Vaccine Therapy With or Without Cyclophosphamide in Treating Patients With Recurrent or Refractory Multiple Myeloma - Full Text View

Sponsors and Collaborators:	Mayo Clinic National Cancer Institute (NCI)
Information provided by:	National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:	NCT00450814

Purpose

RATIONALE: Vaccines made from a gene-modified virus may help the body build an effective immune response to kill cancer cells. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving vaccine therapy together with cyclophosphamide may be an effective treatment for multiple myeloma.

PURPOSE: This phase I trial is studying the side effects and best dose of vaccine therapy when given with or without cyclophosphamide in treating patients with recurrent or refractory multiple myeloma.

Condition	Intervention	Phase
Multiple Myeloma and Plasma Cell Neoplasm	Drug: cyclophosphamide Drug: oncolytic measles virus encoding thyroidal sodium iodide symporter Procedure: biopsy Procedure: flow cytometry Procedure: immunologic technique Procedure: laboratory biomarker analysis Procedure: reverse transcriptase-polymerase chain reaction	Phase I

Genetics Home Reference related topics: aceruloplasminemia hemophilia

MedlinePlus related topics: Cancer Measles Multiple Myeloma

Drug Information available for: Cyclophosphamide Iodine Sodium iodide

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment
Official Title:	Phase I Trial of Systemic Administration of Edmonston Strain of Measles Virus, Genetically Engineered to Express NIS, With or Without Cyclophosphamide, in Patients With Recurrent or Refractory Multiple Myeloma

Further study details as provided by National Cancer Institute (NCI):

Primary Outcome Measures:

Toxicity [ Designated as safety issue: Yes ]
Maximum tolerated dose [ Designated as safety issue: Yes ]

Secondary Outcome Measures:

Hematologic response (complete response, very good partial response, minimal response) [ Designated as safety issue: No ]
Viral replication and shedding [ Designated as safety issue: No ]
Biodistribution and kinetics of viral spread and NIS gene expression [ Designated as safety issue: No ]
Tolerability [ Designated as safety issue: Yes ]

Estimated Enrollment:	54
Study Start Date:	May 2007
Estimated Primary Completion Date:	December 2009 (Final data collection date for primary outcome measure)

Detailed Description:

OBJECTIVES:

Primary

Determine the safety and toxicity of Edmonston vaccine strain oncolytic measles virus encoding thyroidal sodium iodide symporter (MV-NIS) when administered with or without cyclophosphamide in patients with relapsed or refractory multiple myeloma.
Determine the maximum tolerated dose of MV-NIS when administered with or without cyclophosphamide in these patients.

Secondary

Determine the time course of viral gene expression and viral elimination, and the biodistribution of virally infected cells at various time points after treatment with these regimens using iodine I 123 gamma camera imaging.
Assess viral replication, viremia, viral shedding in urine and respiratory secretions, and viral persistence after treatment with these regimens.
Monitor humoral responses to MV-NIS in these patients.
Explore the antimyeloma efficacy (i.e., clinical response rate, time to progression, progression-free survival, duration of response) of the virus using standard myeloma response criteria as well as immunoglobulin free light chain measurements.

OUTLINE: This is a dose-escalation study of oncolytic measles virus encoding thyroidal sodium iodide symporter (MV-NIS). Patients are stratified according to receipt of cyclophosphamide during study treatment (yes vs no). Patients are initially accrued to part 1. Once the maximum tolerated dose (MTD) of MV-NIS alone is determined, subsequent patients are accrued to part 2.

Part 1 (MV-NIS alone): Patients receive MV-NIS IV over 30 minutes on day 1. Cohorts of 3-6 patients receive escalating doses of MV-NIS until the MTD is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity.
Part 2 (MV-NIS and cyclophosphamide): Patients receive cyclophosphamide IV over 30 minutes on day -1 and MV-NIS IV over 30 minutes on day 1.

Cohorts of 3-6 patients receive escalating doses of MV-NIS* in combination with cyclophosphamide until the MTD is determined. The MTD of MV-NIS is defined as in part 1.

NOTE: *Starting dose of MV-NIS is the MTD determined in part 1.

Blood and bone marrow samples are obtained for research studies, including flow cytometry, at baseline and at week 6. Serial measurements of viral RNA in mononuclear cells are conducted in samples of blood, saliva, and urine on days 3, 8, and 15 and are tested for viral replication by quantitative reverse transcriptase-polymerase chain reaction. Measles virus-specific immunity is evaluated at baseline and on day 42.

After the completion of study treatment, patients are followed periodically for 1 year.

