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Microsatellite instability & survival in patients with stage II/III colorectal carcinoma
BACKGROUND & OBJECTIVES: The two key aspects associated with the microsatellite instability (MSI) as genetic phenomenon in colorectal cancer (CRC) are better survival prognosis, and the varying response to 5-fluorouracil (5-FU)-based chemotherapy. This study was undertaken to measure the surviva...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080918/ https://www.ncbi.nlm.nih.gov/pubmed/27748284 http://dx.doi.org/10.4103/0971-5916.191801 |
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author | Srdjan, Markovic Jadranka, Antic Ivan, Dimitrijevic Branimir, Zogovic Daniela, Bojic Petar, Svorcan Velimir, Markovic Zoran, Krivokapic |
author_facet | Srdjan, Markovic Jadranka, Antic Ivan, Dimitrijevic Branimir, Zogovic Daniela, Bojic Petar, Svorcan Velimir, Markovic Zoran, Krivokapic |
author_sort | Srdjan, Markovic |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: The two key aspects associated with the microsatellite instability (MSI) as genetic phenomenon in colorectal cancer (CRC) are better survival prognosis, and the varying response to 5-fluorouracil (5-FU)-based chemotherapy. This study was undertaken to measure the survival of surgically treated patients with stages II and III CRC based on the MSI status, the postoperative 5-FU treatment as well as clinical and histological data. METHODS: A total of 125 consecutive patients with stages II and III (American Joint Committee on Cancer, AJCC staging) primary CRCs, were followed prospectively for a median time of 31 months (January 2006 to December 2009). All patients were assessed, operated and clinically followed. Tumour samples were obtained for cytopathological verification and MSI grading. RESULTS: Of the 125 patients, 21 (20%) had high MSI (MSI-H), and 101 patients (80%) had MSI-L or MSS (low frequency MSI or stable MSI). Patients with MSS CRC were more likely to have recurrent disease (P=0.03; OR=3.2; CI 95% 1-10.2) compared to those with MSI-H CRC. Multi- and univariate Cox regression analysis failed to show a difference between MSI-H and MSS groups with respect to disease-free, disease-specific and overall survival. However, the disease-free survival was significantly lower in patients with MSI-H CRC treated by adjuvant 5-FU therapy (P=0.03). INTERPRETATION & CONCLUSIONS: MSI-H CRCs had a lower recurrence rate, but the prognosis was worse following adjuvant 5-FU therapy. |
format | Online Article Text |
id | pubmed-5080918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50809182016-11-14 Microsatellite instability & survival in patients with stage II/III colorectal carcinoma Srdjan, Markovic Jadranka, Antic Ivan, Dimitrijevic Branimir, Zogovic Daniela, Bojic Petar, Svorcan Velimir, Markovic Zoran, Krivokapic Indian J Med Res Original Article BACKGROUND & OBJECTIVES: The two key aspects associated with the microsatellite instability (MSI) as genetic phenomenon in colorectal cancer (CRC) are better survival prognosis, and the varying response to 5-fluorouracil (5-FU)-based chemotherapy. This study was undertaken to measure the survival of surgically treated patients with stages II and III CRC based on the MSI status, the postoperative 5-FU treatment as well as clinical and histological data. METHODS: A total of 125 consecutive patients with stages II and III (American Joint Committee on Cancer, AJCC staging) primary CRCs, were followed prospectively for a median time of 31 months (January 2006 to December 2009). All patients were assessed, operated and clinically followed. Tumour samples were obtained for cytopathological verification and MSI grading. RESULTS: Of the 125 patients, 21 (20%) had high MSI (MSI-H), and 101 patients (80%) had MSI-L or MSS (low frequency MSI or stable MSI). Patients with MSS CRC were more likely to have recurrent disease (P=0.03; OR=3.2; CI 95% 1-10.2) compared to those with MSI-H CRC. Multi- and univariate Cox regression analysis failed to show a difference between MSI-H and MSS groups with respect to disease-free, disease-specific and overall survival. However, the disease-free survival was significantly lower in patients with MSI-H CRC treated by adjuvant 5-FU therapy (P=0.03). INTERPRETATION & CONCLUSIONS: MSI-H CRCs had a lower recurrence rate, but the prognosis was worse following adjuvant 5-FU therapy. Medknow Publications & Media Pvt Ltd 2016-05 /pmc/articles/PMC5080918/ /pubmed/27748284 http://dx.doi.org/10.4103/0971-5916.191801 Text en Copyright: © Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Srdjan, Markovic Jadranka, Antic Ivan, Dimitrijevic Branimir, Zogovic Daniela, Bojic Petar, Svorcan Velimir, Markovic Zoran, Krivokapic Microsatellite instability & survival in patients with stage II/III colorectal carcinoma |
title | Microsatellite instability & survival in patients with stage II/III colorectal carcinoma |
title_full | Microsatellite instability & survival in patients with stage II/III colorectal carcinoma |
title_fullStr | Microsatellite instability & survival in patients with stage II/III colorectal carcinoma |
title_full_unstemmed | Microsatellite instability & survival in patients with stage II/III colorectal carcinoma |
title_short | Microsatellite instability & survival in patients with stage II/III colorectal carcinoma |
title_sort | microsatellite instability & survival in patients with stage ii/iii colorectal carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080918/ https://www.ncbi.nlm.nih.gov/pubmed/27748284 http://dx.doi.org/10.4103/0971-5916.191801 |
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