Literature DB >> 19822509

Improved patient and regimen selection in locally advanced rectal cancer: who, how, and what next?

Jared Weiss1, Drew Moghanaki, John P Plastaras, Daniel G Haller.   

Abstract

Before the advent of neoadjuvant chemoradiation therapy (NCRT) for locally advanced rectal cancer, local failure represented half of treatment failures. The German Rectal Cancer Study Group trial demonstrated that NCRT along with total mesorectal excision can improve local control and the rate of sphincter-preserving surgery. Thus, the National Comprehensive Cancer Network now recommends NCRT as the standard of care for stage III and IV rectal cancer. Recent trials and analysis have questioned accepted wisdom regarding patient selection for NCRT and methods of administration. EORTC 22921 demonstrated that the addition of chemotherapy to radiation therapy, regardless of timing, improved local control but not overall survival, and subgroup analysis from this study generated the hypothesis that the subgroup of patients with good pathologic response to NCRT would benefit the most from additional chemotherapy following surgery. The prognosis of rectal cancer is stage dependent, and 2 major analyses question whether T1/2 N1 and T3 N0 patients benefit from NCRT. Application of the results from these studies is hindered by imperfections in staging. Future improvement in patient selection might result from biologic analysis of tumor sensitivity. NCRT might be improved with the use of oral fluoropyrimidines and perhaps the addition of a second agent such as oxaliplatin, irinotecan, or cetuximab. Improvements in radiation, such as the use of more conformal techniques, might decrease the toxicity of therapy. Given the success of NCRT in improving local control, distant metastasis now predominates as the cause of treatment failure, and larger gains will likely be made from improvements in adjuvant chemotherapy.

Entities:  

Mesh:

Year:  2009        PMID: 19822509     DOI: 10.3816/CCC.2009.n.033

Source DB:  PubMed          Journal:  Clin Colorectal Cancer        ISSN: 1533-0028            Impact factor:   4.481


  4 in total

1.  Antitumor activity of mutant bacterial cytosine deaminase gene for colon cancer.

Authors:  Long-Ying Deng; Jian-Ping Wang; Zhi-Fu Gui; Li-Zong Shen
Journal:  World J Gastroenterol       Date:  2011-06-28       Impact factor: 5.742

2.  Pre- and post-surgery treatments in rectal cancer: a long-term single-centre experience.

Authors:  H Ozyurt; A S Ozden; Z Ozgen; C Gemici; G Yaprak
Journal:  Curr Oncol       Date:  2017-02-27       Impact factor: 3.677

3.  Adjuvant chemoradiotherapy of advanced resectable rectal cancer: results of a randomised trial comparing modulation of 5-fluorouracil with folinic acid or with interferon-α.

Authors:  M Kornmann; L Staib; T Wiegel; E-D Kreuser; M Kron; W Baumann; D Henne-Bruns; K-H Link
Journal:  Br J Cancer       Date:  2010-09-28       Impact factor: 7.640

4.  Genomic alterations in rectal tumors and response to neoadjuvant chemoradiotherapy: an exploratory study.

Authors:  Chiara Molinari; Michela Ballardini; Nazario Teodorani; Massimo Giannini; Wainer Zoli; Ermanno Emiliani; Enrico Lucci; Alessandro Passardi; Paola Rosetti; Luca Saragoni; Massimo Guidoboni; Dino Amadori; Daniele Calistri
Journal:  Radiat Oncol       Date:  2011-11-18       Impact factor: 3.481

  4 in total

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