Literature DB >> 12925072

Adjuvant therapy for rectal cancer--the transatlantic view.

B D Minsky1.   

Abstract

In North America there are two conventional treatments for clinically resectable rectal cancer. First is surgery and, if the tumour is T3 and/or N1-2, this is followed by postoperative combined modality therapy. The second, for patients with ultrasound T3 or clinical T4 disease, is pre-operative combined modality therapy followed by surgery and postoperative chemotherapy. Pre-operative therapy (most commonly combined modality therapy) has gained acceptance as a standard adjuvant therapy. The potential advantages of this approach compared with postoperative therapy include less acute toxicity and enhanced sphincter preservation. Recently completed randomized trials in the US and Germany will provide a definitive answer to this theory. In contrast to the combined modality approach to pre-operative therapy a number of European centres advocate an intensive short course of radiation (5 Gy x 5 followed one week later by surgery). The only randomized trial which has revealed a significant advantage in survival is the Swedish Rectal Cancer Trial. The Dutch CKVO 95-04 TME trial did not confirm a survival advantage and two metanalyses report conflicting results. Due to selection bias, it is not possible accurately to compare the local recurrence and survival results of intensive short course radiation with conventional pre-operative combined modality therapy. The intensive short course radiation approach is not used in North America due to its higher toxicity and lack of sphincter preservation. In the Dutch trial the 5-year local recurrence was 12% with TME and was significantly decreased to 6% with pre-operative radiation. The 5-year local recurrence rate in the 324 patients with stage III disease who underwent a TME alone with negative margins was 20%. Therefore, despite TME surgery, radiation therapy is still a necessary component in the adjuvant management of rectal cancer.

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Year:  2003        PMID: 12925072     DOI: 10.1046/j.1463-1318.2003.00504.x

Source DB:  PubMed          Journal:  Colorectal Dis        ISSN: 1462-8910            Impact factor:   3.788


  6 in total

Review 1.  Chemoradiotherapy and adjuvant chemotherapy for rectal cancer.

Authors:  Toshiaki Watanabe
Journal:  Int J Clin Oncol       Date:  2008-12-18       Impact factor: 3.402

2.  Effectiveness of gene expression profiling for response prediction of rectal adenocarcinomas to preoperative chemoradiotherapy.

Authors:  B Michael Ghadimi; Marian Grade; Michael J Difilippantonio; Sudhir Varma; Richard Simon; Cristina Montagna; Laszlo Füzesi; Claus Langer; Heinz Becker; Torsten Liersch; Thomas Ried
Journal:  J Clin Oncol       Date:  2005-03-20       Impact factor: 44.544

3.  [PET/CT for colorectal and hepatic tumors].

Authors:  J Stollfuss; H Wieder; E Rummeny; M Schwaiger
Journal:  Radiologe       Date:  2004-11       Impact factor: 0.635

4.  Circadian gene expression predicts patient response to neoadjuvant chemoradiation therapy for rectal cancer.

Authors:  Haijie Lu; Qiqi Chu; Guojiang Xie; Hao Han; Zheng Chen; Benhua Xu; Zhicao Yue
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

5.  Local excision for ypT2 rectal cancer--much ado about something.

Authors:  Rodrigo O Perez; Angelita Habr-Gama; Igor Proscurshim; Fábio G Campos; Desiderio Kiss; Joaquim Gama-Rodrigues; Ivan Cecconello
Journal:  J Gastrointest Surg       Date:  2007-09-06       Impact factor: 3.452

6.  The clinicopathological features of colorectal mucinous adenocarcinoma and a therapeutic strategy for the disease.

Authors:  Masakatsu Numata; Manabu Shiozawa; Takuo Watanabe; Hiroshi Tamagawa; Naoto Yamamoto; Soichiro Morinaga; Kazuteru Watanabe; Teni Godai; Takashi Oshima; Shoichi Fujii; Chikara Kunisaki; Yasushi Rino; Munetaka Masuda; Makoto Akaike
Journal:  World J Surg Oncol       Date:  2012-06-15       Impact factor: 2.754

  6 in total

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