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回顾性研究一线联合化疗治疗晚期结直肠癌:韩国单中心经验。

A retrospective study of first-line combination chemotherapy in advanced colorectal cancer: a Korean single-center experience.

机构信息

Division of Hematology and Oncology, Department of Medicine, Dankook University Hospital, Dankook University College of Medicine, Cheonan, Korea.

出版信息

Cancer Res Treat. 2011 Jun;43(2):96-101. doi: 10.4143/crt.2011.43.2.96. Epub 2011 Jun 30.

Abstract

PURPOSE

Fluoropyrimidine-based combination chemotherapy, in combination with either oxaliplatin or irinotecan, has demonstrated efficacy and tolerability in treatment of advanced colorectal cancer (ACC).

MATERIALS AND METHODS

Between January 2006 and December 2007, a total of 478 ACC patients were treated with combination chemotherapy in first-line settings. Combination therapies included: 5-fluorouracil, folinic acid plus oxaliplatin (FOLFOX, n=172), 5-fluorouracil, folinic acid plus irinotecan (FOLFIRI, n=95), capecitabine plus oxaliplatin (XELOX, n=155), and capecitabine plus irinotecan (XELIRI, n=56). FOLFOX and FOLFIRI were repeated every 2 weeks, whereas XELOX and XELIRI were repeated every 3 weeks until occurrence of disease progression or unacceptable toxicity, or until a patient chose to discontinue treatment.

RESULTS

The median age was 58 years (range, 19 to 84 years) and the median chemotherapy durations for FOLFOX, FOLFIRI, XELOX, and XELIRI were 4.9, 4.5, 5.7, and 5.4 months, respectively. Combination chemotherapy regimens were generally well tolerated. The estimated median progression-free-survival (PFS) for all patients was 6.8 months (95% confidence interval, 6.3 to 7.3 months). No statistically significant difference in PFS was found among regimens used as first-line chemotherapy. Sixty percent (n=290) of patients received second or further lines of therapy after failure.

CONCLUSION

Fluoropyrimidine-based combination chemotherapy regimens appear to be equally active and tolerable as first-line therapy for ACC.

摘要

目的

氟嘧啶类联合化疗联合奥沙利铂或伊立替康在治疗晚期结直肠癌(ACC)方面显示出疗效和耐受性。

材料和方法

2006 年 1 月至 2007 年 12 月,478 例 ACC 患者在一线治疗中接受联合化疗。联合治疗方案包括:5-氟尿嘧啶、亚叶酸钙加奥沙利铂(FOLFOX,n=172)、5-氟尿嘧啶、亚叶酸钙加伊立替康(FOLFIRI,n=95)、卡培他滨加奥沙利铂(XELOX,n=155)和卡培他滨加伊立替康(XELIRI,n=56)。FOLFOX 和 FOLFIRI 每 2 周重复一次,而 XELOX 和 XELIRI 每 3 周重复一次,直到疾病进展或无法耐受毒性,或直到患者选择停止治疗。

结果

中位年龄为 58 岁(范围,19 至 84 岁),FOLFOX、FOLFIRI、XELOX 和 XELIRI 的中位化疗持续时间分别为 4.9、4.5、5.7 和 5.4 个月。联合化疗方案总体耐受性良好。所有患者的估计中位无进展生存期(PFS)为 6.8 个月(95%置信区间,6.3 至 7.3 个月)。作为一线化疗,不同方案的 PFS 无统计学差异。60%(n=290)的患者在失败后接受了二线或进一步的治疗。

结论

氟嘧啶类联合化疗方案作为 ACC 的一线治疗似乎同样有效且耐受良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdec/3138923/69dd2458d64c/crt-43-96-g001.jpg

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