Defining aggressive or early progressing nononcogene-addicted non-small-cell lung cancer: a separate disease entity?


Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
Apr 2019
Historique:
pubmed: 14 2 2019
medline: 20 8 2019
entrez: 14 2 2019
Statut: ppublish

Résumé

A substantial proportion of patients with nononcogene-addicted non-small-cell lung cancer (NSCLC) has 'aggressive disease', as reflected in short time to progression or lack of disease control with initial platinum-based chemotherapy. Recently, clinical correlates of aggressive disease behavior during first-line therapy have been shown to predict greater benefit from addition of nintedanib to second-line docetaxel in adenocarcinoma NSCLC. Positive predictive effects of aggressive disease have since been reported with other anti-angiogenic agents (ramucirumab and bevacizumab), while such features may negatively impact on outcomes with nivolumab in nonsquamous NSCLC with low PD-L1 expression. Based on a review of the clinical data, we recommend aggressive nonsquamous NSCLC should be defined by progression within <6-9 months of first-line treatment initiation.

Identifiants

pubmed: 30758227
doi: 10.2217/fon-2018-0948
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antibodies, Monoclonal, Humanized 0
Indoles 0
Docetaxel 15H5577CQD
Bevacizumab 2S9ZZM9Q9V
nintedanib G6HRD2P839

Types de publication

Journal Article Review

Langues

eng

Pagination

1363-1383

Auteurs

Martin Reck (M)

Department of Thoracic Oncology, Lung Clinic Grosshansdorf, Member of the German Center for Lung Research (DZL), Grosshansdorf, Germany.

Keith M Kerr (KM)

Department of Pathology, Aberdeen University Medical School, Aberdeen Royal Infirmary, Aberdeen, Scotland.

Christian Grohé (C)

Department of Respiratory Diseases, Evangelische Lungenklinik Berlin, Lindenberger Weg 27, Berlin, Germany.

Christian Manegold (C)

Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.

Nick Pavlakis (N)

Department of Medical Oncology, Royal North Shore Hospital (Sydney University), Reserve Road, St Leonards 2065, New South Wales, Australia.

Luis Paz-Ares (L)

Medical Oncology Department, University Hospital 12 de Octubre, Complutense University, CNIO & CiberOnc, Madrid, Spain.

Rudolf M Huber (RM)

Division of Respiratory Medicine & Thoracic Oncology, Ludwig Maximilians University of Munich, & Thoracic Oncology Centre Munich, Member of the German Center for Lung Research (DZL CPC-M) Munich, Germany.

Sanjay Popat (S)

Department of Medicine, Royal Marsden Hospital NHS Foundation Trust, London, UK.

Nick Thatcher (N)

Department of Medical Oncology, Christie Hospital NHS Trust, Wilmslow Road, Manchester, UK.

Keunchil Park (K)

Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Frank Hilberg (F)

Boehringer Ingelheim RCV GmbH & Co. KG, A-1121, Vienna, Austria.

José Barrueco (J)

Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, Connecticut, CT 06877, USA.

Rolf Kaiser (R)

Boehringer Ingelheim Pharma GmbH & Co, KG, Germany & Institute of Pharmacology, Johannes Gutenberg-University Mainz, Germany.

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Classifications MeSH