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临床试验/NCT04692051
NCT04692051Unknown2 期

A Phase II Study for Nab-paclitaxel Plus Cisplatin vs Gemcitabine Plus Cispatin as First Line Chemotherapy in Advanced Biliary Tract Cancer

Huazhong University of Science and Technology1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
100
试验地点
1
主要终点
PFS

研究概览

简要总结

It is a trial to compare the efficacy and safety of Nab-paclitaxel plus Cisplatin vs Gemcitabine plus Cispatin as first line chemotherapy in advanced biliary tract cancer.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18 to 70 years;
  • Diagnosis of unresectable or recurrent or metastatic biliary tract cancer (Ampulla of Vater, gallbladder, intra or extra-hepatic biliary ducts);
  • Adequate bone marrow, liver and kidney function: absdute neutrophil count (ANC) ≥ 1.5 x 10^9/L, platelet count (PLT) ≥75 x 10^9/L, hemoglobin (HB) ≥ 75 g/L, White blood cell(WBC) ≥ 3.0 x 10^9/L, no bleeding symptoms or bleeding tendency; Total bilirubin (TBIL) ≤ 3 x upper limit of normal range (ULN), alanine glutamate transaminase (ALT) and glutamate transaminase (AST) ≤ 5 x upper limit of normal range (ULN); creatinine(Cr) ≤ 1.5 x upper limit of normal range(ULN) or creatinine clearance rate(CCR)≥ 45ml/min;
  • At least one measurable lesion;
  • Karnofsky Performance Status(KPS) ≥ 70;
  • Estimated life expectancy of at least 3 months;
  • Resolution of all acute clinical toxic effects of any prior treatment to grade ≤ 1, with the exception of alopecia;
  • Be able to understand and willingness to sign IRB-approved informed consent; (If the patient cannot sign the informed consent due to consciousness disorder, upper limbs paralysis or inability to write, the legal representative shall sign the informed consent on behalf of the patient).

排除标准

  • Ongoing uncontrolled infections, or have received systemic antibiotic therapy within 72 hours prior to registration;
  • Myeloproliferative disorder or any other hematopoietic function disorder;
  • Have an untreated second malignancy or brain metastasis;
  • Allergic to the chemotherapy drugs of this protocol;
  • Unable to cooperate due to neurologic diseases or psychiatric illness;
  • Pregnant or lactating female patients; Women of child-bearing age who refuse to accept contraceptive measures;
  • Have other significant medical illness, for example,active tuberculosis, active pneumonia, uncorrected electrolyte disturbance, uncontrolled tumor associated pain, uncontrolled hydrothorax or seroperitoneum and so on;
  • Patients need to receive other antitumor therapy at the same time;
  • Have received any other experimental treatment or participated in another interventional clinical trial within 30 days prior to registration;
  • Any other situation that the researcher considered patients are unsuitable for the trial.

研究组 & 干预措施

Nab-paclitaxel + Cisplatin

Experimental

Patients in this arm receive chemotherapy with Nab-paclitaxel plus Cisplatin

干预措施: Nab-paclitaxel + Cisplatin (Drug)

Gemcitabine + Cisplatin

Active Comparator

Patients in this arm receive chemotherapy with Gemcitabine plus Cisplatin

干预措施: Gemcitabine + Cisplatin (Drug)

结局指标

主要结局

PFS

时间窗: up to 3 years

PFS is defined as time from the start of treatment to progression of disease or death.

次要结局

  • OS(up to 3 years)
  • AEs(up to 3 years)
  • TTP(up to 3 years)
  • ORR(up to 3 years)

研究者

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

Xianglin Yuan

Professor, Head of the cancer center

Huazhong University of Science and Technology

研究点 (1)

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