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临床试验/NL-OMON50269
NL-OMON50269招募中2 期

eoadjuvant capecitabine, oxaliplatin, docetaxel and atezolizumab in non-metastatic, resectable gastric and GE-junction cancer. ;The PANDA trial - The PANDA trial

ederlands Kanker Instituut0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Primary resectable, gastro-oesophageal junction adenocarcinoma or gastric
  • adenocarcinoma
  • - WHO performance status of 0 or 1
  • - No distant metastases
  • - CT-scan < 4 weeks to registration
  • - Patients must be willing to undergo esophagogastroscopy and biopsies prior to
  • start of treatment and during treatment at set timepoints

排除标准

  • - Clinical symptoms or radiological suspicion of perforation
  • - Active auto-immune disease or documented history of autoimmune disease, or
  • other medical conditions requiring systemic steroid or immunosuppressive
  • medications, except for subjects with vitiligo, diabetes mellitus type 1,
  • residual hypothyroidism due to autommune condition only requiring hormone
  • replacement, psoriasis or resolved childhood asthma/atopy not requiring
  • systemic treatment
  • - Conditions requiring systemic treatment with either corticosteroids (>10mg
  • daily prednisone equivalents or other immunosuppressive medications within 14
  • days of study drug administration. Inhaled or topical steroids and adrenal
  • replacement doses > 10 mg daily prednisone equivalents are permitted in the
  • absence of active autoimmune disease;
  • - Previous treatment with immune checkpoint inhibitors
  • - History of allergy to study drug components, hypersensitivity reaction to any
  • monoclonal antibody
  • - Positive test for hepatitis B surface antigen (HBsAg) or hepatitis C virus
  • ribonucleic acid (HCV antibody) indicating acute or chronic infection;
  • - History of testing positive human immunodeficiency virus or known acquired
  • immunodeficiency syndrome (AIDS)
  • - Malignancies other than disease under study within 3 years prior to
  • inclusion, requiring systemic treatment or judged by the investigators to be
  • incompatible with the study, except for non-melanoma skin cancer.

研究者

发起方
ederlands Kanker Instituut

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