How I treat gastric adenocarcinoma.

gastric cancer gastro-esophageal cancer treatment algorithm

Journal

ESMO open
ISSN: 2059-7029
Titre abrégé: ESMO Open
Pays: England
ID NLM: 101690685

Informations de publication

Date de publication:
2019
Historique:
received: 29 03 2019
revised: 09 04 2019
accepted: 13 04 2019
entrez: 30 7 2019
pubmed: 30 7 2019
medline: 30 7 2019
Statut: epublish

Résumé

Gastric and gastro-oesophageal junction cancer (GC) represents a worldwide problem, this being the fifth most common malignancy. The fragility of patients with GC together with the aggressiveness of this tumour makes it as one of the most difficult neoplasias to manage. This article summarises the main strategies for treating patients with GC. Correct assessment of patients with GC requires a multidisciplinary evaluation and close follow-up. For patients with resectable tumours, perioperative chemotherapy should be always considered, especially in the neoadjuvant setting given its capacity for tumour downstaging and eradication of micro-metastases. In the metastatic setting, first-line and second-line treatment improve survival and quality of life in patients with GC. In this setting, only trastuzumab as first-line therapy in patients with human epidermal growth factor receptor 2 positive tumours and ramucirumab as second-line therapy have demonstrated a clear survival improvement. The lack of adequate biomarker selection and the intrinsic heterogeneity of these tumours have jeopardised the possible usefulness of many other targeted agents. Finally, when considering GC carcinogenesis as a multiple stepwise process from initial inflammation starting in the gastric epithelia, immune checkpoint inhibitors may improve the survival of these patients, although the optimal setting for their activity has yet to be fully elucidated.

Identifiants

pubmed: 31354966
doi: 10.1136/esmoopen-2019-000521
pii: S2059-7029(20)32613-2
pmc: PMC6615878
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

e000521

Déclaration de conflit d'intérêts

Competing interests: MA reports personal financial interest in form of scientific consultancy role for BMS, Servier and MSD. She has received honorarium for speaking issues from MSD, BMS, Lilly, Roche and Amgen; and has had travel expenses partially covered by Roche, Amgen and Lilly. JMM does not report personal financial interest. MD has received travel expenses partially covered by Ipsen, Lilly and Servier. SC reports personal financial interest in form of honorarium for speaking issues or travel expenses from Johnson&Johnson, Wyeth, Covidien and Roche. JT reports personal financial interest in form of scientific consultancy role for Array Biopharma, AstraZeneca, Bayer, BeiGene, Boehringer Ingelheim, Chugai, Genentech, Genmab A/S, Halozyme, Imugene Limited, Inflection Biosciences Limited, Ipsen, Kura Oncology, Lilly, MSD, Menarini, Merck Serono, Merrimack, Merus, Molecular Partners, Novartis, Peptomyc, Pfizer, Pharmacyclics, ProteoDesign SL, Rafael Pharmaceuticals, F. Hoffmann-La Roche Ltd, Sanofi, SeaGen, Seattle Genetics, Servier, Symphogen, Taiho, VCN Biosciences, Biocartis, Foundation Medicine, HalioDX SAS and Roche Diagnostics.

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Auteurs

Maria Alsina (M)

Medical Oncology, VHIO (Vall d'Hebron Institute of Oncology), University Hospital Vall d'Hebron, Barcelona, Spain; Facultat de Medicina, Universitat Autonoma de Barcelona, Bellaterra, Spain. Electronic address: malsina@vhio.net.

Josep Maria Miquel (JM)

Medical Oncology, VHIO (Vall d'Hebron Institute of Oncology), University Hospital Vall d'Hebron, Barcelona, Spain.

Marc Diez (M)

Medical Oncology, VHIO (Vall d'Hebron Institute of Oncology), University Hospital Vall d'Hebron, Barcelona, Spain.

Sandra Castro (S)

Surgery, Vall d'Hebron Hospital, Barcelona, Spain.

Josep Tabernero (J)

Medical Oncology, VHIO (Vall d'Hebron Institute of Oncology), University Hospital Vall d'Hebron, Barcelona, Spain; Facultat de Medicina, Universitat Autonoma de Barcelona, Bellaterra, Spain.

Classifications MeSH