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BIBW 2992 as add-on to Gem/Cis in Advanced Biliary Tract Cancer

2019年8月26日 更新者:PD Dr Markus Möhler、Johannes Gutenberg University Mainz

Open-label, Uncontrolled, Multicenter Phase I/Ib Trial to Investigate Safety and Efficacy of BIBW 2992 and Standard Gemcitabine/Cisplatin in Chemo-naïve Patients With Advanced Biliary Tract Adenocarcinoma

An open-label, uncontrolled, multicenter phase I/Ib trial to investigate safety and efficacy of BIBW 2992 added to the standard therapy of Gemcitabine/Cisplatin in chemo-naïve patients with advanced and/or metastatic adenocarcinoma of the biliary tract

研究概览

地位

终止

干预/治疗

详细说明

The primary objective is safety and toxicity, including maximum tolerated dose, of BIBW 2992 when given as add-on therapy to Gem/Cis.

研究类型

介入性

注册 (实际的)

9

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Mainz、德国、55131
        • I. Medizinische Klinik und Poliklinik der Universitätsmedizin

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Male and female patients aged ≥ 18 years
  • Signed and dated written informed consent,
  • Histologically confirmed adenocarcinoma of the gallbladder or intrahepatic bile ducts or extrahepatic bile ducts (metastasized) or histologically proven hepatic metastases of an earlier resected and histologically proven biliary tract cancer or a Klatskin tumour (hilar cholangiocarcinoma)

    • with pain and biliary obstruction controlled
    • adequate biliary drainage, no uncontrolled infection
    • ECOG Performance Status of 0-1
    • LFTs: bilirubin (total) ≤ 1.5 x ULN, ALT/ AST/ alkaline phosphatase ≤ 3 2.5 x ULN (≤ 5 x ULN if liver metastases are present)
    • No prior systemic treatment i) previous adjuvant chemotherapy is allowed (completed ≥ 6 months if containing Gemcitabine or platinum salts); ii) previous irradiation (external radiotherapy, brachytherapy, chemoembolization) and PDT are allowed, provided that there is still at least one unidimensionally measurable target lesion in an untreated area
  • Resolution of all side effects of prior surgical procedures to CTCAE grade ≤ 1 (except for the laboratory values specified below)
  • At least 4 weeks from any major surgery (at first dose of study drug)
  • Life expectancy of at least 12 weeks.
  • Cardiac left ventricular function with resting ejection fraction (LVEF) ≥ 50%
  • Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to start of therapy:

    • Haemoglobin > 10.0 g/dl (=6.2 mmol/l), blood transfusion is allowed
    • Absolute neutrophil count (ANC) > 1,500/mm3 (=1.5x 109/L)
    • Platelet count ≥ 100,000/μl (=100x 109/L)
    • Total bilirubin ≤ 1.5 times the upper limit of normal
    • ALT and AST ≤ 2.5 x institutional upper limit of normal (in case of liver metastases: ALT and AST ≤ 5 x institutional upper limit of normal)
    • Prothrombin rate > 60% or INR < 1.5

Main exclusion criteria

  • Large surgery (except diagnostic biopsy) or smaller surgical procedures, external radiotherapy, brachytherapy, or PDT within 30 days prior to start of treatment.
  • Other tumor type than adenocarcinoma (e.g. leiomyosarcoma, lymphoma) or a second cancer except in patients with squamous or basal cell carcinoma of the skin or carcinoma in situ of the cervix which has been effectively treated.
  • History of acute cardiac disease: congestive heart failure > NYHA class 2; active CAD (MI more than 6 months prior to study entry is allowed);
  • Patients on immunosuppressant therapy or with known HIV infection
  • Active clinically serious infections (> grade 2 NCI-CTC version 3.0)
  • History of organ allograft
  • Pregnant or breast-feeding patients.
  • Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation
  • Any condition that is unstable or could jeopardize the safety of the patient and their compliance in the study
  • Gastrointestinal (GI) tract disease resulting in an inability to take oral medication or a requirement for IV alimentation, prior surgical procedures affecting absorption, or active peptic ulcer disease
  • History of pre-existing interstitial lung disease (ILD)
  • Patients with untreated or symptomatic brain metastases.
  • Persistent Grade 2 or greater neurotoxicity / neuropathy from any cause

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Dose level 1 (Part A)
30 mg BIBW 2992, Gemcitabin (1.000 mg/m² BSA i.v.)/Cisplatin (25 mg/m² BSA i.v.)
once daily per os
其他名称:
  • Gemcitabine and Cisplatin
实验性的:Dose level -1 (Part A)
30 mg BIBW 2992, Gemcitabin (800 mg/m² BSA i.v.)/Cisplatin (20 mg/m² BSA i.v.)
once daily per os
其他名称:
  • Gemcitabine and Cisplatin

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Number of Adverse Events
大体时间:Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.

In part A the maximum tolerated dose (MTD) of BIBW 2992 administered continuously to the standard therapy of Gemcitabine / Cisplatin (Gem/Cis) (administered together on day 1 and 8 of a three-week cycle) will be evaluated in a 2 step dose escalation.

Safety and toxicity will be evaluated as described and considered primary for part B of the study.

Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.

次要结果测量

结果测量
措施说明
大体时间
Time to Progress (TTP)
大体时间:Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
Median time to progress (according to RECIST 1.1 criteria) including the 95% confidence intervals were determined using Kaplan-Meier estimates. Time from start of treatment to first documentation of objective tumour progression. Deaths were censored at the time of death.
Treatment period: up to eight cycles (maximum 8 months). 12 months follow-up period.
Overall Survival (OS)
大体时间:Time from start of treatment to death due to any cause. Time to last observation will be used if a patient has not died and OS for the patient will be considered censored. Estimated time period: up to 76 weeks
Median overall survival time including the 95% confidence interval were determined using Kaplan-Meier estimates.
Time from start of treatment to death due to any cause. Time to last observation will be used if a patient has not died and OS for the patient will be considered censored. Estimated time period: up to 76 weeks
Objective Response Rate
大体时间:Treatment period: up to eight cycles (maximum 8 months).
Response was assessed by means of RECIST 1.1 criteria for target lesions, non-target lesions and the appearance of new lesions. Objective response was defined as the CR, PR or SD at end of treatment
Treatment period: up to eight cycles (maximum 8 months).
Tumor Control Rate
大体时间:Treatment period: up to eight cycles (maximum 8 months).
Tumor control rate is defined as the best tumour response (confirmed partial or complete response, stable disease) that is achieved until end of treatment according to Recist 1.1.
Treatment period: up to eight cycles (maximum 8 months).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Markus Moehler, Prof. Dr. med.、University Medical Center of the Johannes Gutenberg-University Mainz

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年8月1日

初级完成 (实际的)

2016年4月1日

研究完成 (实际的)

2016年4月1日

研究注册日期

首次提交

2012年8月17日

首先提交符合 QC 标准的

2012年8月31日

首次发布 (估计)

2012年9月6日

研究记录更新

最后更新发布 (实际的)

2019年9月6日

上次提交的符合 QC 标准的更新

2019年8月26日

最后验证

2019年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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