Phase III Randomized Controlled Trial of Adjuvant Capecitabine/Cisplatin Chemotherapy and Chemoradiation Therapy for Gastric Adenocarcinoma
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 458
- 试验地点
- 1
- 主要终点
- disease free survival
研究概览
简要总结
The objective of the trial is to compare disease-free survival between adjuvant capecitabine/cisplatin alone vs capecitabine/cisplatin with radiotherapy (chemoradiation) in curatively resected gastric cancer patients.
详细描述
Although gastrectomy is the only potentially curative treatment in gastric cancer patients, the overall survival results remain unsatisfactory. The main factor accounting for high mortality rate is the relapse after surgical resection. During the past few decades, the principle of combined modality treatment has been developed and applied in practice for various solid tumors and gastric cancer has not been an exception. In an attempt to prevent recurrence and increase the cure rate of gastric cancer patients after surgery, multiple studies using variable modalities have been undertaken. One of the landmark study in adjuvant trials was the Intergroup study INT-0116, which reported a significant improvement in survival with the use of chemoradiation therapy after gastric resection of stage Ib to IV gastric cancers. Thereafter, the chemoradiation therapy has gained popularity and has been increasingly recognized as a standard of care in U.S. Nevertheless, the result from INT-0116 study has been challenged by the fact that the surgical treatment applied in the trial was gastrectomy with limited lymph node dissection (D0 or D1) in 90% of cases. Therefore, it is debatable whether adjuvant chemoradiation therapy can confer survival benefit in patients with extensive lymph node dissection.
It is still disputable if chemoradiotherapy after D2 can improve the results of D2 alone. Thus, the assessment of the effect of adjuvant chemoradiotherapy in D2 resected gastric cancer is essential.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically proven gastric adenocarcinoma
- •≥ D2 resection
- •Stage IB(T1N1,T2bN0), II, IIIA, IIIB, IV(T4,N3 포함, M1 lymph node 제외)
- •18 ≤ age ≤ 75
- •No distant metastasis
- •Adequate bone marrow functions (ANC ≥ 1,500/ul, blood platelet ≥ 100,000/ul, haemoglobin ≥ 10g/dl)
- •Adequate renal functions(serum creatinine ≤ 1.5mg/dl)
- •liver functions (serum bilirubin ≤ 1.5mg/dl, AST/ALT ≤ 3 times(normal value)
- •Written informed consent
排除标准
- •Previous history of immunotherapy, chemotherapy, radiotherapy for gastric cancer
- •Active infection requiring antibiotics
- •Pregnant, lactating women
- •Psychiatric illness, epileptic disorders
- •Concurrent systemic illness not appropriate for chemotherapy
- •Resection margin (+)
- •Pathologic stage IA
- •History of other malignancy within 5 years except for non-melanoma skin cancer, cervix in situ carcinoma
- •M1 lymph node (+)
- •D0, D1 resection
研究组 & 干预措施
capecitabine/cisplatin/radiotherapy
postoperative XP/RT
干预措施: Capecitabine, cisplatin, Radiotherapy (+/-) (Drug)
capecitabine/cisplatin
postoperative XP
干预措施: Capecitabine, cisplatin, Radiotherapy (+/-) (Drug)
结局指标
主要结局
disease free survival
时间窗: 3-year
次要结局
未报告次要终点
研究者
Won Ki Kang
Professor of Medicine, Sungkyunkwan University School of Medicine, Department of Hematology and Oncology
Samsung Medical Center
