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临床试验/JPRN-UMIN000009101
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Feasibility study of CBDCA+TS-1 adjuvant therapy for p-stage IB(T2a>4cm)/II/IIIA non-small cell lung cancer - Feasibility study of CBDCA+TS-1 adjuvant therapy for non-small cell lung cancer

Osaka University Graduate School of Medicine0 个研究点目标入组 35 人开始时间: 2012年10月12日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
35

研究概览

简要总结

The adjuvant chemotherapy completion rate was 85.3% (29/34); 17/34 (50%) patients completed 4 courses without dose reduction. There were no treatment-related deaths, and Grade 3/4 adverse events included neutropenia (38.2%), leukocytopenia (14.7%), anemia (20.6%), thrombocytopenia (20.6%), anorexia (5.9%), fatigue (5.9%), and oral mucositis (2.9%). Two-year overall and disease-free survival rates were 96.3% and 53.3%, respectively. Adjuvant chemotherapy with carboplatin plus S-1 is safe and feasible.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Allergy for CBDCA/TS-1 Myocardial infarction within 6 months Interstitial pneumonia sever heart disease significant psychological disease uncontrollable diabetes mellitus

研究者

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