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EphA2 siRNA in Treating Patients With Advanced or Recurrent Solid Tumors

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ClinicalTrials.gov Identifier: NCT01591356
Recruitment Status : Recruiting
First Posted : May 4, 2012
Last Update Posted : May 29, 2019
Sponsor:
Collaborator:
National Cancer Institute (NCI)
Information provided by (Responsible Party):
M.D. Anderson Cancer Center

Brief Summary:
This phase I trial studies the side effects and best dose of EphA2 siRNA (ephrin type-A receptor 2 [EphA2]-targeting 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine [DOPC]-encapsulated short-interfering ribonucleic acid [siRNA]) in treating patients with solid tumors that have spread to other places in the body and usually cannot be cured or controlled with treatment (advanced) or have come back after a period of improvement (recurrent). EphA2-targeting DOPC-encapsulated siRNA may slow the growth of tumor cells by shutting down the activity of a gene that causes tumor growth.

Condition or disease Intervention/treatment Phase
Advanced Malignant Solid Neoplasm Drug: EphA2-targeting DOPC-encapsulated siRNA Other: Laboratory Biomarker Analysis Other: Pharmacological Study Phase 1

Detailed Description:

PRIMARY OBJECTIVES:

I. To determine the safety and tolerability (toxicity profile) of EphA2 siRNA delivered via neutral liposome (1,2-dioleoyl-sn-glycero-3-phosphatidylcholine or DOPC) administered intravenously in patients with advanced/recurrent malignancies.

II. To determine the maximal tolerated dose (MTD) or maximal administered dose (MAD) using a modified toxicity probability interval (mTPI) design.

SECONDARY OBJECTIVES:

I. To determine efficacy (EphA2 expression modulation) at the MTD or MAD. II. To evaluate the effect of EphA2 siRNA-DOPC on tumor and endothelial cell apoptosis.

III. To record the clinical activity (objective response, duration of response, and time to treatment progression) of intravenous (IV) EphA2 siRNA -DOPC.

EXPLORATORY OBJECTIVES:

I. To determine the pharmacokinetic profile of siRNA-EphA2-DOPC in blood. II. To determine the effect of EphA2 siRNA-DOPC on tumor perfusion, apparent diffusion, and metabolism by radiographic imaging (dynamic contrast-enhanced-magnetic resonance imaging [DCE-MRI], diffusion weighted [DW]-MRI and fludeoxyglucose F-18-positron emission tomography [18FDG-PET]).

III. To determine the impact of EphA2 siRNA-DOPC on surrogate biomarkers in blood (cell-free deoxyribonucleic acid [DNA], plasma/serum markers [vascular endothelial growth factor (VEGF), caveolin 1 (CAV1), soluble EphrinA1], and exosomes).

OUTLINE: This is a dose-escalation study.

Patients receive EphA2-targeting DOPC-encapsulated siRNA IV over 120 minutes on days 1 and 4. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up periodically.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: EphA2 Gene Targeting Using Neutral Liposomal Small Interfering RNA Delivery: A Phase I Clinical Trial
Actual Study Start Date : July 1, 2015
Estimated Primary Completion Date : July 31, 2020
Estimated Study Completion Date : July 31, 2020

Arm Intervention/treatment
Experimental: Treatment (EphA2-targeting DOPC-encapsulated siRNA)
Patients receive EphA2-targeting DOPC-encapsulated siRNA IV over 120 minutes on days 1 and 4. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
Drug: EphA2-targeting DOPC-encapsulated siRNA
Given IV
Other Name: siRNA-EphA2-DOPC

Other: Laboratory Biomarker Analysis
Correlative studies

Other: Pharmacological Study
Correlative studies




Primary Outcome Measures :
  1. Determine the number of DLTs in patients receiving their first cycle of ephrin type-A receptor 2-targeting 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine-encapsulated short-interfering ribonucleic acid [ Time Frame: Up to 5 years ]
    Will be graded according to Common Terminology Criteria for Adverse Events version 4.0

  2. Maximal tolerated dose or maximal administered dose [ Time Frame: Up to 21 days ]
    Will be defined as the dose level with the smallest difference among all tried doses. Will be determined using modified toxicity probability interval design.


Secondary Outcome Measures :
  1. Percent of patients with ephrin type-A receptor 2 expression modulation, defined as a 50% decrease from baseline expression [ Time Frame: Up to 5 years ]
    Will be calculated along with 90% exact confidence intervals.

  2. Changes in ephrin type-A receptor 2 expression [ Time Frame: Baseline to up to day 4 of course 1 ]
    Tissue effects will be assessed in core biopsy samples collected pre-treatment and course 1 day 2 or day 3 (timed with biomarker assessment).

