Evidence map›Paper›PMID 28167203›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2017

ERBB2-Mutated Metastatic Non-Small Cell Lung Cancer: Response and Resistance to Targeted Therapies.

Jody C Chuang, Henning Stehr, Ying Liang, Millie Das, Jane Huang, Maximilian Diehn, Heather A Wakelee, Joel W Neal

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 92 citations in OpenAlex.

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  16. Management of Combined Therapy (Ceritinib,Life (Basel, Switzerland) · 2022
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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 5 institutions in 2 countries.

Jody C ChuangDivision of Hematology and Oncology, Stanford Hospital and Clinics, Stanford, California.
Henning StehrStanford Cancer Institute, Stanford University, Stanford, California.
Ying LiangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, People's Republic of China.
Millie DasDepartment of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California; Palo Alto Veterans Administration Health Care System, Palo Alto, California.
Jane HuangDepartment of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California.
Maximilian DiehnStanford Cancer Institute, Stanford University, Stanford, California; Department of Radiation Oncology, Stanford University, Stanford, California.
Heather A WakeleeDepartment of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California.
Joel W NealDepartment of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California. Electronic address: jwneal@stanford.edu.
Stanford University · USStanford Medicine · USStanford Health Care · USSun Yat-sen University · CNVA Palo Alto Health Care System · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
NCI NIH HHS P30 CA124435
6 · The paper itself

Abstract

introductionErb-b2 receptor tyrosine kinase 2 gene (ERBB2) (also called HER2) has long been recognized as an oncogenic driver in some breast and gastroesophageal cancers in which amplification of this gene confers sensitivity to treatment with Erb-b2 receptor tyrosine kinase 2 (ERBB2)-directed agents. More recently, somatic mutations in ERBB2 have been reported in 1% to 2% of patients with lung adenocarcinoma. Previous case series have suggested clinical tumor responses using anti-ERBB2 small molecules and antibody therapies.

methodsHere we report the outcomes of nine patients with metastatic lung adenocarcinoma with ERBB2 mutations being treated with ERBB2-targeted therapies.

resultsFour of the nine patients had response to targeted therapies, with durations of response ranging from 3 to 10 months. We identified a de novo phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene (PIK3CA) mutation and ERBB2 copy number gain as potential resistance mechanisms.

conclusionsWe showed patients with ERBB2-mutated lung adenocarcinoma can respond to targeted therapies, and we identified potential resistance mechanisms upon progression to targeted therapies.

Indexed as

Genes, erbB-2AdenocarcinomaAdo-Trastuzumab EmtansineAdultAfatinibAgedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungClass I Phosphatidylinositol 3-KinasesDocetaxelDrug Resistance, NeoplasmFemaleGene DosageHumansLung NeoplasmsMaleAdo-Trastuzumab EmtansineAfatinibClass I Phosphatidylinositol 3-KinasesDocetaxelMaytansinePaclitaxelPIK3CA protein, humanQuinazolinesTaxoidsTrastuzumabVinblastineVinorelbineAfatinibERBB2HER2Targeted therapyTrastuzumab

Identifiers

PMID28167203
PMCPMC5402884
OpenAlexW2585022678

What OpenQuestion holds

Textmetadata
LicenceTDM
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.