Evidence map›Paper›PMID 26744648›Full record

ArticleRespiratory medicine case reports2015

Unexpected responses to EGFR inhibition in NSCLC.

Giulia M Stella, Claudio Valizia, Michele Zorzetto, Simona Inghilleri, Adele Valentini, Roberto Dore, Sara Colombo, Francesco Valentino, Giulio Orlandoni, Patrizia Morbini

Open access · goldAbstract readCase Reports
In one paragraph

Article in Respiratory medicine case reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

10 authors at 3 institutions in 1 country.

Giulia M StellaDepartment of Molecular Medicine, Laboratory of Biochemistry and Genetics, Pneumology Unit, University and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Claudio ValiziaDepartment of Molecular Medicine, Laboratory of Biochemistry and Genetics, Pneumology Unit, University and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Michele ZorzettoDepartment of Molecular Medicine, Laboratory of Biochemistry and Genetics, Pneumology Unit, University and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Simona InghilleriDepartment of Molecular Medicine, Laboratory of Biochemistry and Genetics, Pneumology Unit, University and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Adele ValentiniInstitute of Radiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Roberto DoreInstitute of Radiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Sara ColomboDepartment of Hemato-oncology, Radiation Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Francesco ValentinoDepartment of Hemato-oncology, Medical Oncology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Giulio OrlandoniCardiothoracic Surgery Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Patrizia MorbiniDepartment of Molecular Medicine, Section of Pathology, University of Pavia and Foundation IRCCS Policlinico S. Matteo, Pavia, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITPoliclinico San Matteo Fondazione · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of activating mutations of the epidermal growth factor receptor (EGFR)-gene identifies a distinct and clinically relevant molecular subset of non-small-cell lung cancer. It is now well demonstrated that EGFR tyrosine kinase inhibitors (TKIs) gefitinib and erlotinib are superior to standard chemotherapy in this subset of tumors. Nevertheless, in many cases, responses are not durable and last for 6-12 months due to the occurrence of secondary or acquired resistance. Here we present three cases of EGFR-mutant lung adenocarcinomas (ADC), that showed an unexpected response to anti-EGFR small molecules. The first patient presented a continued 89 month-long response to erlotinib in a tumor recurred after surgery and conventional chemotherapy. In the other cases, subclinically persistent tumor in the lung tissue was documented histologically in lung resections performed after partial response to TKI treatment. The persistence of interstitial and endolymphatic tumor cells after TKI treatment might explain the common observation of tumor relapse after TKI discontinuation, and sustain the decision to continue treatment in responsive patients as in our first case.

Indexed as

Actionable markersCancer geneticsTargeted therapy

Identifiers

PMID26744648
PMCPMC4681892
OpenAlexW1931557976

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.