Evidence map›Paper›PMID 29435365›Full record

ArticleESMO open2016

Novel active agents in patients with advanced NSCLC without driver mutations who have progressed after first-line chemotherapy.

Christian Manegold, Alex Adjei, Federico Bussolino, Federico Cappuzzo, Lucio Crino, Rafal Dziadziuszko, David Ettinger, Dean Fennell, Keith Kerr, Thierry Le Chevalier and 12 more

Abstract read
In one paragraph

Article in ESMO open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

22 authors.

Christian ManegoldMedical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany. Electronic address: prof.manegold@t-online.de.
Alex AdjeiDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, New York, USA.
Federico BussolinoDepartment of Oncology, University of Turin, Turin and Candiolo Cancer Institute, Candiolo, Italy.
Federico CappuzzoMedical Oncology Department, Istituto Toscano Tumori, Livorno, Italy.
Lucio CrinoMedical Oncology Department, Perugia University Medical School, Perugia, Italy.
Rafal DziadziuszkoDepartment of Oncology and Radiotherapy, Medical University of Gdansk, Gdansk, Poland.
David EttingerSidney Kimmel Comprehensive Cancer Center, Johns Hopkins Medicine, Baltimore, Maryland, USA.
Dean FennellDepartment of Oncology, University of Leicester & Leicester University Hospitals, Leicester, UK.
Keith KerrDepartment of Pathology, Aberdeen University Medical School, Aberdeen, UK.
Thierry Le ChevalierDepartment of Medicine, Gustave Roussy University Hospital, Villejuif, France.
Natasha LeighlCancer Clinical Research Unit (CCRU), Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Mauro PapottiDepartment of Oncology, University of Turin, Turin, Italy.
Luis Paz-AresServicio de Oncología Médica, Doce de Octubre University Hospital, Madrid, Spain.
Maurice PérolDépartement de Cancérologie Médicale, Centre Léon Bérard, Lyon, France.
Solange PetersDepartment of Oncology, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
Robert PirkerDepartment of Medicine I, Medical University of Vienna, Vienna, Austria.
Elisabeth QuoixPulmonology Department, University Hospital, Strasbourg, France.
Martin ReckDepartment of Thoracic Oncology, Airway Research Center North (ARCN), member of the German Center for Lung Research (DZL), Lung Clinic Grosshansdorf, Grosshansdorf, Germany.
Egbert SmitDepartment of Pulmonary Diseases, VU University Medical Centre, Amsterdam, The Netherlands; Department of Thoracic Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Everett VokesDepartment of Medicine, University of Chicago Medicine and Biological Sciences, Chicago, Illinois, USA.
Nico van ZandwijkAsbestos Diseases Research Institute, University of Sydney, Sydney, New South Wales, Australia.
Caicun ZhouDepartment of Oncology, Shanghai Pulmonary Hospital, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the efficacy of a number of first-line treatments, most patients with advanced-stage non-small cell lung cancer (NSCLC) experience disease progression that warrants further treatment. In this review, we examine the role of novel active agents for patients who progress after first-line therapy and who are not candidates for targeted therapies. More therapeutic options are needed for the management of patients with NSCLC after failure of first-line chemotherapy. A PubMed search was performed for articles from January 2012 to May 2015 using the keywords NSCLC, antiangiogenic, immunotherapy, second-line, novel therapies and English language articles only. Relevant papers were reviewed; papers outside that period were considered on a case-by-case basis. A search of oncology congresses was performed to identify relevant abstracts over this period. In recent years, antiangiogenic agents and immune checkpoint inhibitors have been added to our armamentarium to treat patients with advanced NSCLC who have progressed on first-line chemotherapy. These include nintedanib, a triple angiokinase inhibitor; ramucirumab, a vascular endothelial growth factor receptor-2 antibody; and nivolumab, pembrolizumab and atezolizumab, just three of a growing list of antibodies targeting the programmed death receptor-1 (PD-1)/PD ligand-1 pathway. Predictive and prognostic factors in NSCLC treatment will help to optimise treatment with these novel agents. The approval of new treatments for patients with NSCLC after the failure of first-line chemotherapy has increased options after a decade of few advances, and holds promise for future evolution of the management of NSCLC.

Indexed as

AntiangiogenesisImmune checkpoint inhibitorsNintedanibPrognostic factorsRamucirumab

Identifiers

PMID29435365
PMCPMC5729303

What OpenQuestion holds

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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.