Evidence map›Paper›PMID 29662657›Full record

ArticleOncotarget2018

5'-nucleotidase cN-II emerges as a new predictive biomarker of response to gemcitabine/platinum combination chemotherapy in non-small cell lung cancer.

Francesca Toffalorio, Mariacarmela Santarpia, Davide Radice, Christopher Adrian Jaramillo, Gianluca Spitaleri, Michela Manzotti, Chiara Catania, Lars Petter Jordheim, Giuseppe Pelosi, Godefridus J Peters and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

16 authors at 9 institutions in 3 countries.

Francesca ToffalorioMedical Oncology Unit of Respiratory Tract and Sarcomas, New Drugs Development Division, European Institute of Oncology, Milan, Italy.
Mariacarmela SantarpiaMedical Oncology Unit of Respiratory Tract and Sarcomas, New Drugs Development Division, European Institute of Oncology, Milan, Italy.
Davide RadiceEpidemiology and Biostatistics Division, European Institute of Oncology, Milan, Italy.
Christopher Adrian JaramilloDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Gianluca SpitaleriMedical Oncology Unit of Respiratory Tract and Sarcomas, New Drugs Development Division, European Institute of Oncology, Milan, Italy.
Michela ManzottiDivision of Pathology and Laboratory Medicine, European Institute of Oncology, Milan, Italy.
Chiara CataniaMedical Oncology Unit of Respiratory Tract and Sarcomas, New Drugs Development Division, European Institute of Oncology, Milan, Italy.
Lars Petter JordheimCentre de Recherche en Cancérologie de Lyon, INSERM 1052/CNRS UMR 5286, Lyon, France.
Giuseppe PelosiDepartment of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Godefridus J PetersDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Carmelo TibaldiDivision of Oncology, Department of Oncology, S. Luca Hospital, Lucca, Italy.
Niccola FunelCNR-Nano, Institute of Nanoscience and Nanotechnology, Pisa, Italy.
Lorenzo SpaggiariThoracic Surgery Division, European Institute of Oncology, Milan, Italy.
Filippo de BraudDepartment of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Tommaso De PasMedical Oncology Unit of Respiratory Tract and Sarcomas, New Drugs Development Division, European Institute of Oncology, Milan, Italy.
Elisa GiovannettiDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
European Institute of Oncology · ITAmsterdam UMC Location VUmc · NLCentre de Recherche en Cancérologie de Lyon · FRIstituto Nanoscienze · ITMultiMedica · ITRoche (Italy) · ITUniversity of Messina · ITUniversity of Milan · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A number of pharmacogenetic studies have been carried out in non-small-cell lung cancer (NSCLC) to identify and characterize genes involved in chemotherapy activity. However, the results obtained so far are controversial and no reliable biomarker is currently used to predict clinical benefit from platinum-based chemotherapy, which represents the cornerstone of treatment of advanced NSCLC. This study investigated the expression levels of ERCC1 and of six genes (RRM1, RRM2, hENT1, dCK, cN-II and CDA) involved in gemcitabine metabolism in locally/advanced NSCLC patients treated with gemcitabine/platinum combination. Gene expression was assessed by quantitative-PCR in laser-microdissected specimens and correlated with tumor response. Frequency distribution of responses above and below the median expression level of biomarkers was compared using a two-sided Fisher's test. 5'-nucleotidase (cN-II) was the only gene differently expressed (

Indexed as

gemcitabinelung cancernucleotidasepharmacogeneticsresponse

Identifiers

PMID29662657
PMCPMC5893252
OpenAlexW2793457196

What OpenQuestion holds

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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.