Literature DB >> 24278852

Additional chemotherapy during resting periods after preoperative chemoradiotherapy in patients with rectal cancer.

Ok Suk Bae1.   

Abstract

Entities:  

Year:  2013        PMID: 24278852      PMCID: PMC3837079          DOI: 10.3393/ac.2013.29.5.178

Source DB:  PubMed          Journal:  Ann Coloproctol        ISSN: 2287-9714


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See Article on Page 192-197 The advantages of preoperative chemoradiotherpy are tumor downstaging and to minimize seeding of tumor cells during surgery, but it has two problems awaiting solution. The first problem is low rate of complete response. Rectal cancer is known to be radioresistant compared with anal cancer. If a higher response rate is to be obtained, a concomitant chemotherapy method is needed because chemotherapy sensitizes tumor cells to radiation. The second problem is the long treatment time, including the resting time after completion of chemoradiation, because surgery is performed approximately after 6 weeks following the completion of chemoradiotherapy. Because cancer will not be treated during the resting time, some are apprehensive about the dangers of cancer being aggravated and metastatic lesions from remnant cancer occurring during the resting time. I support the conclusion that additional chemotherapy is one of the methods to resolve these problems in spite of these demerits. If additional chemotherapy can downstage a tumor more than conventional chemoradiation, it will be a very useful treatment method for rectal cancer patients. In this article, authors report that they tried an additional four weeks of chemotherapy with capecitabine during resting periods. They did not obtain a visibly better result; nonetheless, this article bears prospective meanings [1]. Fontana [2] reported encouraging results for preoperative 5-FU-oxaliplatin chemoradiation therapy in locally advanced rectal cancer. In the near future, new drugs and molecular studies will be developed, and these may lead to much better results [3]. Therefore, additional study will be needed to realize improvements in preoperative control for rectal cancer. I envisage that future patients with rectal cancer will get much benefit from additional chemotherapy and that a small number of them will be cured without surgery.
  3 in total

1.  miRNA expressions in rectal cancer as predictors of response to neoadjuvant chemoradiation therapy.

Authors:  Elrasheid A H Kheirelseid; Nicola Miller; Kah Hoong Chang; Catherine Curran; Emer Hennessey; Margaret Sheehan; John Newell; Christophe Lemetre; Graham Balls; Michael J Kerin
Journal:  Int J Colorectal Dis       Date:  2012-08-18       Impact factor: 2.571

2.  Long-term results of preoperative 5-fluorouracil-oxaliplatin chemoradiation therapy in locally advanced rectal cancer.

Authors:  Elisa Fontana; Francesca Pucci; Roberta Camisa; Simona Bui; Salvatore Galdy; Francesco Leonardi; Francesca Virginia Negri; Elisa Anselmi; Pier Luigi Losardo; Luigi Roncoroni; Paolo Dell'abate; Pellegrino Crafa; Stefano Cascinu; Andrea Ardizzoni
Journal:  Anticancer Res       Date:  2013-02       Impact factor: 2.480

3.  A Phase II Study of Additional Four-Week Chemotherapy With Capecitabine During the Resting Periods After Six-Week Neoadjuvant Chemoradiotherapy in Patients With Locally Advanced Rectal Cancer.

Authors:  Kyung Ha Lee; Min Sang Song; Jun Boem Park; Jin Soo Kim; Dae Young Kang; Ji Yeon Kim
Journal:  Ann Coloproctol       Date:  2013-10-31
  3 in total

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