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临床试验/EUCTR2021-001575-16-FR
EUCTR2021-001575-16-FR进行中(未招募)1 期

A multicenter open-label randomized controlled prospective phase II study evaluating the efficacy of Selective Internal Radiation Therapy (Yttrium-90 glass microspheres) combined with Capecitabine in the neoadjuvant setting of Operable intrahepatic CHOlangiocarcinoma - S7-PRODIGE-SIROCHO

Centre Régional de lutte contre le Cancer Eugène Marquis0 个研究点目标入组 62 人开始时间: 2021年9月2日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
62

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age > 18 years-old,
  • ECOG Performance Status <2
  • Histologically-proven ICC
  • No previous treatment,
  • Tumour deemed resectable by a hepatobiliary surgeon, validated by a Surgical Review Board,
  • Significant risk of close margins, defined as:
  • -Resection margin predicted by the surgeon <1cm
  • -Tumour > 5cm
  • -Multifocal lesion deemed resectable, validated by a Surgical Review Board
  • Patient information and signature of informed consent or legal representative.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 40
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 22

排除标准

  • Inadequate haematological, hepatic, renal and coagulation functions:
  • -Haemoglobin = 8,5 g/dl
  • -Neutrophils < 1,5 Giga/L
  • -Platelets < 60 Giga/L
  • -Bilirubin > 34 µmol/L
  • -ASAT/ALAT > 5 x ULN
  • -Creatinine clearance < 30 ml/min (MDRD)
  • -TP et INR > 2,3 ULN
  • -TCA > 1,5 x ULN
  • -Uracil blood level >16 ng/mL
  • Respiratory insufficiency,
  • Comorbidity precluding surgical resection, such as severe heart disease
  • Other invasive malignancies in the past 3 years,
  • Patient participate to an interventional study that tests another medical intervention before surgery.

研究者

发起方
Centre Régional de lutte contre le Cancer Eugène Marquis

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