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AMP-224, a PD-1 Inhibitor, With Stereotactic Body Radiation Therapy in Metastatic Colorectal Cancer

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ClinicalTrials.gov Identifier: NCT02298946
Recruitment Status : Completed
First Posted : November 24, 2014
Results First Posted : February 22, 2019
Last Update Posted : February 22, 2019
Sponsor:
Information provided by (Responsible Party):
Tim Greten, M.D., National Cancer Institute (NCI)

Brief Summary:

Background:

- T-cells are white blood cells that can find and kill germs and tumors. Cancer can keep T-cells from working. Researchers think a new drug called AMP-224 might help the T-cells in people with cancer. They think the drug might work even better when combined with a certain type of radiation therapy.

Objective:

- To study the safety and effectiveness of AMP-224 together with 1 or 3 days of stereotactic body radiation therapy (SBRT) directed to the liver.

Eligibility:

- People age 18 and older with metastatic colorectal cancer. Their cancer must have spread to the liver and not be responding to treatment.

Design:

  • Participants will be screened with a medical history, physical exam, and blood and urine tests. Their tumors will be measured with computerized tomography (CT) scans or magnetic resonance imaging (MRI) of the chest, stomach, and pelvis. They will have an electrocardiogram (ECG) heart test.
  • Participants will have a small part of their tumor removed by needle (biopsy).
  • Participants will have 8 study visits over about 10 weeks.
  • At 1 visit, they will have another tumor biopsy.
  • At 1 visit, they will get a chemotherapy drug through a vein (intravenous (IV)).
  • At 6 visits, they will receive AMP-224 through an IV.
  • At 1 or 3 visits, they will have SBRT. Computed tomography (CT) scans will map the position of their tumor. Radiation beams of different intensities at different angles will be directed to the tumor.
  • At all visits, some screening procedures may be repeated.
  • After treatment ends, participants will have 7 follow-up visits over about 5 months. Blood will be drawn. Some screening procedures may be repeated.

Condition or disease Intervention/treatment Phase
Colorectal Cancer Colorectal Neoplasms Colorectal Carcinoma Drug: AMP-224 Radiation: Stereotactic Body Radiation Therapy(SBRT) Drug: Cyclophosphamide Phase 1

  Show Detailed Description

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 17 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Pilot Study of AMP-224, a PD-1 Inhibitor, in Combination With Stereotactic Body Radiation Therapy (SBRT) in Patients With Metastatic Colorectal Cancer
Actual Study Start Date : November 21, 2014
Actual Primary Completion Date : July 13, 2016
Actual Study Completion Date : March 7, 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: DL1 - CTX, SBRTx1 day, & AMP-224
Dose Level 1 (DL1) Cyclophosphamide (CTX) 200mg/m(2) intravenous (IV) on day 0. Stereotactic body radiation therapy (SBRT) 8 (gray)Gy x 1 day on day 0, AMP-224 10mg/kg on day 1 then every (q)14 days for a total of 6 doses
Drug: AMP-224
10mg/kg on day 1 then every 14 days for a total of 6 doses.

Radiation: Stereotactic Body Radiation Therapy(SBRT)
Dose Level 1: 8Gy x 1 day. Dose Level 2: 8Gy x 3 days

Drug: Cyclophosphamide
200mg/m(2) IV on day 0.
Other Name: CTX

Experimental: DL2 - CTX, SBRTx3 days, and AMP-224
Dose Level 2 (DL2) CTX 200mg/m(2) IV on day 0, SBRT 8Gy x 3 day on days -2, -1, and 0. AMP-224 10mg/kg on day 1 then q14 days.
Drug: AMP-224
10mg/kg on day 1 then every 14 days for a total of 6 doses.

Radiation: Stereotactic Body Radiation Therapy(SBRT)
Dose Level 1: 8Gy x 1 day. Dose Level 2: 8Gy x 3 days

Drug: Cyclophosphamide
200mg/m(2) IV on day 0.
Other Name: CTX




Primary Outcome Measures :
  1. Count of Participants With Serious and Non-serious Adverse Events Assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0) [ Time Frame: Date treatment consent signed to date off study, approximately 24 months and 8 days ]
    Here is the count of participants with serious and non-serious adverse events assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned.


