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FOLFOX方案(亚叶酸钙、氟尿嘧啶与奥沙利铂联合)作为转移性结直肠癌一线治疗的疗效与毒性

The efficacy and toxicity of FOLFOX regimen (a combination of leucovorin and fluorouracil with oxaliplatin) as first-line treatment of metastatic colorectal cancer.

作者信息

Matsushita Hidenobu, Tsuboi Kenji, Honda Ichiro, Kato Nobuyuki, Okochi Osamu, Kobayashi Daisuke, Hattori Masashi

机构信息

Dept. of Surgery, Tosei General Hospital, Aichi, Japan.

出版信息

Gan To Kagaku Ryoho. 2009 May;36(5):797-801.

Abstract

BACKGROUND

Oxaliplatin is the third-generation platinum complex to be active in advanced colorectal cancer. In Japan, it was approved in April 2005. FOLFOX regimen(a combination of leucovorin and fluorouracil with oxaliplatin) has been one of the standard chemotherapy regimens for metastatic colorectal cancer.

METHODS

To evaluate the efficacy and feasibility of FOLFOX4 and mFOLFOX6 regimens as first-line chemotherapy in Japanese patients with metastatic colorectal cancer, 23 consecutive patients with histologically confirmed colorectal cancer who were treated between June 2005 and August 2007 were investigated in this retrospective study. FOLFOX4 was used for treatment in 13 patients(57%), and mFOLFOX6 was in 10 patients(43%).

RESULTS

The objective response rate was 50.0%. The median survival time was 17.4 months. The median number of cycles was 8.0, with a median relative dose intensity of 74.5% for oxaliplatin. Grade 3 or 4 hematological toxicities were leukocytopenia in four patients, and neutropenia in 12 patients, while non-hematological toxicities such as nausea, anorexia and sensory neuropathy occurred in only one patient each adverse event. No treatment-related deaths occurred.

CONCLUSION

FOLFOX regimen has good efficacy in Japanese patients with metastatic colorectal cancer as first-line chemotherapy, with an acceptable overall toxicity profile.

摘要

背景

奥沙利铂是第三代对晚期结直肠癌有效的铂类复合物。在日本,它于2005年4月获批。FOLFOX方案(亚叶酸钙、氟尿嘧啶与奥沙利铂联合使用)一直是转移性结直肠癌的标准化疗方案之一。

方法

为评估FOLFOX4和mFOLFOX6方案作为日本转移性结直肠癌患者一线化疗的疗效和可行性,在这项回顾性研究中,对2005年6月至至2007年8月期间连续治疗的23例经组织学确诊的结直肠癌患者进行了调查。13例患者(57%)接受FOLFOX4治疗,10例患者(43%)接受mFOLFOX6治疗。

结果

客观缓解率为50.0%。中位生存时间为17.4个月。中位周期数为8.0,奥沙利铂的中位相对剂量强度为74.5%。3级或4级血液学毒性为4例白细胞减少和12例中性粒细胞减少,而非血液学毒性如恶心、厌食和感觉神经病变各仅发生在1例患者中。未发生与治疗相关的死亡。

结论

FOLFOX方案作为日本转移性结直肠癌患者的一线化疗具有良好疗效,总体毒性可接受。

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