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S-1 联合伊立替康和奥沙利铂一线治疗转移性结直肠癌患者:一项前瞻性 II 期研究和遗传药理学分析。

S-1 plus irinotecan and oxaliplatin for the first-line treatment of patients with metastatic colorectal cancer: a prospective phase II study and pharmacogenetic analysis.

机构信息

Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang 410-769, Korea.

出版信息

Br J Cancer. 2013 Sep 17;109(6):1420-7. doi: 10.1038/bjc.2013.479. Epub 2013 Aug 20.

DOI:10.1038/bjc.2013.479
PMID:23963147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3776990/
Abstract

BACKGROUND

S-1 is an oral fluoropyrimidine that mimics infusional 5-fluorouracil. The aim of this phase II trial was to explore the clinical efficacy of the triplet regimen TIROX, which consists of S-1, irinotecan and oxaliplatin.

METHODS

Forty-two chemo-naive patients with metastatic colorectal cancer (mCRC) were planned to be enrolled and be treated with irinotecan 150 mg m(-2) followed by oxaliplatin 85 mg m(-2) on day 1 and S-1 80 mg m(-2) per day from day 1 to 14 every 3 weeks. Polymorphisms in the UGT1A1, UGT1A6, UGT1A7 and CYP2A6 genes were analysed.

RESULTS

Between July 2007 and February 2008, 43 patients were enrolled. An objective response was noted in 29 patients (67.4%, 95% confidence interval: 53.4-81.4), of which 2 achieved durable complete responses. The median progression-free survival was 10.0 months and the median overall survival was 19.2 months. Significant grade 3 or 4 adverse events were neutropenia (45.2%), febrile neutropenia (9.5%), diarrhoea (7.1%) and vomiting (9.5%). Increased gastrointestinal toxicities were associated with the presence of UGT1A62 or UGT1A73 and an improved tumour response was noted in those without variant alleles of CYP2A6 or UGT1A1*60.

CONCLUSION

The combination of S-1, irinotecan and oxaliplatin showed favourable efficacy and tolerability in untreated patients with mCRC.

摘要

背景

S-1 是一种模拟持续输注氟尿嘧啶的口服氟嘧啶类药物。本 II 期试验旨在探索 S-1、伊立替康和奥沙利铂三联方案 TIROX 的临床疗效,该方案由 S-1、伊立替康和奥沙利铂组成。

方法

计划招募 42 例初治转移性结直肠癌(mCRC)患者,接受伊立替康 150mg/m2 静脉滴注,随后奥沙利铂 85mg/m2 静脉滴注,第 1 天;S-1 80mg/m2,每天 1 次,从第 1 天到第 14 天,每 3 周 1 次。分析 UGT1A1、UGT1A6、UGT1A7 和 CYP2A6 基因的多态性。

结果

2007 年 7 月至 2008 年 2 月期间,共招募 43 例患者。29 例(67.4%,95%置信区间:53.4-81.4)患者观察到客观缓解,其中 2 例获得持久完全缓解。中位无进展生存期为 10.0 个月,中位总生存期为 19.2 个月。显著的 3 级或 4 级不良事件有中性粒细胞减少症(45.2%)、发热性中性粒细胞减少症(9.5%)、腹泻(7.1%)和呕吐(9.5%)。胃肠道毒性增加与 UGT1A62 或 UGT1A73 有关,而 CYP2A6 或 UGT1A1*60 无变异等位基因的患者肿瘤反应改善。

结论

S-1、伊立替康和奥沙利铂联合治疗初治 mCRC 患者疗效良好,耐受性好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/5225e3606905/bjc2013479f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/37050a3b0eb4/bjc2013479f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/e5bb9db5dfa2/bjc2013479f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/5225e3606905/bjc2013479f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/37050a3b0eb4/bjc2013479f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/e5bb9db5dfa2/bjc2013479f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/3776990/5225e3606905/bjc2013479f3.jpg

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