Literature DB >> 15031598

Response to chemotherapy (irinotecan plus 5-fluorouracil) in colorectal carcinoma can be predicted by tumour DNA content.

R Bendardaf1, H Lamlum, R Ristamäki, A Algars, Y Collan, S Pyrhönen.   

Abstract

OBJECTIVE: The aim of this study was to identify markers that might predict response to chemotherapy. Postoperative chemotherapy improves the outcome in stage III colon cancer and is widely accepted as a standard therapy, but there are currently no reliable predictors to identify and select patients that will benefit.
METHODS: Using DNA image cytometry, the DNA content was determined from the isolated nuclei of 56 primary colorectal carcinomas of patients who received chemotherapy (either irinotecan or irinotecan plus 5-fluorouracil and folinic acid) for advanced disease. Response to chemotherapy could be reliably evaluated in 53 patients.
RESULTS: The modal DNA content (ploidy status) of the tumour correlated with the observed response to chemotherapy (p = 0.01). An objective response was observed in 56% of patients whose tumour histograms displayed tetraploid, peri-tetraploid or multiploid patterns of peaks, compared with 19% in patients with diploid, peri-diploid or aneuploid peaks. Notably, 86% (6/7) of patients whose tumours displayed a multiploid peak pattern showed an objective response and 1 patient had stable disease.
CONCLUSIONS: This study suggests that modal DNA content can be used to predict a patient's response to chemotherapy in advanced colorectal carcinoma. This may help in identifying patients who will benefit most from therapy for advanced colorectal cancer. Copyright 2004 S. Karger AG, Basel

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Year:  2004        PMID: 15031598     DOI: 10.1159/000076334

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  5 in total

1.  Aneuploidy and elevated CEA indicate an increased risk for metachronous metastasis in colorectal cancer.

Authors:  Tilman Laubert; Verena Bente; Sandra Freitag-Wolf; Helena Voulgaris; Martina Oberländer; Katharina Schillo; Markus Kleemann; Conny Bürk; Hans-Peter Bruch; Uwe J Roblick; Jens K Habermann
Journal:  Int J Colorectal Dis       Date:  2013-01-08       Impact factor: 2.571

Review 2.  Stage-specific frequency and prognostic significance of aneuploidy in patients with sporadic colorectal cancer--a meta-analysis and current overview.

Authors:  Tilman Laubert; Sandra Freitag-Wolf; Michael Linnebacher; Alexandra König; Brigitte Vollmar; Jens K Habermann
Journal:  Int J Colorectal Dis       Date:  2015-06-09       Impact factor: 2.571

3.  Evaluation of novel histone deacetylase inhibitors as therapeutic agents for colorectal adenocarcinomas compared to established regimens with the histoculture drug response assay.

Authors:  Jin C Kim; Dae D Kim; Yoo M Lee; Tae W Kim; Dong H Cho; Moon B Kim; Seong G Ro; Seon Y Kim; Yong S Kim; Jung S Lee
Journal:  Int J Colorectal Dis       Date:  2008-10-01       Impact factor: 2.571

4.  Loss of MUC2 expression predicts disease recurrence and poor outcome in colorectal carcinoma.

Authors:  Adam Elzagheid; Fatma Emaetig; Abdelbaset Buhmeida; Matti Laato; Omran El-Faitori; Kari Syrjänen; Yrjö Collan; Seppo Pyrhönen
Journal:  Tumour Biol       Date:  2012-11-21

5.  The Phenoxyphenol Compound 4-HPPP Selectively Induces Antiproliferation Effects and Apoptosis in Human Lung Cancer Cells through Aneupolyploidization and ATR DNA Repair Signaling.

Authors:  Wangta Liu; Chang-Yi Wu; Mei-Jei Lu; Yung-Jen Chuang; Eing-Mei Tsai; Steve Leu; I-Ling Lin; Chih-Jan Ko; Chien-Chih Chiu; Wen-Tsan Chang
Journal:  Oxid Med Cell Longev       Date:  2020-01-07       Impact factor: 6.543

  5 in total

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