Selumetinib and Cixutumumab in Treating Patients With Advanced Solid Malignancies

Phase 1

Completed

• Conditions: Adult Solid Neoplasm
• Interventions: Biological: Cixutumumab; Other: Laboratory Biomarker Analysis; Other: Pharmacological Study; Drug: Selumetinib

• Registration Number: NCT01061749
• Lead Sponsor: National Cancer Institute (NCI)

Brief Summary

This phase I clinical trial studies the safety and best dose of selumetinib and cixutumumab in treating patients with advanced solid malignancies. Selumetinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as cixutumumab, can block tumor growth in different ways. Some block the ability of tumor to grow and spread. Others find tumor cells and help kill them or carry \[cancer/tumor\]-killing substances to them.

Detailed Description

PRIMARY OBJECTIVES:

I. Determine the safety and toxicity of the combination of AZD6244 and IMC-A12 in advanced solid tumors that have progressed on standard therapy.

II. Finding the maximum tolerated dose (MTD)/recommended phase II dose of the combination.

SECONDARY OBJECTIVES:

I. Explore preliminary evidence of efficacy of the combination of AZD6244 and IMC-A12 in advanced solid tumors using RECIST criteria for tumor response.

II. Define pharmacodynamic (PD) profile of the combination of IMC-A12 and AZD6244.

III. Correlate pharmacokinetics (PK) of the combination of IMC-A12 and AZD6244 to pharmacodynamic (PD) endpoints.

IV. Assess the PK/PD (phospho-S6) link with AZD6244 when administered in combination with IMC-A12.

OUTLINE: This is a dose-escalation study of selumetinib and cixutumumab.

Patients receive selumetinib orally (PO) twice daily (BID) on days 1-28 and cixutumumab intravenously (IV) on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 4 weeks.

Study Timeline

• Study Start: 2009-11
• Study First Submitted: 2010-02-02
• Study First Submitted QC: 2010-02-02
• Study First Posted: 2010-02-03
• Primary Completion: 2013-04
• Study Completion: 2014-09
• Status Verified: 2014-12
• Last Update Submitted: 2016-01-22
• Last Update Posted: 2016-01-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Patients must have a histologically-confirmed metastatic or locally advanced solid tumor that has failed to respond to standard therapy, progressed despite standard therapy, or for which standard therapy does not exist
• There is no limit on the number of prior treatment regimens
• Patients must be off prior chemotherapy, radiation therapy, hormonal therapy, or biological therapy for at least 4 weeks; patients who were receiving mitomycin C, nitrosoureas, or carboplatin must be 6 weeks from the last administration of chemotherapy; patients with prostate cancer may continue to receive LHRH agonist (unless orchiectomy has been performed)
• ECOG performance status 0-1
• Life expectancy of greater than 3 months
• Leukocytes >= 3,000/mcL
• Absolute neutrophil count >= 1,200/mcL
• Platelets >= 100,000/mcL
• Hemoglobin >= 9 mg/dL
• Albumin >= 2.5 g/dL
• Total bilirubin =< 1.5 X institutional upper limits of normal in the absence of Gilbert's syndrome
• AST(SGOT) and ALT(SGPT) =< 2.5 X institutional upper limit of normal
• Serum glucose =< 120 mg/dL
• Creatinine =< 1.5 mg/dL OR creatinine clearance >= 45 mL/min for patients with creatinine levels above institutional normal.
• Patients must have recovered from toxicity related to prior therapy to at least grade 1 (defined by CTEP Active Version of the CTCAE); chronic stable grade 2 peripheral neuropathy secondary to neurotoxicity from prior therapies may be considered on a case by case basis by the Principal Investigator
• As the effect of AZD6244 and IMC-A12 in combination on the developing human fetus is not known, women of child-bearing potential and men must agree to use adequate contraception (abstinence; hormonal or barrier method of birth control) for the study and at least 3 months after completion
• Female patient of childbearing potential has a negative serum pregnancy test within 7 days of study enrollment
• Ability to understand and the willingness to sign a written informed consent document
• Measurable disease
• Patient must be able to swallow pills
• Patients must have LVEF > 45% before starting therapy as measured by echocardiogram or MUGA
• Patients should have a baseline ophthalmologic examination before starting therapy

Exclusion Criteria

• Patient current evidence of active and uncontrolled infection, documented Child's class B-C cirrhosis, or active pancreatitis