Secondary Outcome Measures :
  1. Duration of Response in Patients With Colorectal Cancer During and Following Treatment With AMP-224 in Combination With SBRT [ Time Frame: 12 months ]
    Duration of overall response is measured from the time measurement criteria are met for complete response (CR) or partial response (PR) (whichever is recorded first) until the first date that recurrent or progressive disease is objectively documented (taking as reference for progressive disease the smallest measurements recorded since the treatment started). Response was assessed by the Response Evaluation Criteria in Solid Tumors (RECIST). Complete response is complete disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Partial response is at least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum of diameters.

  2. Number of Participants in Which Specimens Were Collected for Pre and Post Pharmacokinetic (PK) AMP-224 Analyses [ Time Frame: Baseline and post infusion AMP-224 (e.g. 15 minutes after infusion ended) ]
    This outcome measure only represents the number of participants with metastatic colorectal cancer who had specimens collected for pre and post pharmacokinetic (PK) AMP-224 analyses.

  3. Overall Survival in Patients With Colorectal Cancer Following Treatment With AMP-224 in Combination With SBRT [ Time Frame: Baseline to end of study, which is date of death. Average time participants were followed was 10.6 months. ]
    Overall survival is defined as the time from treatment start date until date of death or date last known alive.

  4. Count of Participants With Post-Treatment Biopsies [ Time Frame: Post treatment, day 29 +/- 7 days ]
    Mandatory post treatment biopsies of the tumor were attempted on all patients.

  5. Median Progression-free Survival in Patients With Colorectal Cancer [ Time Frame: Baseline to disease progression, an average of 2.6 months. ]
    Progression free survival is defined as the time interval from start of treatment to documented evidence of disease progression. Disease progression was evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 and is at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5mm. (Note: the appearance of one or more new lesions is also considered progressions).

  6. Objective Response Rate [ Time Frame: Restaging was done every 8 weeks for an average of 2.6 months. ]
    Objective response will be evaluated according to the revised Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 and is defined as Complete Response + Partial Response. Briefly, complete response (CR) is defined as the disappearance of all target lesions, and Partial Response is defined as "at least" 30% decrease in the sum of the diameters of the target lesions from baseline measurement.

  7. Immunogenicity of AMP-224 as Measured by Human Anti-Murine Antibodies (HAMA) and Human Anti-Chimeric Antibodies (HACA) Concentrations [ Time Frame: Baseline, D1, D29, and D57 (pre-infusion), D79, D85 and 90 days post last dose (D169) ]
    Blood samples were collected to measure HAMA and HACA concentrations using the ELISA method in all patients.

  8. Terminal Elimination Half-Life of AMP-224 [ Time Frame: 10 days ]
    Plasma decay half-life is the time measured for the plasma concentration of the drug to decrease by one half.

  9. Area of the Curve (AUC) of AMP-224 [ Time Frame: Pre and post-infusion with all the AMP infusion and Day 1 at 8, 15, 29, 43, 57, and 71 hours. ]
    The AUC is a measure of the serum concentration of the drug over time. It is used to characterize drug absorption. The lower limit of quantification (LLOQ) is the smallest concentration of the drug that can be reliably measured.

  10. Time to Maximum Observed Plasma Concentration (Tmax) of AMP-224 [ Time Frame: 12.7 hours following intravenous (IV) infusion. ]
    Time maximum drug absorption is reached in the blood following administration of AMP-224.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 99 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

-Inclusion Criteria

  1. Patients must have histopathological confirmation of Colorectal Carcinoma (CRC) by the Laboratory of Pathology of the National Cancer Institute (NCI) prior to entering this study.
  2. Patients must have progressed on or been intolerant of prior oxaliplatin and irinotecan containing chemotherapeutic regimen and have disease that is not amenable to potentially curative resection. Patients who have a known KRAS wild type tumor must have progressed or been intolerant to cetuximab or panitumumab-based chemotherapy.
  3. Patients must have one focus of metastatic disease in the liver that is amenable to stereotactic body radiation therapy (SBRT) in the opinion of radiation oncology.
  4. All patients enrolled will be required to have measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria outside the radiation field.
  5. Study patients must have disease that is amenable to pre and post treatment biopsy and be willing to undergo this.
  6. Age greater than or equal 18 years
  7. Life expectancy of greater than 3 months
  8. Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  9. Patients must have acceptable organ and marrow function as defined below:

    • leukocytes less than or equal to 3,000/mcL
    • absolute neutrophil count less than or equal 1,500/mcL
    • platelets less than or equal 100,000/mcL
    • total bilirubin greater than or equal 1.5X institution upper limit of normal
    • Patients are eligible with alanine aminotransferase (ALT) or aspartate aminotransferase (AST) measuring up to 5 x ULN given the presence of liver metastasis.
    • creatinine greater than 1.5X institution upper limit of normal

