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[接受顺铂与S-1或顺铂与盐酸伊立替康一线联合化疗的晚期或复发性胃癌患者严重血液学毒性相关风险]

[Risk associated with severe hematological toxicity in patients with advanced or recurrent gastric cancer receiving primary combination chemotherapy of cisplatin and S-1 or cisplatin and irinotecan hydrochloride].

作者信息

Sunaga Tomiko, Suzuki Shuji, Harada Nobuhiko, Tanaka Seiichi, Hayashi Tsuneo, Suzuki Mamoru

机构信息

Department of Pharmacy, Hachioji Digestive Hospital.

出版信息

Gan To Kagaku Ryoho. 2009 Apr;36(4):589-93.

Abstract

The purpose of this study was to analyze the risk factor for grade 3 to 4 hematological toxicity after primary chemotherapy(cisplatin(CDDP)/tegafur, gimeracil, oteracil potassium(S1)or CDDP/irinotecan hydrochloride(CPT-11)) in 75 patients with unresectable or recurrent gastric cancer between April 2005 and May 2008. The rate of grade 3 to 4 hematological toxicity was 17.3%(13 patients). Grade 3 to 4 hematological toxicity was the endpoint selected for the analysis. At multivariate analysis, the most important pretreatment risk factors for grade 3 to 4 hematological toxicity in patients receiving primary chemotherapy of unresectable or recurrent gastric cancer were found to be hemoglobin(OR 0.520; p=0.012)and treatment regimen(CDDP/CPT-11)(OR 0.101; p=0.002). Therefore, patients about to receive chemotherapy should be considered in these risk factors.

摘要

本研究旨在分析2005年4月至2008年5月期间75例不可切除或复发性胃癌患者接受一线化疗(顺铂(CDDP)/替吉奥(S-1)或CDDP/盐酸伊立替康(CPT-11))后发生3-4级血液学毒性的危险因素。3-4级血液学毒性发生率为17.3%(13例患者)。3-4级血液学毒性为选定的分析终点。多因素分析发现,不可切除或复发性胃癌患者接受一线化疗时,发生3-4级血液学毒性的最重要预处理危险因素为血红蛋白(OR 0.520;p=0.012)和治疗方案(CDDP/CPT-11)(OR 0.101;p=0.002)。因此,在考虑这些危险因素时应关注即将接受化疗的患者。

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