  3. Changes in endothelial and tumor cell apoptosis conducted by terminal deoxynucleotidyl transferase dUTP nick end labeling assay [ Time Frame: Up to 5 years ]
    Analysis will be performed for both between (dose-effect) and within (changes from baseline) patient cohorts.

  4. Objective response [ Time Frame: Up to 5 years ]
  5. Duration of response [ Time Frame: Up to 5 years ]
  6. Time to treatment progression [ Time Frame: Up to 5 years ]

Other Outcome Measures:
  1. To determine the effect of EphA2 siRNA-DOPC on tumor perfusion by Dynamic Contrast Enhanced-MRI [ Time Frame: [Time Frame: Pre-treatment (within 14 days of Cycle 1 Day 1), Cycle 1 Day 3 or 4 (timed with the tissue core biopsy), and at the end of Cycle 1 (Cycle 1 Day 21± 2 days) prior to Cycle 2.] ]
  2. Pharmacokinetic parameters [ Time Frame: Baseline,15 minutes from start of infusion, 2, 15, 30, 60, 90, 180, 360 minutes, and 24 hours following the end of infusion on day 1 of course 1 and pre-treatment and at the end of second infusion on day 4 of course 1 ]
  3. Circulating biomarkers [ Time Frame: Up to 5 years ]
    Blood will be collected for evaluation of cell-free deoxyribonucleic acid, and plasma/serum markers (vascular endothelial growth factor, caveolin 1, soluble EphrinA1) and exosomes will be evaluated to determine within-patient effects at early (after first infusion on cycle 1 day 4) and late (cycle 3 day 1 pre-dose). Plasma/serum markers will also be evaluated at the end of dosing timepoint. Correlative analysis will be made both between and within patient cohorts.

  4. To determine the effect of EphA2 siRNA-DOPC on apparent diffusion by Diffusion-weighted imaging [ Time Frame: [Time Frame: Pre-treatment (within 14 days of Cycle 1 Day 1), Cycle 1 Day 3 or 4 (timed with the tissue core biopsy), and at the end of Cycle 1 (Cycle 1 Day 21± 2 days) prior to Cycle 2.] ]
  5. To determine the effect of EphA2 siRNA-DOPC on metabolism by FDG-PET [ Time Frame: [Time Frame: Pre-treatment (within 14 days of Cycle 1 Day 1), Cycle 1 Day 3 or 4 (timed with the tissue core biopsy), and at the end of Cycle 1 (Cycle 1 Day 21± 2 days) prior to Cycle 2.] ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All patients with histologic proof of advanced solid tumors, who are not candidates for known regimens or protocol treatments of higher efficacy or priority
  • Eastern Cooperative Oncology Group (ECOG) performance status =< 2
  • All patients (dose escalation and dose expansion phases) must be willing to undergo pre- and post-treatment biopsies
  • For the dose escalation phase, the trial population will be limited to solid tumor types
  • For dose expansion phase: patients must have EphA2 overexpression overall H-score of 3 or above in immunohistochemistry (IHC) evaluation; Clinical Laboratory Improvement Amendments (CLIA) certified EphA2 IHC staining to be performed on formalin fixed, paraffin-embedded tissue sections using monoclonal EphA2 antibody; EphA2 expression to be assessed through a combo of % of positive cells and staining intensity; the % of positive cells will be rated: 0 points (pts), 0 to 5%; 2 pts, 6 to 50%; 3 pts, 50%; the staining intensity will be rated as follows: 1 pt, weak intensity; 2 pts, moderate intensity; 3 pts, strong intensity; pts for expression and % of positive cells will be added; an overall score will be assigned; tumors to be categorized into 4 groups: negative (overall score 0), 5% cells stained, regardless of intensity; weak expression (overall score 1), 1 - 2 pts; moderate expression (overall score 2), 3 - 4 pts; and strong expression (overall score 3), 5 - 6 pts; overall H-score of 3 or above will be defined as EphA2 overexpression in tumor cells
  • Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension; at least one biopsiable lesion must be available; when imaging (DCE-MRI, DW-MRI and PET-computed tomography [CT] imaging) is being performed for secondary objectives (dose level III [or when the dose reaches at least 1,500 ug/m^2] and during the expansion phase) at least one lesion (>= 2 cm) not adjacent to the diaphragm will be required when measured by conventional techniques, including palpation, plain x-ray, CT, and MRI; a second lesion accessible for biopsy must also be present; patients must have at least one 'target lesion' to be used to assess response on this protocol as defined by Response Evaluation Criteria in Solid Tumors (RECIST); this may be one of the lesions mentioned above; tumors within a previously irradiated field will be designated as 'non-target' lesions
  • Resolution of any effects of prior therapy (except alopecia) to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 grade =< 1 and to baseline laboratory values as defined below
  • Hemoglobin (HGB) >= 9 g/dL
  • White blood cells (WBC) >= 3,000/mcL
  • Absolute neutrophil count (ANC) >= 1,500/mcL
  • Platelet (PLT) >= 100,000/mcL
  • Total bilirubin less than or equal to 1.5
  • Serum glutamic oxaloacetic transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT) < 2.5 x institutional upper limit of normal (ULN)
  • Creatinine < 1.5 x ULN or creatinine clearance > 60 ml/min according to Cockcroft-Gault formula
  • Neuropathy (sensory and motor) =< to CTCAE grade 1
  • Prothrombin time (PT) such that international normalized ratio (INR) is < 1.5 (or an in-range INR, usually between 2 and 3, if a patient is on a stable dose of therapeutic warfarin or low molecular weight heparin) and a partial thromboplastin time (PTT) < 1.2 times control
  • Patients should be free of active infection requiring intravenous antibiotics
  • Any hormonal therapy directed at the malignant tumor must be discontinued at least one week prior to registration (study enrollment); continuation of hormone replacement therapy is permitted; stable regimens of hormonal therapy i.e. for prostate cancer (e.g. leuprolide, a gonadotropin-releasing hormone [GnRH] agonist), ovarian or breast cancer are not exclusionary
  • Any other prior therapy directed at the malignant tumor, including immunologic agents, must be discontinued at least three weeks prior to first dose of study drug (6 weeks for nitrosoureas or mitomycin C)
  • Female subject is either post-menopausal or surgically sterilized or willing to use an acceptable method of birth control (i.e., a hormonal contraceptive, intrauterine device, diaphragm with spermicide, condom with spermicide, or abstinence) for the duration of the study and for at least 3 months after completion of EphA2 siRNA-DOPC therapy
  • Male subject agrees to use an acceptable method of contraception for the duration of the study
  • Patients must voluntarily sign an informed consent indicating that they are aware of the investigational nature of this study in keeping with the policies of the hospital

