Suppr超能文献

晚期胃癌患者 S-1 单药治疗失败后采用伊立替康联合顺铂进行二线化疗。

Second-line chemotherapy with irinotecan plus cisplatin after the failure of S-1 monotherapy for advanced gastric cancer.

机构信息

Gastrointestinal Oncology Division, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Gastric Cancer. 2010 Aug;13(3):186-90. doi: 10.1007/s10120-010-0557-0. Epub 2010 Sep 5.

Abstract

BACKGROUND

For advanced gastric cancer (AGC), second-line chemotherapy after the failure of S-1 has not yet been established. The present study aimed to retrospectively evaluate the efficacy and safety of irinotecan plus cisplatin (IP) therapy after the failure of S-1 in patients with AGC.

METHODS

The subjects included 87 patients with AGC who received IP therapy as second-line chemotherapy. Irinotecan (70 mg/m(2)) was administered by intravenous infusion followed by an intravenous infusion of cisplatin (80 mg/m(2)) on day 1. On day 15, irinotecan (70 mg/m(2)) alone was administered. The treatment was repeated every 4 weeks until disease progression, patient refusal, or severe adverse events.

RESULTS

The median patient age was 62 years (range, 39-75 years), and the median number of treatment cycles was 3 (range, 1-9). Out of the 87 patients, 70 were assessable for clinical response. There were 2 complete responses and 18 partial responses. The overall response rate was 28.6% (95% confidence interval [CI], 18.4%-40.6%) and the disease control ratio was 70.0%. The median time to progression and median survival time from the first day of IP therapy were 4.3 months and 9.4 months, respectively. The 1-year survival rate was 34.6%. Severe (grade 3/4) leukopenia, neutropenia, anemia, and thrombocytopenia were observed in 34%, 40%, 28%, and 8% of patients, respectively. Grade 3/4 nonhematologic toxicities included anorexia (17%), febrile neutropenia (10%), diarrhea (6%), fatigue (5%), nausea (2%), and elevated creatinine (1%).

CONCLUSIONS

The combination of irinotecan plus cisplatin as second-line chemotherapy for AGC appears to be an effective and feasible treatment option after S-1 failure.

摘要

背景

对于晚期胃癌(AGC),S-1 治疗失败后的二线化疗尚未确立。本研究旨在回顾性评估 S-1 治疗失败后接受伊立替康联合顺铂(IP)治疗的 AGC 患者的疗效和安全性。

方法

本研究纳入了 87 例接受 IP 作为二线化疗的 AGC 患者。伊立替康(70mg/m2)静脉滴注,随后第 1 天静脉滴注顺铂(80mg/m2)。第 15 天,单独给予伊立替康(70mg/m2)。每 4 周重复治疗,直至疾病进展、患者拒绝或出现严重不良事件。

结果

中位患者年龄为 62 岁(范围,39-75 岁),中位治疗周期数为 3 个(范围,1-9 个)。87 例患者中,70 例可评估临床反应。完全缓解 2 例,部分缓解 18 例。总缓解率为 28.6%(95%置信区间[CI],18.4%-40.6%),疾病控制率为 70.0%。从 IP 治疗第 1 天开始,中位无进展生存期和中位总生存期分别为 4.3 个月和 9.4 个月。1 年生存率为 34.6%。严重(3/4 级)白细胞减少、中性粒细胞减少、贫血和血小板减少分别见于 34%、40%、28%和 8%的患者。3/4 级非血液学毒性包括厌食(17%)、发热性中性粒细胞减少(10%)、腹泻(6%)、乏力(5%)、恶心(2%)和肌酐升高(1%)。

结论

伊立替康联合顺铂作为 S-1 治疗失败后二线化疗方案治疗 AGC 似乎是一种有效且可行的治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验