Phase II Study of Best Support Care (BSC) Plus ZD6474(Vandetanib) in Patients With Inoperable Hepatocellular Carcinoma (HCC)

Carcinoma, Hepatocellular Clinical Trial

Official title:

A Randomised, Double-blind, Parallel Group, Multi-centre, Phase II Study to Assess the Efficacy and Safety of Best Support Care (BSC) Plus ZD6474(Vandetanib) 300 mg, BSC Plus ZD6474(Vandetanib) 100 mg, and BSC Plus Placebo in Patients With Inoperable Hepatocellular Carcinoma (HCC)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00508001
• Other study ID #: D4200C00072
• Status: Completed
• Phase: Phase 2
• First received: July 25, 2007
• Last updated: June 12, 2012
• Start date: July 2007
• Est. completion date: June 2009

Study information

• Verified date: June 2012
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Health authority: Taiwan: Department of Health
• Study type: Interventional

Clinical Trial Summary

This is a multi-centre, phase II study to assess the efficacy and safety of ZD6474 in patients with Child-Pugh class A, inoperable HCC. This study comprises 2 phases, the primary treatment phase and the secondary treatment phase. The primary treatment phase is a randomised, double-blind, parallel-group phase II study to assess the efficacy and safety of ZD6474 300 mg plus best support care (BSC), ZD6474 100 mg plus BSC, and placebo plus BSC. The secondary treatment phase is an open-label expanded access program of ZD6474. In the primary treatment phase, patients will be randomised in a 1:1:1 ratio to receive ZD6474 300 mg plus BSC, ZD6474 100 mg plus BSC, or placebo plus BSC, respectively. Randomisation will be stratified on the basis of Cancer of the Liver Italian Programme (CLIP) tumour staging (CLIP score 0-2 versus 3-4). The primary treatment will continue until objective disease progression, according to Response Evaluation Criteria in Solid Tumours (RECIST) criteria, or until patients meet any other withdrawal or discontinuation criteria.The primary endpoint is tumour stabilisation rate, and the secondary endpoints are objective response rate, progression-free survival, and overall survival. The purpose of the secondary treatment phase is to expand the access of ZD6474 so that every patient who is enrolled into this study can have the chance to receive the active medicine.Once an individual patient has progressive disease in the primary treatment phase, the blind will be broken for this patient. If this patient is in the ZD6474 100 mg arm or placebo arm, the patient will be offered the secondary treatment with ZD6474 300 mg per day. If this patient is randomised to the ZD6474 300 mg arm, the study medication will be discontinued unless the patient wishes to remain the treatment, and the patient is to be followed up for survival.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 67
• Est. completion date: June 2009
• Est. primary completion date: November 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

• Able to understand and provide informed consent

• Histologically diagnosed HCC, OR clinically diagnosed HCC for patients with difficulty in obtaining histological diagnosis. A clinically diagnosed HCC should fulfil ALL the criteria below.

• Chronic hepatitis B or C and/or evidence of liver cirrhosis

• Presence of hepatic tumour(s) with image findings (sonography, CT scan, or MRI scan) compatible with HCC, and no evidence of other gastrointestinal tumours

• A persistent elevation of serum a-fetoprotein level >= 400 ng/ml without any evidence of an existing a-fetoprotein-secreting germ cell tumour

• Locally advanced (for example, portal vein invasion, multiple nodules, or nodules in both lobes) or metastatic HCC with at least one measurable lesion by RECIST criteria that meets ANY the criteria below:

• HCC not suitable to receive local therapy, including surgical resection, percutaneous ethanol injection (PEI), or transarterial chemo-embolization (TACE)

• Disease recurred or was refractory to previous local therapy

• Patients refused local therapy

• At least one measurable lesion by RECIST criteria. Tumour lesions treated previously with local radiotherapy, percutaneous ethanol injection, radiofrequency ablation, or transarterial embolization are NOT considered measurable.

• If they completed percutaneous ethanol injection, radiofrequency ablation, transarterial embolization, or cryotherapy at least 4 weeks prior to enrollment, patients must have subsequent progression or recurrence with at least one new measurable lesion that has not been treated with any local procedure.

• Karnofsky performance status >= 70

• Life expectancy >= 2 months

• Child-Pugh class A liver function

• Adequate bone marrow reserve, defined as white blood cell count >= 3,000/ml, and platelet count >= 75,000/ml

• Liver transaminases (AST and ALT) <= 5 times upper normal limits (UNLs); serum bilirubin <= 1.5 times UNL <= 2 mg/dL

• Serum creatinine <= 1.5 times UNL

• Negative pregnancy test for women of childbearing potential. Patients of childbearing age as well as his/her partner must use effective contraception during the study period unless they are surgically sterile or one year post-menopausal

Exclusion Criteria:

• Receiving concurrent anti-cancer therapy for HCC, which includes local therapy, chemotherapy, or other experimental therapy

• Prior systemic cytotoxic chemotherapy

• Prior transarterial chemo-embolization (TACE) or hepatic arterial infusion (HAI), with any of the following conditions for those patients who have any target lesions in the liver:

• More than 5 TACE or HAI sessions undergone prior to enrollment

• The cumulative doses of doxorubicin > 120 mg/m2, mitomycin-C > 24 mg/m2, cisplatin > 120 mg/m2, or 5-fluorouracil > 2400 mg/m2

• Details of the TACE or HAI regimens are not available in the chart

• (Note: The number of sessions of prior TACE or HAI will not be limited for patients who have no target lesion in the liver).

