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  1. 原著論文

Phase II trial of oral S-1 combined with gemcitabine in metastatic pancreatic cancer

https://repo.qst.go.jp/records/44880
https://repo.qst.go.jp/records/44880
f612b552-35e4-4d46-85ee-83d1d236c0e3
Item type 学術雑誌論文 / Journal Article(1)
公開日 2007-06-15
タイトル
タイトル Phase II trial of oral S-1 combined with gemcitabine in metastatic pancreatic cancer
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Nakamura, Kazutaka

× Nakamura, Kazutaka

WEKO 445745

Nakamura, Kazutaka

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Yamaguti, Taketo

× Yamaguti, Taketo

WEKO 445746

Yamaguti, Taketo

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Ishihara, Takeshi

× Ishihara, Takeshi

WEKO 445747

Ishihara, Takeshi

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Kobayashi, Akitoshi

× Kobayashi, Akitoshi

WEKO 445748

Kobayashi, Akitoshi

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Tadenuma, Hiroshi

× Tadenuma, Hiroshi

WEKO 445749

Tadenuma, Hiroshi

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Sudo, Kentaro

× Sudo, Kentaro

WEKO 445750

Sudo, Kentaro

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Katou, Hirotoshi

× Katou, Hirotoshi

WEKO 445751

Katou, Hirotoshi

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Saisho, Hiromitsu

× Saisho, Hiromitsu

WEKO 445752

Saisho, Hiromitsu

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山口 武人

× 山口 武人

WEKO 445753

en 山口 武人

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加藤 博敏

× 加藤 博敏

WEKO 445754

en 加藤 博敏

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税所 宏光

× 税所 宏光

WEKO 445755

en 税所 宏光

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抄録
内容記述タイプ Abstract
内容記述 We conducted a phase II trial of gemcitabine with S-1, oral fluorouracil (5-FU) prodrug tegafur combined with two modulators, 5-chloro-2, 4-dihydroxypyridine and potassium oxonate, to evaluate the activity and toxicity of such a combination in metastatic pancreatic cancer (MPC) patients. Patients who had pathologically proven pancreatic cancer with metastatic lesions were eligible candidates for entry into the study. S-1 was given orally (30 mg m(-2)) b.i.d. for 14 consecutive days and gemcitabine (1000 mg m(-2)) was given on days 8 and 15. The cycle was repeated every 21 days. We enrolled 33 MPC patients. The median number of cycles was eight (range 1-20). Grade 3-4 toxicities were leucopenia (33%), neutropenia (55%), anaemia (9%), thrombocytopenia (15%), anorexia (6%), fever (9%), and interstitial pneumonia (6%). Objective responses were obtained in 16 patients (one complete response and 15 partial responses; response rate, 48%; 95% confidence interval (CI), 33-65). Median survival and 1-year survival rate were 12.5 months (95% CI, 5.9-19.1) and 54% (95% CI, 36-72), respectively. Combination chemotherapy with GEM and S-1 was well tolerated and yielded a significantly high response rate.
書誌情報 British Journal of Cancer

巻 94, 号 11, p. 1575-1579, 発行日 2006-06
ISSN
収録物識別子タイプ ISSN
収録物識別子 0007-0920
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