inhibitor: A retrospective multicenter study of its real-world efficacy and safety in advanced/recurrent non-small cell lung carcinoma.

Takayuki Kishikawa, Takashi Kasai, Masahiko Okada, Ichiro Nakachi, Sayo Soda, Ryo Arai, Ayako Takigami, Masafumi Sata

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Observational
  3. Modular Vinyl Phosphonamidates for Cysteine-Directed Protein Targeting.Journal of the American Chemical Society · 2026
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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

8 authors at 4 institutions in 1 country.

Takayuki KishikawaDepartment of Respiratory Medicine, Tochigi Cancer Center, Utsunomiya, Japan.ORCID 0000-0002-8957-4814
Takashi KasaiDepartment of Respiratory Medicine, Tochigi Cancer Center, Utsunomiya, Japan.
Masahiko OkadaPulmonary Division, Department Internal Medicine, Saiseikai Utsunomiya Hospital, Utsunomiya, Japan.
Ichiro NakachiPulmonary Division, Department Internal Medicine, Saiseikai Utsunomiya Hospital, Utsunomiya, Japan.
Sayo SodaDepartment of Pulmonary Medicine and Clinical Immunology, Dokkyo Medical University School of Medicine, Shimotuga-Gun, Japan.
Ryo AraiDepartment of Pulmonary Medicine and Clinical Immunology, Dokkyo Medical University School of Medicine, Shimotuga-Gun, Japan.
Ayako TakigamiDivision of Pulmonary Medicine, Department of Medicine, Jichi Medical University Hospital, Shimotsuke-City, Japan.
Masafumi SataDivision of Pulmonary Medicine, Department of Medicine, Jichi Medical University Hospital, Shimotsuke-City, Japan.
Dokkyo Medical University · JPJichi Medical University · JPSaiseikai Utsunomiya hospital · JPTochigi Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsimertinib is recommended for T790M mutation-positive advanced non-small cell lung cancer (NSCLC) resistant to first- and second-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs). Recently, some reports exist on the real-world use of osimertinib; however, reports involving third/later-line use are few. Hence, this study was conducted to evaluate the efficacy and safety of osimertinib used in various treatment lines for T790M-positive NSCLC patients.

methodsThis retrospective, observational, multicenter study included T790M-positive advanced/recurrent NSCLC patients treated with osimertinib from May 2016 to March 2018. The clinical characteristics, efficacy, and adverse events were retrospectively investigated. The Kaplan-Meier method was used to analyze progression-free survival (PFS) and overall survival (OS). PFS-associated clinical characteristics were evaluated using the Cox proportional hazards model.

resultsThe objective response rate (ORR) and disease control rate (DCR) were 60.7% and 91.1%, respectively; the median PFS was 11.0 months. There were no significant differences in the median PFS for patients treated with osimertinib as second-line and third-/later-line (14.5 vs. 11.0 months respectively, P = 0.327). Analysis using the Cox proportional hazards model for clinical features affecting PFS also revealed no significant factors. Adverse events of grade ≥ 3 were reported in 15 patients (26.8%); the most common were anemia (n = 3) and cutaneous toxicity (n = 3). Grade 4 neutropenia was observed in one patient; any-grade pneumonitis was observed in six patients (10.7%), including one with grade 3 pneumonitis.

conclusionsOsimertinib demonstrated efficacy even when administered as third-/later-line treatment to NSCLC patients. Osimertinib-related pneumonitis was observed more frequently than previously reported. KEY POINTS: Significant findings of the study Osimertinib shows efficacy even as later-line treatment in T790M mutation-positive NSCLC patients previously treated with EGFR-TKIs. However, the incidence of ≥ grade 3 adverse events, especially pneumonitis, was higher than that previously reported by other studies. What this study adds Osimertinib was approved for previously EGFR-TKI-treated EGFR T790M-positive NSCLC. With the increasing frequency of its use as first-line treatment, this study provides valuable evidence for the efficacy and safety of osimertinib for previously EGFR-TKI-treated NSCLC.

Indexed as

AcrylamidesAdenocarcinoma of LungAdultAgedAged, 80 and overAniline CompoundsCarcinoma, Large CellCarcinoma, Non-Small-Cell LungErbB ReceptorsFemaleFollow-Up StudiesHumansIndolesLung NeoplasmsMaleMiddle AgedAcrylamidesAniline CompoundsEGFR protein, humanErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidinesEpidermal growth factor receptor T790M mutationnon-small cell lung cancerosimertinibtyrosine kinase inhibitor

Identifiers

PMID32129931
PMCPMC7113046
OpenAlexW3010280371

What OpenQuestion holds

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LicenceCC BY
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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.