• Local treatment including radiotherapy (except palliative radiotherapy), percutaneous ethanol injection, radiofrequency ablation, transarterial embolization, or cryotherapy completed within 4 weeks prior to enrollment

• Prior therapy targeting VEGF or EGF signalling pathways, including but not limited to bevacizumab, cetuximab, gefitinib, erlotinib, or sorafenib.

• Prior thalidomide therapy is not allowed but for patients who stop thalidomide due to intolerability and meet either one of following condition can be included:

• Patients who took thalidomide for no more than <= 3 days before enrolment

• Patients who took thalidomide for > 3 days but <= 14 days and are confirmed clinically not responding to thalidomide. 14 days washout period is needed before enrolment.

• Laboratory results:

• Serum potassium less than 4.0 mmol/L despite supplementation

• Serum calcium (ionized or adjusted for albumin) or magnesium out of their normal ranges despite supplementation

• Esophagogastroduodenoscopy reveals lesions that are considered high risk of gastrointestinal bleeding

• Brain or leptomeningeal metastases

• History of HCC tumour rupture

• History of upper gastrointestinal bleeding within 1 year

• Current or recent (within 10 days prior to enrollment) users of full-dose oral or parenteral anti-coagulants

• Surgical procedures, open biopsy, or significant traumatic injury within 28 days prior to enrollment. Fine-needle aspiration, core biopsy, and central venous line placement must be done at least 7 days prior to enrollment. Incompletely healed surgical incision prior to enrollment.

• Evidence of severe or uncontrolled systemic disease or any concurrent condition which in the investigator's opinion makes it undesirable for the patient to participate in the study or which would jeopardize compliance with the protocol.

• Clinically significant cardiac event such as myocardial infarction; New York Heart Association classification of heart disease > 2 within 3 months before entry; or other cardiac disease that, in the opinion of the investigator, increases the risk of ventricular arrhythmia.

• History of arrhythmia (multifocal premature ventricular contractions, bigeminy, trigeminy, ventricular tachycardia, or uncontrolled atrial fibrillation), which is symptomatic, requires treatment (CTCAE grade 3), or asymptomatic sustained ventricular tachycardia. Atrial fibrillation, if controlled on medication, will not be excluded.

• Previous history of QTc prolongation as a result of therapy with other medication that required discontinuation of that medication.

• Congenital long QT syndrome, or first-degree relative with unexplained sudden death under 40 years of age

• Presence of left bundle branch block

• QTc with Bazett's correction that is unmeasurable, or >= 480 msec on screening ECG

• Use of any concomitant medication that are generally accepted by authorities to have a risk of causing Torsades de Pointes within 2 weeks before enrollment (use of the concomitant medication that may be associated with Torsades de Pointes but lack substantial evidence of causing Torsades de Pointes is allowed, but the screening QTc must be less then 460 msec, and an additional ECG is required within the first 24 hours after the first dose of study medication is required).

• Use of any concomitant medication that induce CYP3A4 activity within 2 weeks before enrollment

• Use of interferon within 3 months before enrollment

• Hypertension not well controlled by medical therapy (systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg)

• Currently active diarrhea that may affect the ability of the patient to absorb the ZD6474 or diarrhea due to intolerability

• Current pregnancy or breast-feeding

• Other previous or current malignancies within the last 5 years, with the exception of adequately treated cervical carcinoma in situ and basal cell or squamous cell carcinoma of the skin

• Receipt of any investigational agents within 30 days prior to commencing protocol treatment

• Any unresolved toxicity greater than CTC grade 2 from previous anti-cancer therapy

• Known hypersensitivity to ZD6474 or any of its excipients

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Hepatocellular

Intervention

Drug:
• Vandetanib
ZD6474 300mg
• Vandetanib
ZD6474 100 mg
• Best Supportive Care
Placebo + Best Supportive Care

Locations

Country	Name	City	State
Taiwan	Research Site	Tainan
Taiwan	Research Site	Taipei
Taiwan	Research Site	Taoyuan

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tumour Stabilisation Rate	Tumour stabilisation rate calculated as percentage of patients with best objective tumour response (Complete Response, Partial Response or Stable Disease) for >=16 weeks based on Response Evaluation Criteria in Solid Tumours (RECIST).; Complete Response - Disappearance of all target lesions; Partial Response - >=30% decrease in the sum of longest diameter of target lesions; Progressive Disease - >=20% increase in the sum of longest diameter of target lesions; Stable Disease - neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD.	After 16 weeks of treatment.	No
Secondary	Objective Response Rate	Objective Response rate defined as percentage of patients with Complete Response [CR] or Partial Response [PR] based on Response Evaluation Criteria in Solid Tumours (RECIST).; Partial response (PR) must have = 30% decrease in the sum of longest diameter of all target lesions as assessed by Magnetic Resonance Imaging (MRI). Complete response (CR) must have disappearance of all target and non-target lesions as assessed by MRI.	After 16 weeks of treatment.	No
Secondary	Progression-free Survival	Progression-free survival defined as the period from date of randomization(start of treatment) to date of disease progression or death.	from the date of randomisation to the date of documented disease progression or death for any cause	No
Secondary	Overall Survival	Overall survival defined as the time from randomization (start of treatment) until death from any cause.	assessed up to 360 days	No