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临床试验/jRCTs041220085
jRCTs041220085已完成不适用

Phase2 study of intrapatient dose-escalation of biweekly trifluridine/tipiracil + bevacizumab for patients with metastatic colorectal cancer refractory to standard therapies (E-BiTS study)

未提供0 个研究点目标入组 36 人开始时间: 2022年11月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
36
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • •Patients has been diagnosed with unresectable advanced or recurrent colorectal adenocarcinoma by histopathological diagnosis.
  • •The age of patients on registration date is 20 years or older.
  • •ECOG PS 0 or
  • •Patients have measurable lesions.
  • •Patients have a history of refractory or intolerant to the following chemotherapy.
  • •(1) All three drugs, fluorinated pyrimidine anticancer drug, oxaliplatin, and irinotecan
  • •(2) Angiogenesis inhibitor (bevacizumab, ramucirumab, or aflibercept)
  • •(3) Anti-EGFR antibody drug (cetuximab or panitumumab) in RAS wild type
  • •(4) BRAF inhibitor (encorafenib) in BRAF mutant
  • •(5) Immune checkpoint inhibitors (pembrolizumabor nivolumab) in MSI-H
  • •Patients who have not been treated with FTD/TPI.
  • •Patients who can take orally
  • •Patients are expected to live for 3 months or longer
  • •Patients whose latest test values within 14 days before registration meet all of the following.
  • •(1) Number of neutrophils >= 1500/mm3
  • •(2) Platelet count >= 75000/mm3
  • •(3) Total bilirubin <= 1.5 mg / dL
  • •(4) AST <= 100 U/L
  • •(5) ALT <= 100 U/L
  • •(6) Serum creatinine <= 1.5 mg/dL and Ccr >= 60mL/min
  • •(7) Urine protein (test paper method) 1+ or less, or UPC (Urine Protein Creatinine) ratio <= 2.0
  • •Patients have given written consent to participate in the study.

排除标准

  • •Patients with double cancers requiring chemotherapy (excluding hormone therapy)
  • •Patients have infectious diseases which need systemic treatment.
  • •Patients have difficulty in being enrolled in this study due to clinically problematic mental illness
  • •Patients with the following complications
  • •(1) Renal failure
  • •(2) Cirrhosis / liver failure
  • •(3) Chronic lung disease requiring oxygen administration
  • •(4) Concomitant with unstable angina (angina whose onset or seizures have worsened within the last 3 weeks) or a history of myocardial infarction within 6 months
  • •(5) Other complications that the doctor in charge considers to be serious
  • •Patients receiving continuous systemic administration of steroids or immunosuppressants
  • •Patients with unstable thromboembolism.
  • •Pregnant women, lactating women, women who may be pregnant now, or patients who are not willing to use contraception
  • •Patients judged by the investigator to be inappropriate

结局指标

主要结局

-

Disease control rate

次要结局

  • PFS
  • OS
  • RDI
  • RR
  • AE

研究者

发起方
未提供

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