• Uncontrolled hypertension (BP > 150/95 despite optimal therapy)

• Left ventricular ejection fraction of =< 45% or NYHA Class II-IV CHF

• Prior or current cardiomyopathy

• Atrial fibrillation with heart rate > 100 bpm

• Unstable ischemic heart disease (myocardial infarction within 6 months prior to starting treatment, or angina requiring use of nitrates more than once weekly)

• Patients receiving any medications that are inhibitors or inducers of specific CYP450 enzyme(s) are ineligible

• History of growth hormone deficiency or excess, or patient is concurrently using growth hormone (GH), or growth hormone inhibitors

• Patient has a known hypersensitivity to the components of study drugs, its analogs, or drugs of similar chemical or biologic composition

• Patient has prior exposure to IGF-1R or RAF/MEK inhibitors

• The patient has poorly controlled diabetes mellitus, defined as a Hba1c > 7%

• Patients with active CNS metastases and/or carcinomatous meningitis are excluded; however, patients with CNS metastases who have completed a course of therapy would be eligible for the study provided they are clinically stable for 3 months prior to entry as defined as:

  • No evidence of new or enlarging CNS metastasis
  • No new signs or symptoms consistent with CNS metastasis
  • Off steroids or on a stable dose of steroids for at least four weeks

• Patient with a primary central nervous system tumor

• Patient has known psychiatric or substance abuse disorders that is uncontrolled and would interfere with cooperation with the requirements of the trial

• Patient is pregnant or breastfeeding.

• Patient is Human Immunodeficiency virus (HIV)-positive and on highly active antiretroviral therapy (HAART), as drug interactions between those agents and these experimental agents are wholly unknown; if this combination goes forward, this regimen will need to be tested in this group of patients in the future; patients with HIV who are well compensated and do not require HAART therapy are eligible for the study

• Patient has active hepatitis B or C on treatment

• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days of day 1 of therapy

• Use of any other concurrent investigational agents or anticancer agents including hormonal therapy, except in the case of prostate cancer patients who are being treated with LHRH agonist at the time of trial entry

• Patients should avoid excessive sun exposure and use adequate sunscreen protection if sun exposure is anticipated

• History of any serious intraocular or retinal pathology as determined by the reference ophthalmologist, with the exception of controlled glaucoma or cataracts; in particular, patients with a history of retinal vein occlusion (RVC) or central serous retinopathy (CSR), or predisposing factors to RVO or CSR as assessed by ophthalmic exam (e.g. evidence of new optic disc cupping, new visual field defects, intraocular pressure > 21 mmHg, uncontrolled glaucoma or ocular hypertension, uncontrolled systemic disease such as hypertension, diabetes mellitus, or history of hyperviscosity or hypercoagulability syndromes) must be excluded

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Treatment (selumetinib, cixutumumab)	Cixutumumab	Patients receive selumetinib PO BID on days 1-28 and cixutumumab IV on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Treatment (selumetinib, cixutumumab)	Laboratory Biomarker Analysis	Patients receive selumetinib PO BID on days 1-28 and cixutumumab IV on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Treatment (selumetinib, cixutumumab)	Pharmacological Study	Patients receive selumetinib PO BID on days 1-28 and cixutumumab IV on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Treatment (selumetinib, cixutumumab)	Selumetinib	Patients receive selumetinib PO BID on days 1-28 and cixutumumab IV on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Primary Outcome Measures

Name	Time	Method
Maximum tolerated dose of selumetinib in combination with cixutumumab defined as the dose produced DLT in =< 1 out of 6 patients	Up to 4 weeks	The proportion of patients with serious or life threatening toxicities will be estimated along with 95% confidence intervals. Tabulated by dose combination, by toxicity type, and by the severity.

Secondary Outcome Measures

Name	Time	Method
Pharmacokinetics of the combination of selumetinib and cixutumumab	Prior to the dose and at 0.5, 1, 1.5, 2, 4, and 8 hours	Peak serum level (Cmax), the trough level (Cmin), and the Area Under the serum concentration time Curve (AUC) will be summarized using descriptive statistics.
The proportion of patients who experience PR, CR, or SD as defined by RECIST criteria	Up to 4 weeks after completion of study treatment

Trial Locations

Locations (1)

Johns Hopkins University/Sidney Kimmel Cancer Center; 🇺🇸 Baltimore, Maryland, United States