MK2206 in Treating Patients With Advanced Liver Cancer That Did Not Respond to Previous Therapy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01239355
Recruitment Status : Terminated (Early termination for discouraging results)
First Posted : November 11, 2010
Results First Posted : October 5, 2015
Last Update Posted : October 5, 2015
Information provided by (Responsible Party):
National Cancer Institute (NCI)

November 10, 2010
November 11, 2010
June 10, 2015
October 5, 2015
October 5, 2015
December 2010
February 2013   (Final data collection date for primary outcome measure)
Progression-free Survival [ Time Frame: Until disease progression or death, up to 26 months ]
Estimated using the product-limit method of Kaplan and Meier. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1), as a 20% increase in the sum of the longest diameter of target lesions (the sum must also demonstrate an absolute increase of at least 5 mm), or a measurable increase in a non-target lesion, or the appearance of new lesions.
Progression-free Survival
Complete list of historical versions of study NCT01239355 on Archive Site
  • Objective Response [ Time Frame: Evaluated for response every 2 cycles (8 weeks) with confirmatory evaluation at least 4 weeks following initial documentation of objective response, up to 26 months ]
    Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Objective Response (OR) = CR + PR
  • Overall Survival [ Time Frame: Until death, up to 26 months ]
    Survival will be estimated by the product-limit (Kaplan-Meier) estimator.
  • Objective responses
  • Survival
  • Toxicities
Not Provided
Not Provided
MK2206 in Treating Patients With Advanced Liver Cancer That Did Not Respond to Previous Therapy
A Phase II Study of MK-2206 in Patients With Advanced Hepatocellular Carcinoma Who Have Failed or Are Intolerant of One Prior Line of Anti-angiogenic Therapy
This phase II trial is studying how well MK2206 works in treating patients with advanced liver cancer that did not respond to previous therapy. MK2206 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.


I. Evaluate the median progression-free survival in patients with advanced hepatocellular carcinoma treated with MK-2206 after failure of one prior line of anti-angiogenic therapy.


I. Evaluate the objective response rate (CR + PR). II. Evaluate the median overall survival. III. Evaluate the tolerability and toxicity profile of MK-2206 in this patient population.

IV. Explore, in a preliminary fashion, potential molecular predictors of efficacy.


Patients receive oral Akt inhibitor MK2206 on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 4 weeks and then every 3-6 months thereafter.

Phase 2
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Adult Hepatocellular Carcinoma
  • Advanced Adult Hepatocellular Carcinoma
  • Localized Non-Resectable Adult Liver Carcinoma
  • Recurrent Adult Liver Carcinoma
  • Drug: Akt Inhibitor MK2206
    Given PO
    Other Name: MK2206
  • Other: Laboratory Biomarker Analysis
    Correlative studies
Experimental: Treatment (Akt inhibitor MK2206)
Patients receive oral Akt inhibitor MK2206 on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
  • Drug: Akt Inhibitor MK2206
  • Other: Laboratory Biomarker Analysis
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
February 2013
February 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Unresectable or metastatic HCC for which standard curative measures do not exist

    • The diagnosis of hepatocellular carcinoma should be based on at least one of the following:

