Abstract | PURPOSE: METHODS: Fourteen patients with esophageal cancer enrolled in this dose escalation study to determine the RD for a phase III trial. Efficacy and toxicity in DCF-RT of RD were evaluated in 37 patients with esophageal cancer. RESULTS: The RD for DCF-RT for esophageal cancer in the present study was 50 mg/m(2) docetaxel plus 60 mg/m(2) cisplatin on day 1 and day 29 plus 600 mg/m(2) 5-FU on days 1-4 and days 29-32 and concurrent radiation of 60 Gy/30 fractions/6 weeks. The main toxicities were myelotoxicity and radiation esophagitis. In this phase I/II study, we could have safety and feasibility by RD, because there was low mortality and most toxicities were manageable level. The complete response (CR) rate and response rate were 54.1 and 83.8 %, respectively, in the phase II study. In patients with a classification of clinical T4, the CR rate and response rate were 47.6 and 85.7 %, respectively. The 2-year overall survival rate, 2-year progression-free survival rate, and median survival time (MST) were 52.9, 50.0 %, and 24.7 months, respectively. In patients with clinical T4 classification, the 2-year overall survival rate, 2-year progression-free survival rate, and MST were 43.5, 44.9 %, and 21.6 months respectively. CONCLUSIONS: DCF-RT keeps safety and feasibility by management of myelotoxicity adequately in RD. This protocol might produce a high CR rate and favorable prognosis compared with standard chemoradiotherapy for advanced esophageal cancer.
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Authors | Tatsuya Miyazaki, Makoto Sohda, Naritaka Tanaka, Shigemasa Suzuki, Keisuke Ieta, Makoto Sakai, Akihiko Sano, Takehiko Yokobori, Takanori Inose, Masanobu Nakajima, Minoru Fukuchi, Hitoshi Ojima, Hiroyuki Kato, Hiroyuki Kuwano |
Journal | Cancer chemotherapy and pharmacology
(Cancer Chemother Pharmacol)
Vol. 75
Issue 3
Pg. 449-55
(Mar 2015)
ISSN: 1432-0843 [Electronic] Germany |
PMID | 25544126
(Publication Type: Clinical Trial, Phase I, Clinical Trial, Phase II, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Taxoids
- Docetaxel
- Cisplatin
- Fluorouracil
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Topics |
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage, adverse effects, therapeutic use)
- Chemoradiotherapy
(adverse effects, methods)
- Cisplatin
(administration & dosage)
- Disease-Free Survival
- Docetaxel
- Dose-Response Relationship, Drug
- Esophageal Neoplasms
(pathology, therapy)
- Feasibility Studies
- Female
- Fluorouracil
(administration & dosage)
- Humans
- Male
- Middle Aged
- Prospective Studies
- Survival Rate
- Taxoids
(administration & dosage)
- Treatment Outcome
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