Preoperative chemoradiotherapy for rectal cancer: Experience from one centre

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TitrePreoperative chemoradiotherapy for rectal cancer: Experience from one centre
Type de publicationJournal Article
Year of Publication2015
AuteursLescut N., Lepinoy A., Schipman B., Cerda T., Guimas V., Bednarek C., Bosset J.-F
JournalCANCER RADIOTHERAPIE
Volume19
Pagination98-105
Date PublishedAPR
Type of ArticleArticle
ISSN1278-3218
Mots-clésAdenocarcinoma of the rectum, Neoadjuvant chemoradiation
Résumé

Purpose. - In recent decades, the management of rectal cancer has been significantly improved by optimizing the surgical treatment with the total mesorectal excision and the development of neoadjuvant radiotherapy with or without chemotherapy. In this study, we investigated the impact of changes in practice over a period of 15 years in an expert centre. Patients and methods. - A monocentric study was conducted retrospectively on cT3-resectable T4 patients who received chemoradiotherapy for a locally advanced rectal adenocarcinoma between 1993 and 2008. We studied sphincter preservation, pathological complete response (ypT0), survival, and toxicities by different concomitant chemotherapy and treatment period. Results. - Among the 179 patients who had a chemoradiotherapy, 56.4% were received concomitant 5-fluoro-uracil-leucovorin, 28.5% with concomitant capecitabine, and 15.1% with concomitant oxaliplatin and capecitabine. The average dose of radiotherapy was 45 Gy (25 x 1.8 Gy). Five-year disease-free survival was 74.3% and overall survival 68.8%. The rate of local recurrence and distant metastases were 6.1 and 23.6%. In multivariate analysis, concomitant chemotherapy oxaliplatin and capecitabine improved the pathological complete response rate (ypT0; capecitabine: 6%, 5-fluoro-uracil-leucovorin: 10.3%, capecitabine-oxaliplatin: 22.2%), but not significantly (P = 0.12) and with more toxicities, and treatment interruptions. Sphincter preservation rate was not improved significantly during the study period (1993-2004 vs. 2005-2008), but disease-free survival improved from 72.2% up to 87.5% (P = 0.03). Conclusion. - Our results are consistent with those published in the literature. Concomitant chemotherapy with 5-fluoro-uracil or capecitabine remains the standard scheme. Upfront chemotherapy, before chemoradiotherapy, should be investigated with regard to the predominance of metastasis. (C) 2015 Published by Elsevier Masson SAS on behalf of the Societe francaise de radiotherapie oncologique (SFRO).

DOI10.1016/j.canrad.2014.11.011