Evidence map›Paper›PMID 33080698›Full record

ArticleMedicine2020

Poor effect of osimertinib on EGFR exon 20 insertion-positive lung adenocarcinoma: A case report.

Yuji Inagaki, Akihiro Tamiya, Yoshinobu Matsuda, Kouji Azuma, Yuichi Adachi, Takatoshi Enomoto, Shunichi Kouno, Yoshihiko Taniguchi, Nobuhiko Saijo, Kyoichi Okishio and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 45% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 4 institutions in 7 countries.

Yuji InagakiDepartment of Internal Medicine.ORCID 0000-0002-2208-9478
Akihiro TamiyaDepartment of Internal Medicine.
Yoshinobu MatsudaDepartment of Psychosomatic Internal Medicine.
Kouji AzumaDepartment of Internal Medicine.
Yuichi AdachiDepartment of Internal Medicine.
Takatoshi EnomotoDepartment of Internal Medicine.
Shunichi KounoDepartment of Internal Medicine.
Yoshihiko TaniguchiDepartment of Internal Medicine.
Nobuhiko SaijoDepartment of Internal Medicine.
Kyoichi OkishioClinical Research Center, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Osaka, Japan.
Shinji AtagiClinical Research Center, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Osaka, Japan.
African Field Epidemiology Network · NGAstraZeneca (Brazil) · BRBoehringer Ingelheim (Egypt) · EGNational Kinki Chuo Hospital for Chest Disease · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe clinical efficacy of osimertinib for patients with lung adenocarcinoma harboring epidermal growth factor receptor (EGFR) exon 20 insertion mutations is unclear. Few case reports exist on the successful treatment of such tumors with osimertinib. We report a case wherein osimertinib administration had no effect in a patient with EGFR exon 20 insertion-positive lung adenocarcinoma. PATIENT CONCERNS: A 48-year-old never-smoking woman was referred to our hospital for chronic cough. Computed tomography (CT) and positron emission tomography-CT revealed a nodule in the right middle lobe, consolidation in the right upper lobe, multiple lymph node metastases, liver metastasis, and multiple bone metastases. DIAGNOSIS: On the basis of further examination using transbronchial lung biopsy, the patient was diagnosed with cT1N3M1 stage IVB lung adenocarcinoma. An EGFR exon 20 insertion, without any additional mutations, was identified.

interventionsDaily oral administration of 80 mg osimertinib was initiated to treat the EGFR exon 20 insertion-positive lung adenocarcinoma. OUTCOMES: Although the disease appeared to be stable 2.5 months after the administration of osimertinib, the tumor started to grow 3 months after administration, and carcinoembryonic antigen levels became higher than those before treatment. Thus, osimertinib was discontinued, and treatment with carboplatin as well as pemetrexed and bevacizumab was started, which the patient responded to.

conclusionEGFR exon 20 insertion mutations must be classified in more detail to assess the efficacy of EGFR tyrosine kinase inhibitors. Osimertinib doses that provide favorable therapeutic windows should be considered. Further clinical research is required to clarify the efficacy of osimertinib and other drugs for exon 20 insertion mutations.

Indexed as

Genes, erbB-1AcrylamidesAdenocarcinomaAniline CompoundsAntineoplastic AgentsFemaleHumansIndolesLung NeoplasmsMiddle AgedPyrimidinesTreatment FailureAcrylamidesAniline CompoundsAntineoplastic AgentsIndolesosimertinibPyrimidines

Identifiers

PMID33080698
PMCPMC7572000
OpenAlexW3094025159

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.