PROJECTED ACCRUAL: A total of 54 patients will be accrued for this study.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

DISEASE CHARACTERISTICS:

Diagnosis of recurrent or refractory multiple myeloma
- Previously treated with ≥ 2 nonoverlapping chemotherapeutic combinations
  - Thalidomide and corticosteroids are considered chemotherapy
- No known standard therapy that is definitely capable of extending life expectancy exists

PATIENT CHARACTERISTICS:

ECOG performance status 0-2
Life expectancy ≥ 12 weeks
Absolute neutrophil count ≥ 1,000/mm³
Platelet count ≥ 100,000/mm³
Hemoglobin ≥ 8.5 g/dL
Bilirubin ≤ 1.5 times upper limit of normal (ULN)
AST ≤ 2 times ULN
Creatinine < 2 times ULN
INR ≤ 1.4 times ULN
Thyroid-stimulating hormone 0.3-5.0 mlU/L
Free thyroxine 0.8-1.87 ng/dL
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception during and for 4 weeks after completion of study treatment
No uncontrolled infection
No active tuberculosis
No clinically significant cardiac condition or illness, including any of the following:
- New York Heart Association class III-IV congestive heart failure
- Known symptomatic coronary artery disease
- Symptoms of coronary artery disease on systems review
- Cardiac arrhythmia (atrial fibrillation or supraventricular tachycardia)
No active CNS disorder or seizure disorder
No HIV positivity
No allergy to iodine (not including reactions to IV contrast materials)
No exposure to household individuals ≤ 15 months of age or to any household individual with known immunodeficiency

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
No prior allogeneic hematopoietic stem cell transplantation
No prior exposure to heat-inactivated measles virus vaccine
More than 3 weeks since prior and no other concurrent chemotherapy
More than 4 weeks since prior and no other concurrent immunotherapy
More than 4 weeks since prior biologic therapy
No concurrent radiotherapy
No other concurrent ancillary investigational therapy, including drugs, biologicals, or gene therapy, for therapeutic intent or symptomatic control
Concurrent bisphosphonates as maintenance therapy allowed

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00450814

Locations

United States, Minnesota
Mayo Clinic Cancer Center	Recruiting
Rochester, Minnesota, United States, 55905
Contact: Clinical Trials Office - All Mayo Clinic Locations 507-538-7623

Sponsors and Collaborators

Mayo Clinic

National Cancer Institute (NCI)

Investigators

Study Chair:	Angela Dispenzieri, MD	Mayo Clinic
Investigator:	Morie A. Gertz, MD	Mayo Clinic
Investigator:	Philip R. Greipp, MD	Mayo Clinic
Investigator:	Robert A. Kyle, MD	Mayo Clinic
Investigator:	Martha Q. Lacy, MD	Mayo Clinic
Investigator:	John A. Lust, MD, PhD	Mayo Clinic
Investigator:	S. V. Rajkumar, MD	Mayo Clinic
Investigator:	Thomas E. Witzig, MD	Mayo Clinic
Investigator:	Steve Zeldenrust, MD	Mayo Clinic
Investigator:	Shaji K. Kumar, MD	Mayo Clinic
Investigator:	Gregory Wiseman, MD	Mayo Clinic
Investigator:	Suzanne Hayman, MD	Mayo Clinic
Investigator:	Stephen J. Russell, MD, PhD	Mayo Clinic
Investigator:	Raymund Razonable, MD	Mayo Clinic

More Information

Clinical trial summary from the National Cancer Institute's PDQ® database This link exits the ClinicalTrials.gov site

Study ID Numbers:	CDR0000530389, MAYO-MC038C, MAYO-06-005263
Study First Received:	March 20, 2007
Last Updated:	December 31, 2008
ClinicalTrials.gov Identifier:	NCT00450814
Health Authority:	Unspecified

Keywords provided by National Cancer Institute (NCI):

refractory multiple myeloma
stage III multiple myeloma

Study placed in the following topic categories:

Immunoproliferative Disorders
Measles
Blood Protein Disorders
Hematologic Diseases
Blood Coagulation Disorders
Vascular Diseases
Paraproteinemias
Cyclophosphamide
Hemostatic Disorders

Recurrence
Multiple Myeloma
Virus Diseases
Hemorrhagic Disorders
Multiple myeloma
Iodine
Lymphoproliferative Disorders
Neoplasms, Plasma Cell

Additional relevant MeSH terms:

Neoplasms by Histologic Type
Immune System Diseases
Immunologic Factors
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Physiological Effects of Drugs
Immunosuppressive Agents
Pharmacologic Actions

Neoplasms
Therapeutic Uses
Myeloablative Agonists
Cardiovascular Diseases
Antineoplastic Agents, Alkylating
Antirheumatic Agents
Alkylating Agents

ClinicalTrials.gov processed this record on January 14, 2009