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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3827058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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