    Or

    -creatinine clearance less than or equal 45 mL/min/1.73 m(2), as calculated below, for patients with creatinine levels above institutional normal

  10. Patients must have recovered from any acute toxicity related to prior therapy, including surgery. Toxicity should be less than or equal to grade 1 or returned to baseline.
  11. Patients must not have other invasive malignancies within the past 3 years (with the exception of non-melanoma skin cancers, localized prostate cancer, carcinoma in situ of the cervix and non-invasive bladder cancer that has had successful curative treatment).
  12. Patient must be able to understand and willing to sign a written informed consent document.

Exclusion Criteria

  1. Prior immune checkpoint inhibition with anti-programmed cell death-1 (PD1)/programmed death ligand-1(PD-L1) or anti-cytotoxic T-lymphocyte antigen 4 (CTLA4) therapy or other specific T cell targeting agents.
  2. Patients who have had chemotherapy (or so-called targeted systemic therapy), large field radiotherapy, or major surgery must wait 4 weeks after completing treatment prior to entering the study.
  3. Patients with known brain metastases will be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.
  4. Uncontrolled intercurrent illness including, but not limited to, hypertension (systolic blood pressure (BP) greater than 160, diastolic BP greater than 100), ongoing or active systemic infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled diabetes or psychiatric illness/social situations that would limit compliance with study requirements.
  5. Human immunodeficiency virus (HIV)-positive patients receiving anti-retroviral therapy are excluded from this study due to the possibility of pharmacokinetic interactions between antiretroviral medications and the investigational agent.
  6. History of chronic autoimmune disease (e.g., systemic lupus erythematosus or Wegener's granulomatosis, Addison's disease, multiple sclerosis, Graves disease, Hashimoto's thyroiditis, hypophysitis, etc.) with symptomatic disease within the 3 years before randomization. Note: Active vitiligo or a history of vitiligo will not be a basis for exclusion. In addition, a past history of certain autoimmunity eg rheumatoid arthritis or thyroiditis may be allowed per principal investigator (PI) discretion provided it has been quiescent for a minimum of three years.
  7. Active or history of inflammatory bowel disease (colitis, Crohn's), irritable bowel disease, celiac disease, or other serious, chronic, gastrointestinal conditions associated with diarrhea.
  8. Dementia or significantly altered mental status that would prohibit the understanding or rendering of Information and Consent and compliance with the requirements of the protocol.
  9. Currently receiving immunosuppressive doses of steroids or other immunosuppressive medications (inhaled and topical steroids are permitted)
  10. History of sarcoidosis syndrome
  11. History of hypersensitivity reaction to human or mouse antibody products.
  12. Pregnancy and breast feeding are exclusion factors. The effects of AMP-224 on the developing human fetus are unknown. Enrolled patients must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, the duration of study participation and 3 months after the end of the treatment. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.
  13. Patients with unhealed surgical wounds for more than 30 days.
  14. Patients with known sensitivity or allergy to any components of AMP-224.

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): NCT02298946


Locations
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United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States, 20892
Sponsors and Collaborators
National Cancer Institute (NCI)
Investigators
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Principal Investigator: Tim F Greten, M.D. National Cancer Institute (NCI)
  Study Documents (Full-Text)

Documents provided by Tim Greten, M.D., National Cancer Institute (NCI):
Informed Consent Form  [PDF] August 27, 2016


Additional Information:
Publications:
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Responsible Party: Tim Greten, M.D., Principal Investigator, National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT02298946     History of Changes
Other Study ID Numbers: 150021
15-C-0021
First Posted: November 24, 2014    Key Record Dates
Results First Posted: February 22, 2019
Last Update Posted: February 22, 2019
Last Verified: February 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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

Keywords provided by Tim Greten, M.D., National Cancer Institute (NCI):
Anti-PD1 Therapy
Anti-Tumor Immunity
Liver Metastatic
B7-DC Fc Fusion Protein

Additional relevant MeSH terms:
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Colorectal Neoplasms
Intestinal Neoplasms
Gastrointestinal Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Neoplasms
Digestive System Diseases
Gastrointestinal Diseases
Colonic Diseases
Intestinal Diseases
Rectal Diseases
Cyclophosphamide
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Antirheumatic Agents
Antineoplastic Agents, Alkylating
Alkylating Agents
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Myeloablative Agonists