      • The presence of one or more liver lesions, measuring >= 2 cm, with characteristic arterial enhancement and venous washout in the setting of liver cirrhosis and/or hepatitis B or C infection
      • The presence of liver lesion(s) with AFP >= 400
      • Tissue confirmation in the absence of either or both of the above
      • Tissue availability is desired and will be sought, but tissue availability is not mandated for accrual to the study
  • Patients must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension, and that has not been the target of local or regional therapy including transarterial chemoembolization, intra-arterial chemotherapy, ethanol, or RFA ablation
  • One prior line of systemic anti-angiogenic therapy is required; this type of therapy includes, but is not restricted to, sorafenib, bevacizumab, sunitinib, or brivanib given as single agents or in combination with other agents
  • No clinically evident ascites (minimal, medically controlled ascites detectable on imaging studies only is allowed)
  • No Child-Pugh C cirrhosis or Child-Pugh B cirrhosis with more than 7 points
  • No fibrolamellar carcinoma or any mixed variants of HCC with dominant fibrolamellar histology
  • Patients with known brain metastases should be excluded from this clinical trial
  • ECOG 0-1
  • Life expectancy of greater than 3 months
  • Leukocytes >= 3,000/mcL
  • Absolute neutrophil count > 1,000 mcL
  • Platelets >= 70,000/mcL
  • Total bilirubin =< 1.5 institutional upper limit of normal
  • AST (SGOT)/ALT (SGPT) < 5 x institutional upper limit of normal
  • Creatinine within normal institutional limits OR creatinine clearance >= 60 mL/min
  • Serum albumin >= 2.8 g/dL
  • Not pregnant or nursing
  • Fertile patients must use two forms of contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation
  • Must agree to collection of correlative blood samples during the study
  • No patients unable to swallow pills or diagnosed with a gastrointestinal disorder that is likely to interfere with the absorption of MK-2206 or with the patient's ability to take regular oral medication
  • Patients with hyperglycemia should be well controlled on oral agents before the patient enters the trial
  • Patients with HgbA1C levels >= 8% or fasting blood glucose >= 150 mg/dL are not eligible for this study
  • Baseline QTcF > 450 msec (male) or QTcF> 470 msec (female) will exclude patients from entry on study
  • Patients with hepatitis B infection, defined by a positive hepatitis B surface antigen test, should be on suppressive anti-viral therapy

    • Only the following anti-viral therapies are allowed while a patient is on study: tenofovir disoproxil fumarate and entecavir
    • Patients with hypothyroidism must be on a stable dose of thyroid replacement and be clinically euthyroid
  • No esophageal or gastric variceal bleeding within the last 6 months

    • Patients with prior history of variceal bleeding must have had an upper endoscopy (EGD) with appropriate treatment of varices within 6 months prior to study entry
  • No uncontrolled intercurrent illness including, but not limited to:

    • Ongoing or active infection
    • Symptomatic congestive heart failure
    • Unstable angina pectoris
    • Cardiac arrhythmia
    • Psychiatric illness/social situations that would limit compliance with study requirements
  • None of the following:

    • Uncontrolled hypertension (systolic BP > 150 or diastolic BP > 100 on two occasions within two weeks of beginning therapy on this protocol)
    • Myocardial infarction within 6 months
    • NYHA class > II
    • Clinically significant bradycardia related to underlying cardiac disease
    • Clinically significant bundle branch block related to underlying cardiac disease
  • No patients with second primary cancer (except adequately treated nonmelanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumors including lymphomas without bone marrow involvement curatively treated with no evidence of disease for ≥ 5 years)

    • The exception to this criterion is prostate cancer treated definitively with surgery and/or radiation with normal PSA and no clinical evidence of residual or recurrent prostate cancer
  • HIV-positive patients on combination antiretroviral therapy are ineligible
  • No history of allergic reactions attributed to compounds of similar chemical orbiologic composition to MK-2206 or other agents used in the study
  • No medications that cause QTc interval prolongation
  • Any number of prior regional therapies with transarterial chemoembolization, intra-arterial chemotherapy, or ablative therapy is allowed

    • No more than 1 prior line of systemic therapy for advanced and/or unresectable disease
  • No patients who have had anti-angiogenic therapy, chemotherapy, radiotherapy or regional therapy (such as transarterial chemoembolization, intra-arterial chemotherapy) within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier

    • Localized radiation for palliation (i.e., bony metastasis, etc.) given for < 3 days is allowed before therapy and is not subject to the 4-week waiting requirement
    • Local ablative therapy such as radiofrequency ablation or cryotherapy must have been completed more than 2 weeks prior to study entry
  • Patients may not be receiving any other investigational or non-investigational agents or therapies directed at treating their hepatocellular carcinoma
  • Patients may not be receiving any other investigational agents for any condition
  • Patients receiving any medications or substances that are inhibitors or inducers of CYP3A4 are ineligible
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
United States
NCI-2011-02549 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
PHII-105 ( Other Identifier: City of Hope Comprehensive Cancer Center )
8752 ( Other Identifier: CTEP )
P30CA033572 ( U.S. NIH Grant/Contract )
N01CM00038 ( U.S. NIH Grant/Contract )
Not Provided
Not Provided
Not Provided
National Cancer Institute (NCI)
National Cancer Institute (NCI)
Not Provided
Principal Investigator: Anthony El-Khoueiry, MD University of Southern California, Norris
National Cancer Institute (NCI)
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP