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临床试验/NCT00323830
NCT00323830已完成3 期

Phase III Randomized Controlled Trial of Adjuvant Capecitabine/Cisplatin Chemotherapy and Chemoradiation Therapy for Gastric Adenocarcinoma

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 458 人开始时间: 2004年10月最近更新:
适应症
干预措施
相关药物

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

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

Experimental

postoperative XP/RT

干预措施: Capecitabine, cisplatin, Radiotherapy (+/-) (Drug)

capecitabine/cisplatin

Active Comparator

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

Won Ki Kang

Professor of Medicine, Sungkyunkwan University School of Medicine, Department of Hematology and Oncology

Samsung Medical Center

研究点 (1)

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