This Article Full Text Full Text (PDF) eLetters: Submit a response to this article Purchase Article View Shopping Cart Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services E-mail this article link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints/Permissions Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Scagliotti, G. V. Articles by Turrisi, A. T. Search for Related Content PubMed PubMed Citation Articles by Scagliotti, G. V. Articles by Turrisi, A. T., III

Docetaxel-Based Combined-Modality Chemoradiotherapy for Locally Advanced Non-Small Cell Lung Cancer

^a University of Turin, Department of Clinical and Biological Sciences, S. Luigi Hospital, Thoracic Oncology Unit, Torino, Italy; ^b Medical University of South Carolina, Charleston, South Carolina, USA

Correspondence: Andrew T. Turrisi, III, M.D., Medical University of South Carolina, 169 Ashley Avenue, P.O. Box 250318, Charleston, South Carolina 29425, USA. Telephone: 843-792-3271; Fax: 843-792-5498; e-mail: turrisi{at}radonc.musc.edu

The cytotoxic agent docetaxel not only has proven activity in non-small cell lung cancer—when used alone or in combination—but is also a potent radiosensitizer, and improved treatments are needed in all stages of this disease. In patients with locoregionally advanced (stage III) disease, docetaxel has shown efficacy with manageable toxicities when used alone or in combination with a platinum compound in a sequential manner before localized radical radiotherapy/surgery. Presently, therapeutic gains appear to be maximized by the use of concurrent chemotherapy and irradiation. This review focuses on research with combinations of docetaxel with either cisplatin or carboplatin and radiotherapy. Overall response and survival rates to date provide data worth pursuing. From phase I data, weekly docetaxel at 20 mg/m² plus cisplatin at 25 mg/m² or carboplatin to an area under the concentration time curve of 2 mg/ml•min with concurrent radiotherapy to 60 Gy over 6 weeks appear to be suitable for phase II trials. Predominant toxicities are esophagitis and neutropenia, but a low frequency of pulmonary toxicity is reported. Induction, concurrent, and consolidation docetaxel-based chemoradiotherapy in potentially resectable disease are all being investigated. Future research could include the investigation of computed tomography/ positron emission tomography-derived target volume radiotherapy, dose-escalated therapy, and alternative fractionation schedules in combination with docetaxel-based cytotoxic chemotherapy.

Key Words. Chemotherapy • Docetaxel • Non-small cell lung carcinoma • Radiotherapy • Review