New developments in the treatment of esophageal cancer Journal Article


Author: Ilson, D. H.
Article Title: New developments in the treatment of esophageal cancer
Abstract: Esophageal cancer is a rare but highly virulent malignancy in the United States and Western Europe, and adenocarcinoma of the esophagus has had the most rapid rate of increase of any solid tumor malignancy. Combined chemoradiotherapy is the standard of care in the nonsurgical management of esophageal cancer. Trials of preoperative chemotherapy followed by surgery have not shown a consistent benefit. Preoperative chemoradiotherapy followed by surgery continues to be actively studied in the surgical management of locally advanced esophageal cancer. Pathologic complete responses are seen in 20% to 40% of patients, with 5-year survival achieved in 30% to 35%. Newer agents, such as the taxanes and irinotecan, have been evaluated in combined chemoradiotherapy trials. These trials have shown promising antitumor activity and therapy tolerance, depending on the dose and schedule of therapy administered. Increasing the dose of radiotherapy, or adding a brachytherapy boost to chemoradiotherapy, has not improved the outcome of treatment in clinical trials. The advent of newer targeted therapies, including agents directed against growth factor receptor pathways, tumor angiogenesis, and tumor invasion and metastasis, is leading to a new generation of clinical trials combining these agents with conventional cytotoxic chemotherapy and radiation.
Keywords: survival rate; mortality; review; multimodality cancer therapy; paclitaxel; combined modality therapy; antineoplastic agent; antineoplastic combined chemotherapy protocols; antineoplastic agents, phytogenic; camptothecin; irinotecan; drug derivative; esophagus tumor; esophageal neoplasms; humans; human
Journal Title: Current Oncology Reports
Volume: 4
Issue: 3
ISSN: 1523-3790
Publisher: Springer  
Date Published: 2002-06-01
Start Page: 213
End Page: 221
Language: English
PUBMED: 11937011
PROVIDER: scopus
DOI: 10.1007/s11912-002-0018-y
DOI/URL:
Notes: Export Date: 14 November 2014 -- Source: Scopus
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  1. David H Ilson
    433 Ilson
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