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临床试验/NCT03143153
NCT03143153已完成3 期

A Randomized Phase 3 Study of Nivolumab Plus Ipilimumab or Nivolumab Combined With Fluorouracil Plus Cisplatin Versus Fluorouracil Plus Cisplatin in Subjects With Unresectable Advanced, Recurrent or Metastatic Previously Untreated Esophageal Squamous Cell Carcinoma

Bristol-Myers Squibb190 个研究点 分布在 9 个国家目标入组 970 人开始时间: 2017年6月29日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
970
试验地点
190
主要终点
Overall Survival (OS) in Participants With Tumor Cell PD-L1

研究概览

简要总结

The main purpose of this study is to compare how long subjects with esophageal cancer live overall or live without disease progression after receiving nivolumab and ipilimumab or nivolumab combined with fluorouracil plus cisplatin versus fluorouracil plus cisplatin

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Must have histologically confirmed squamous cell carcinoma or adenosquamous cell carcinoma of esophagus
  • Male or Female at least 18 years of age
  • Must have esophageal cancer that cannot be operated on, or treated with definitive chemoradiation with curative intent, that is advanced, reoccurring or has spread out
  • Must have full activity or, if limited, must be able to walk and carry out light activities such as light house work or office work
  • Must agree to provide tumor tissue sample, either from a previous surgery or biopsy within 6 months or fresh, prior to the start of treatment in this study

排除标准

  • Presence of tumor cells in the brain or spinal cord which are symptomatic or require treatment
  • Active known or suspected autoimmune disease
  • Any serious or uncontrolled medical disorder or active infection
  • Known history of positive test for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS)
  • Any positive test result for hepatitis B or C indicating acute or chronic infection and/or detectable virus
  • Other protocol defined inclusion/exclusion criteria apply

研究组 & 干预措施

Nivolumab + Cisplatin + Fluorouacil

Experimental

干预措施: Cisplatin (Drug)

Nivolumab + Ipilimumab

Experimental

干预措施: Nivolumab (Biological)

Nivolumab + Ipilimumab

Experimental

干预措施: Ipilimumab (Biological)

Nivolumab + Cisplatin + Fluorouacil

Experimental

干预措施: Nivolumab (Biological)

Nivolumab + Cisplatin + Fluorouacil

Experimental

干预措施: Fluorouracil (Drug)

Cisplatin + Fluorouracil

Active Comparator

干预措施: Cisplatin (Drug)

Cisplatin + Fluorouracil

Active Comparator

干预措施: Fluorouracil (Drug)

结局指标

主要结局

Overall Survival (OS) in Participants With Tumor Cell PD-L1

时间窗: From the date of randomization to up to the date of death (up to approximately 20 months)

Overall Survival (OS) is defined as the time between the date of randomization and the date of death. For participants without documentation of death, OS will be censored on the last date the subject was known to be alive.

Progression-free Survival (PFS) as Assessed by BICR in Participants With Tumor Cell PD-L1

时间窗: From the date of randomization to up to the date of the first documented disease progression or death (up to approximately 9 months)

Progression-free survival (PFS) is defined as the time from randomization to the date of the first documented progressive disease (PD) per Blinded Independent Central Review (BICR) or death due to any cause. Participants who die without a reported prior PD per BICR (and die without start of subsequent therapy) will be considered to have progressed on the date of death. Participants who did not have documented PD per BICR per RECIST1.1 criteria and who did not die, will be censored at the date of the last evaluable tumor assessment on or prior to initiation of the subsequent anti-cancer therapy. Participants who did not have any on-study tumor assessments and did not die (or died after initiation of the subsequent anti-cancer therapy) will be censored at the randomization date. Participants who started any subsequent anti-cancer therapy without a prior reported PD per BICR will be censored at the last tumor assessment on or prior to initiation of the subsequent anti-cancer therapy.

次要结局

  • Overall Survival (OS) in All Randomized Participants(From the date of randomization to up to the date of death (up to approximately 88 months))
  • Progression-free Survival (PFS) in All Randomized Participants as Assessed by BICR(From the date of randomization to up to the date of the first documented disease progression or death (up to approximately 88 months))
  • Objective Response Rate (ORR) as Assessed by BICR(From the date of randomization to up to the date of objectively documented progression or the date of subsequent anti-cancer therapy, whichever occurs first (up to 88 months))

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (190)

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