Evaluation of Second-Line Chemotherapy with Docetaxel and Nedaplatin for Advanced or Recurrent Squamous Cell Carcinoma of the Esophagus
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- Miura Akinori
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Nagai Kagami
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Kojima Kazuyuki
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Yamada Hiroyuki
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Nishikage Tetsurou
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Inokuchi Mikito
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Nakajima Yasuaki
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Sekita Yoshihisa
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Ogiya Kazuo
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Tanaka Kouji
- Department of Surgery, Tokyo Medical and Dental University Hospital
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- Kawano Tatsuyuki
- Department of Surgery, Tokyo Medical and Dental University Hospital
Bibliographic Information
- Other Title
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- 進行・再発食道癌に対するsecond‐lineとしてのDocetaxel+Nedaplatin併用療法の検討
- 進行・再発食道癌に対するsecond-lineとしてのDocetaxel+Nedaplatin併用療法の検討
- シンコウ サイハツ ショクドウガン ニ タイスル second line ト シテ ノ Docetaxel Nedaplatin ヘイヨウ リョウホウ ノ ケントウ
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Abstract
We evaluated the efficacy and safety of a new combination chemotherapy including Docetaxel (TXT) and Nedaplatin (CDGP) as a second-line treatment for the advanced or recurrent esophageal carcinomas. Subsequent to administration of TXT at a dose of 60 mg for 60 minutes, CDGP was administered intravenously at a dose of 80 mg for 60 minutes. A total of nine male and one female with a median age of 65 (range 56-70) years were included and had been treated with prior chemotherapy. Prior treatments consisted of surgery and adjuvant chemoradiotherapy in 4 patients, surgery and adjuvant chemotherapy in 1 patient, chemotherapy for recurrent lesion after surgery in 3 patients, and chemotherapy alone in 2 patients. Eight patients underwent one course of treatment, 1 had two and 1 had three courses. Two PRs, 6 SDs and 2 NCs were obtained in all patients and the overall response rate was 20%. Median survival time was 170 days and median response time was 135 days. The prevailing toxicity was myelo-suppression with Grade 3 and 4 neutropenia occurring in 5 and 2 patients, respectively. The findings of this study indicated that a combination chemotherapy of TXT and CDGP is effective as a second-line treatment for advanced or recurrent esophageal cancers ; however, further investigations are needed to establish its efficacy.
Journal
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- Nihon Kikan Shokudoka Gakkai Kaiho
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Nihon Kikan Shokudoka Gakkai Kaiho 56 (4), 336-342, 2005
The Japan Broncho-esophagological Society
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Details 詳細情報について
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- CRID
- 1390282679989748224
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- NII Article ID
- 10016787026
- 130004469751
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- NII Book ID
- AN00187474
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- ISSN
- 18806848
- 00290645
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- NDL BIB ID
- 7446226
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed