ZD6474 Alone and in Combination With Retinoic Acid in Pediatric Neuroblastoma - Full Text View

Sponsor:	M.D. Anderson Cancer Center
Collaborator:	AstraZeneca
Information provided by:	M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:	NCT00533169

Purpose

Hypothesis:

ZD6474 will have significant antitumor activity in cases of relapsed and refractory neuroblastoma due to the combined inhibition of biologically relevant RET, VEGFR, and EGFR pathways, and it will have synergistic antitumor activity in combination with retinoid therapy.

Primary Objective:

To determine the pharmacokinetics, safety, dose-limiting toxicities, and maximum tolerated dose of ZD6474, alone and in combination with retinoic acid, in patients with relapsed or refractory neuroblastoma.

Secondary Objective:

To assess progression-free survival (PFS) and objective tumor response rates in children with relapsed and refractory neuroblastoma treated with ZD6474 +/- retinoic acid in the context of a Phase I trial.

Exploratory Objectives:

To explore blood-based biomarkers before and after treatment with ZD6474 alone and in combination with retinoic acid.

To investigate the presence, activation, and functional status of target receptors (RET, EGFR, VEGFR) and signalling pathways in archival tumor specimens when available.

Condition	Intervention	Phase
Neuroblastoma	Drug: ZD6474 Drug: Retinoic Acid	Phase I

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Safety/Efficacy Study
Official Title:	A Phase I Study of ZD6474 (Zactima) Alone and in Combination With Retinoic Acid in Relapsed and Refractory Pediatric Neuroblastoma

Resource links provided by NLM:

MedlinePlus related topics: Cancer Neuroblastoma

Drug Information available for: Vandetanib Tretinoin Isotretinoin

U.S. FDA Resources

Further study details as provided by M.D. Anderson Cancer Center:

Primary Outcome Measures:

Maximum tolerated dose (MTD) [ Time Frame: 28 day cycles, first 2 cycles used to determine dose-limiting toxicity ] [ Designated as safety issue: Yes ]

Estimated Enrollment:	84
Study Start Date:	September 2007
Estimated Primary Completion Date:	September 2014 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
1: Experimental Part A = ZD6474 Alone; Part B, C = ZD6474 + Retinoic Acid	Drug: ZD6474 Part A = Starting dose 50 mg/m^2 by mouth daily for 28 days; Part B, C = Starting dose 50 mg/m^2 by mouth daily on days 2-28. Drug: Retinoic Acid Part B, C = 80 mg/m^2 by mouth twice daily for 2 consecutive weeks out of every four weeks (28 days).

Hide Detailed Description

Detailed Description:

The Study Drugs:

ZD6474 is a drug that slows down the function of proteins in tumor cells called protein tyrosine kinases. Tyrosine kinases normally cause tumor cells to grow. It is thought to have anti-cancer effects when given with or without other chemotherapy drugs.

Isotretinoin has been shown to help stop the growth of neuroblastoma cells. It helps cells look more normal and grow more slowly.

Screening Tests:

Before you can receive the study drugs, you will have what are called "screening tests." These tests will help the doctor decide if you are eligible to take part in the study.

Your complete medical history will be recorded.
You will have a physical exam.
Blood (about 2 teaspoons) and urine will be collected for routine tests. This routine blood draw will include a pregnancy test for women who are able to have children. To be eligible to take part in this study, the pregnancy test must be negative.
You will have an echocardiogram (ECHO -- test that uses sound waves to create a moving picture of the heart).
You will have an electrocardiogram (ECG -- test that records the electrical activity of the heart).
You will have a computed tomography (CT) scan, a magnetic resonance imaging (MRI) scan, or a bone scan to check the status of the disease.
You will have MIBG (iodine-123-meta-iodobenzylguanidine) scans to check the status of the disease. Your doctor will describe this procedure to you in more detail and you will be given a separate consent form to sign.
A special urine test will also be done to check the levels of homovanillic acid (HVA) and vanillylmandelic acid (VMA), chemicals produced by most neuroblastoma tumors. You will be told how to prepare for the test.

Study Drug Dose Level and Drug Administration:

There will be 3 parts in the study. In Part A, participants will receive the study drug ZD6474 alone. In the Part B portion, participants will receive ZD6474 along with isotretinoin. In Part C, an additional number of participants will be enrolled and will receive ZD6474 along with isotretinoin at the highest dose level that was found in Part B.

Participants in Part A will take ZD6474 daily by mouth in the form of pills or liquid for 28 days. This 28-day period is called a study "cycle." In Part A, the study drug will be given at different doses. Three (3) participants will be enrolled in each dose level. New groups will continue to be enrolled at higher doses until intolerable side effects are seen. If you are assigned to Part A, the dose assigned to you will depend on the number of participants that have been enrolled before you and the side effects they may have experienced.

Once the highest tolerable dose of ZD6474 is found, participants will then begin enrolling in Part B.

Participants in Part B Cycle 1 only will take ZD6474 daily by mouth in the form of pills or liquid on Days 2-28 on each 28-day cycle. Participants will also take isotretinoin by mouth 2 times a day every day for 2 weeks in a row, at some point during the 28-day cycle.

In Part C, participants will follow the same schedule as in Part B.

You will be given a "diary" to record when you take the study drugs. You will need to bring the diary with you to each study visit. At each visit, you will also be asked about any side effects that you may be experiencing.

Study Visits:

During the first 2 months of the study, you will have a study visit weekly. After the first 2 months, you will have study visits at least 1 time a month. At these visits, the following tests and procedures will be performed.

Your complete medical history will be recorded.
You will have a physical exam.
Blood (about 2 teaspoons) and urine will be collected for routine tests. Once a month, this routine blood/urine test will include a pregnancy test for women who are able to have children.
You will be asked about any drugs you may be taking and if you have been able to maintain a healthy diet.

Every week for the first month, every other week for Month 2, and then once a month after that, you will have ECGs to make sure that your heart remains healthy.

Pharmacokinetic Testing:

Extra blood samples will be drawn during the study for pharmacokinetic (PK) test. PK tests are used to measure the amount of study drug in the blood. The amount of blood draw will be less than 1 teaspoon each time.

Blood will be drawn for PK testing at the following time points:
On Day 1 of Cycle 1, before and 6 hours after taking ZD6474
On Days 2, 8, 15 and 22 of Cycle 1 before you take ZD6474
On Days 1, 8 and 15 of Cycle 2 before you take ZD6474
On Day 1 of Cycles 4, 6, and 8 before taking ZD6474

If you are 1 of the first 3 participants enrolled in the study, blood will be drawn at 2, 4, 6, and 8 or 12 and 24 hours after the very first dose during Cycle 1.

Length of Study:

You may remain on study for as long as you are benefitting. You will be taken off study early if the disease gets worse or intolerable side effects occur.

End-Of-Study Visit:

Once you are off study, you will have an end-of-study visit. At this visit, the following tests and procedures will be performed. If any tests or procedure has been performed in the last month, it will not be repeated.

Your complete medical history will be recorded.
You will have a physical exam.
Blood (about 2 teaspoons) and urine will be collected for routine tests. This routine blood draw will include a pregnancy test for women who are able to have children.
You will have an ECHO.
You will have an ECG.
You will have a CT scan, MRI scan, or a bone scan to check the status of the disease.
You will have MIBG scans to check the status of the disease.
A special urine test will also be done to check the levels of HVA and VMA.

Follow-up Visits:

You will have follow-up visits every month once you are off study. These visits will continue indefinitely. At these visits, you will have the following tests and procedures performed.
Your complete medical history will be recorded.
You will have a physical exam.
Blood (about 2 teaspoons) and urine will be collected for routine tests.

Additional Information:

Tell your doctor right away if you have rash, diarrhea, vomiting, changes in the heart rhythm (such as fast or irregular heart beating), high fever, fainting or dizzy spells, light-headedness, chest discomfort, shortness of breath, or are unable to eat normally.
Avoiding direct sunlight.
Cover sun-exposed skin with clothing (long pants, long sleeve shirts, and hats).

Use an SPF 45 or higher sunblock.

This is an investigational study. ZD6474 is FDA approved for the treatment of follicular, medullary, anaplastic, and locally advanced and metastatic papillary thyroid cancer. Isotretinoin is FDA approved for acne. The use of these drugs for this disease and the use of the drugs together is investigational. Up to 84 patients will take part in this study. All will be enrolled at M. D. Anderson.

Eligibility

Ages Eligible for Study:	2 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Provision of informed consent from subjects or their legal guardians
Patients must have had histologic verification of neuroblastoma and/or demonstration of tumor cells in the bone marrow with increased urinary catecholamines (HVA and/or VMA) at the time of initial diagnosis, AND which has progressed on standard therapy, relapsed after standard therapy, or for which no standard curative therapy is known.
Measurable or evaluable disease presence within 4 weeks of onset of study therapy: a. measurable tumor on MRI, CT scan or X-ray obtained prior to study entry. Patients who appear to have residual stable tumor upon completion of frontline therapy must undergo a biopsy to document presence of viable neuroblastoma. If only active target lesion was radiated of patients with stable disease, biopsy must be done at least 4 weeks after radiation was completed and must demonstrate viable neuroblastoma, OR
(Continued # 3): Evaluable disease documented by bone marrow obtained prior to study entry with tumor cells seen on routine morphology (not by NSE staining only) of aspirate and/or biopsy OR
(Continued # 3) Evaluable disease documented by MIBG scan or bone scan obtained within 4 weeks prior to study entry with positive uptake at a minimum of one site. Patients who appear to have residual stable MIBG positive lesions upon completion of frontline therapy must undergo a biopsy to document the presence of viable neuroblastoma. If the patient has only one MIBG positive lesion and that lesion was radiated, a biopsy must be done at least 4 weeks after radiation was completed and must demonstrate viable neuroblastoma.
Performance status - Lansky play or karnofsky score of >40
Age >/=2 years at time of enrollment

Exclusion Criteria:

Lab results: a) ANC <1000/mm^3, hemoglobin <7.0 g/dL, platelets <20,000/mm^3 (hemoglobin and platelets may be supported by transfusions); b) Serum bilirubin >1.5x institutional upper limit of normal (IULN); c) Serum creatinine >1.5 x per IULN or creatinine clearance <or equal to 70 ml/min/1.73m^2; d) Potassium, <4.0 mmol/L despite supplement; Serum calcium or ionized calcium >IULN; Magnesium out of normal range per institutional guidelines despite supplement; e) ALT > 2.5 X IULN or alkaline phosphatase (ALP) >2.5 X IULN or > 5X IULN if judged by the investigator to be related to liver metastases
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 trial or which would jeopardize compliance with the protocol.
History of symptomatic or medically managed arrhythmia (multifocal premature ventricular contractions (PVCs), bigeminy, trigeminy, ventricular tachycardia, or uncontrolled atrial fibrillation) (>/= NCI CTCAE grade 3) or asymptomatic sustained ventricular tachycardia. Atrial fibrillation controlled on medication is not excluded.
Previous history of QTc prolongation as a result from other medication that required discontinuation of that medication.
Congenital long QT syndrome, or 1st 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. If a patient has QTc >/=480 msec on screening ECG, the screen ECG may be repeated twice (at least 24 hours apart). The average QTc from the three screening ECGs must be <480 msec in order for the patient to be eligible for the study.
Use of any concomitant medication that may cause QTc prolongation, induce Torsades de Pointes or induce CYP3A4 function
Clinically significant cardiac event such as myocardial infarction, TIA, or CVA within 3 months before entry; or presence of cardiac disease that, in the opinion of the Investigator, increases the risk of ventricular arrhythmia.
Hypertension > 95th percentile for age (either systolic or diastolic) or > 140/90 for patients >18 years of age and uncontrolled by oral medication at onset of study therapy.
Currently active diarrhea that may affect the ability of the patient to absorb the ZACTIMA.
Women who are currently pregnant or breastfeeding.
Receipt of any investigational agents within 14 days prior to commencing study treatment, or prior receipt of ZACTIMA at any time
Last dose of prior chemotherapy discontinued less than 2 weeks before the start of study therapy.
Last radiation therapy within the last 4 weeks before the start of study therapy, except palliative radiotherapy to non-index lesions
Any unresolved non-hematologic toxicity greater than CTC grade 1 from previous anti-cancer therapy, except for platinum-induced hearing loss.
Any evidence of active graft versus host disease after stem cell transplant.
Major surgery within 4 weeks, or incompletely healed surgical incision before starting study therapy.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00533169

Contacts

Contact: Peter E. Zage, MD, PhD

713-792-6624

Locations

United States, Texas
U.T.M.D. Anderson Cancer Center	Recruiting
Houston, Texas, United States, 77030
Principal Investigator: Peter E. Zage, MD, PhD

Sponsors and Collaborators

M.D. Anderson Cancer Center

AstraZeneca

Investigators

Principal Investigator:

Peter E. Zage, MD, PhD

U.T.M.D. Anderson Cancer Center

More Information

Additional Information:

MD Anderson Cancer Center website This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	U.T.M.D. Anderson Cancer Center ( Peter E. Zage, MD, PhD/Assistant Professor )
Study ID Numbers:	2006-0807
Study First Received:	September 19, 2007
Last Updated:	October 16, 2009
ClinicalTrials.gov Identifier:	NCT00533169 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by M.D. Anderson Cancer Center:

Neuroblastoma
ZD6474
Zactima
Isotretinoin

13-Cis Retinoic Acid
Accutane
Pediatric Neuroblastoma

Additional relevant MeSH terms:

Neuroectodermal Tumors, Primitive
Neoplasms by Histologic Type
Antineoplastic Agents
Neoplasms, Nerve Tissue
Pharmacologic Actions
Neuroblastoma
Keratolytic Agents
Neuroectodermal Tumors
Neoplasms

Therapeutic Uses
Neoplasms, Germ Cell and Embryonal
Isotretinoin
Tretinoin
Neoplasms, Neuroepithelial
Dermatologic Agents
Neuroectodermal Tumors, Primitive, Peripheral
Neoplasms, Glandular and Epithelial

ClinicalTrials.gov processed this record on November 25, 2009