Exclusion Criteria:

  • Patients may not be receiving any other investigational agents and/or other therapy for their cancer
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to DOPC, Magnevist, or fluorodeoxyglucose (FDG)
  • Patients with active bleeding or pathologic conditions that carry high risk of bleeding, such as a known bleeding disorder, coagulopathy, or tumor involving major vessels
  • Patients with history or evidence upon physical examination of central nervous system (CNS) disease, including primary brain tumor, seizures not controlled with standard medical therapy, any brain metastases
  • Patients with history of cerebrovascular accident (CVA, stroke), transient ischemic attack (TIA) or subarachnoid hemorrhage within 6 months of the first date of treatment on this study
  • Patients with clinically significant cardiovascular disease; this includes: uncontrolled hypertension (greater than 140/90); myocardial infarction or unstable angina within 6 months prior to registration; New York Heart Association (NYHA) grade II or greater congestive heart failure; serious cardiac arrhythmia requiring medication; grade II or greater peripheral vascular disease; patients with clinically significant peripheral artery disease, e.g., those with claudication, within 6 months of first date of treatment on this study
  • Patients whose circumstances do not permit completion of the study or the required follow-up
  • Patients who are pregnant or nursing
  • History of human immunodeficiency virus (HIV) or HIV-positive patients on combination antiretroviral therapy are ineligible
  • Patients whose tumor is not accessible for a core biopsy
  • Exclusion criteria (MRI specific):

    • Patients who are ineligible to undergo an MRI scan for reasons such as claustrophobia or the presence of implanted devices or metallic foreign bodies that are not magnetic resonance (MR) compatible; patients with a known history of allergic reaction to gadolinium contrast agents; patients with a history of a glomerular filtration rate (GFR) of less than 60 or acute renal disease
  • Exclusion criteria (PET specific):

    • Pregnant or nursing women; extreme claustrophobia; weight near or greater than 350 pounds

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01591356


Contacts
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Contact: Robert Coleman, MD 713-745-3357

Locations
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United States, Texas
M D Anderson Cancer Center Recruiting
Houston, Texas, United States, 77030
Contact: Robert L. Coleman    713-745-3357      
Principal Investigator: Robert L. Coleman         
Sponsors and Collaborators
M.D. Anderson Cancer Center
National Cancer Institute (NCI)
Investigators
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Principal Investigator: Robert L Coleman M.D. Anderson Cancer Center

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier: NCT01591356     History of Changes
Other Study ID Numbers: 2011-0216
NCI-2015-00745 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
RP120214
NCI-2012-00755
2011-0216 ( Other Identifier: M D Anderson Cancer Center )
P30CA016672 ( U.S. NIH Grant/Contract )
P50CA093459 ( U.S. NIH Grant/Contract )
First Posted: May 4, 2012    Key Record Dates
Last Update Posted: May 29, 2019
Last Verified: May 2019

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Neoplasms