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Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach

BACKGROUND: Recently, a new classification for gastric cancer (GC) has been proposed, based on Lauren's histology and on anatomic tumour location, identifying three subtypes of disease: type 1 (proximal non diffuse GC), type 2 (diffuse GC) and type 3 (distal non diffuse GC). Aim of our analysis...

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Autores principales: Bittoni, Alessandro, Scartozzi, Mario, Giampieri, Riccardo, Faloppi, Luca, Bianconi, Maristella, Mandolesi, Alessandra, Prete, Michela Del, Pistelli, Mirco, Cecchini, Luca, Bearzi, Italo, Cascinu, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827058/
https://www.ncbi.nlm.nih.gov/pubmed/24265697
http://dx.doi.org/10.1371/journal.pone.0078544
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author Bittoni, Alessandro
Scartozzi, Mario
Giampieri, Riccardo
Faloppi, Luca
Bianconi, Maristella
Mandolesi, Alessandra
Prete, Michela Del
Pistelli, Mirco
Cecchini, Luca
Bearzi, Italo
Cascinu, Stefano
author_facet Bittoni, Alessandro
Scartozzi, Mario
Giampieri, Riccardo
Faloppi, Luca
Bianconi, Maristella
Mandolesi, Alessandra
Prete, Michela Del
Pistelli, Mirco
Cecchini, Luca
Bearzi, Italo
Cascinu, Stefano
author_sort Bittoni, Alessandro
collection PubMed
description BACKGROUND: Recently, a new classification for gastric cancer (GC) has been proposed, based on Lauren's histology and on anatomic tumour location, identifying three subtypes of disease: type 1 (proximal non diffuse GC), type 2 (diffuse GC) and type 3 (distal non diffuse GC). Aim of our analysis was to compare clinical outcome according to different GC subtypes (1,2,3) in metastatic GC patients receiving first-line chemotherapy. PATIENTS AND METHODS: Advanced GC pts treated with a first-line combination chemotherapy were included in our analysis. Pts were divided in three subgroups (type 1, type 2 and type 3) as previously defined. RESULTS: A total of 248 advanced GC pts were included: 45.2% belonged to type 2, 43.6% to type 3 and 11.2% to type 1. Patients received a fluoropyrimidine-based chemotherapy doublet or three drugs regimens including a platinum derivate and a fluoropyrimidine with the addition of an anthracycline, a taxane or mytomicin C. RR was higher in type 1 pts (RR = 46.1%) and type 3 (34,3%) compared to type 2 (20,4%), (p = 0.015). Type 2 presented a shorter PFS, median PFS = 4.2 months, compared to type 1, mPFS = 7.2 months, and type 3, mPFS = 5.9 months (p = 0.011) and also a shorter OS (p = 0.022). CONCLUSIONS: Our analysis suggests that GC subtypes may be important predictors of benefit from chemotherapy in advanced GC patients. Future clinical trials should take in account these differences for a better stratification of patients.
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spelling pubmed-38270582013-11-21 Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach Bittoni, Alessandro Scartozzi, Mario Giampieri, Riccardo Faloppi, Luca Bianconi, Maristella Mandolesi, Alessandra Prete, Michela Del Pistelli, Mirco Cecchini, Luca Bearzi, Italo Cascinu, Stefano PLoS One Research Article BACKGROUND: Recently, a new classification for gastric cancer (GC) has been proposed, based on Lauren's histology and on anatomic tumour location, identifying three subtypes of disease: type 1 (proximal non diffuse GC), type 2 (diffuse GC) and type 3 (distal non diffuse GC). Aim of our analysis was to compare clinical outcome according to different GC subtypes (1,2,3) in metastatic GC patients receiving first-line chemotherapy. PATIENTS AND METHODS: Advanced GC pts treated with a first-line combination chemotherapy were included in our analysis. Pts were divided in three subgroups (type 1, type 2 and type 3) as previously defined. RESULTS: A total of 248 advanced GC pts were included: 45.2% belonged to type 2, 43.6% to type 3 and 11.2% to type 1. Patients received a fluoropyrimidine-based chemotherapy doublet or three drugs regimens including a platinum derivate and a fluoropyrimidine with the addition of an anthracycline, a taxane or mytomicin C. RR was higher in type 1 pts (RR = 46.1%) and type 3 (34,3%) compared to type 2 (20,4%), (p = 0.015). Type 2 presented a shorter PFS, median PFS = 4.2 months, compared to type 1, mPFS = 7.2 months, and type 3, mPFS = 5.9 months (p = 0.011) and also a shorter OS (p = 0.022). CONCLUSIONS: Our analysis suggests that GC subtypes may be important predictors of benefit from chemotherapy in advanced GC patients. Future clinical trials should take in account these differences for a better stratification of patients. Public Library of Science 2013-11-12 /pmc/articles/PMC3827058/ /pubmed/24265697 http://dx.doi.org/10.1371/journal.pone.0078544 Text en © 2013 Bittoni et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bittoni, Alessandro
Scartozzi, Mario
Giampieri, Riccardo
Faloppi, Luca
Bianconi, Maristella
Mandolesi, Alessandra
Prete, Michela Del
Pistelli, Mirco
Cecchini, Luca
Bearzi, Italo
Cascinu, Stefano
Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach
title Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach
title_full Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach
title_fullStr Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach
title_full_unstemmed Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach
title_short Clinical Evidence for Three Distinct Gastric Cancer Subtypes: Time for a New Approach
title_sort clinical evidence for three distinct gastric cancer subtypes: time for a new approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827058/
https://www.ncbi.nlm.nih.gov/pubmed/24265697
http://dx.doi.org/10.1371/journal.pone.0078544
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