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Continuous Infusion of rhIL-15 for Adults With Advanced Cancer

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ClinicalTrials.gov Identifier: NCT01572493
Recruitment Status : Completed
First Posted : April 6, 2012
Last Update Posted : September 25, 2019
Sponsor:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )

Tracking Information
First Submitted Date  ICMJE April 5, 2012
First Posted Date  ICMJE April 6, 2012
Last Update Posted Date September 25, 2019
Study Start Date  ICMJE April 4, 2012
Actual Primary Completion Date June 20, 2018   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: March 10, 2018)
MTD and DLT [ Time Frame: After one cycle ]
Adverse events will be tabulated/reported by type, grade, and frequency.
Original Primary Outcome Measures  ICMJE
 (submitted: April 5, 2012)
Determine the safety, toxicity profile, DLT and MTD of IL-15 in subjects with metastatic cancers.
Change History Complete list of historical versions of study NCT01572493 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: December 13, 2016)
  • Measure response rate [ Time Frame: After completion of treatment ]
  • Measure time to progression [ Time Frame: When patient has progressive disease ]
  • Measure PKs [ Time Frame: After completion of treatemnt ]
Original Secondary Outcome Measures  ICMJE
 (submitted: April 5, 2012)
  • Determine rhIL-15 PKs.
  • Characterize biological effects of rhIL-15 on T cells and NK cells and T-cells subsets.
  • Evaluate potential antitumor activity of rhIL-15.
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Continuous Infusion of rhIL-15 for Adults With Advanced Cancer
Official Title  ICMJE A Phase I Study of a Continuous Intravenous Infusion of Recombinant Human Interleukin IL-15 (rhIL-15) in Adults With Metastatic Cancers
Brief Summary

Background:

- People with cancer can have a weak immune system as a result of the cancer itself, or from prior treatments. . Still, treatments that stimulate the immune system have been shown to be effective against a number of different cancers. Recombinant human interleukin-15 (rhIL-15) is a drug that is designed to boost the immune system. Researchers are interested in seeing if rhIL-15 can strengthen the immune system's response against cancer. The drug will be given through a vein without a break for 10 days (240 hours).

Objectives:

  • To see rhIL-15 given as a continuous infusion over 10 days can be used to treat advanced cancer
  • Identify the side effects associated with this treatment.

Eligibility:

- Individuals at least 18 years of age with advanced cancer for which there are no effective treatments.

Design:

  • Participants screening procedures will include a physical exam and medical history, laboratory (blood) tests and x-rays (Imaging studies) to determine suitability for the protocol. --Appropriate participants with easily accessible tumor deposits may also be asked to have one pretreatment and one post (cycle 1) treatment tumor biopsy. .
  • Eligible participants will be admitted to the hospital for the rhIL-15 treatment and will spend about 12 days in the hospital. .
  • Participants will receive one 10 day infusion each cycle (about every 42 days) for as long as there are no serious side effects and the disease does not progress.
  • Participants will continue treatment as long as imaging studies show that the tumor continues to shrink or for two additional cycles after it has disappeared from the x-rays to make that the cancer is completely gone.
  • Participants who stop treatment for side effects or because their tumor did not shrink or stopped responding to the treatment will continue to have follow-up visits to monitor the outcome of the rhIL-15 treatment until there is evidence their cancer has progress or they begin another treatment.
Detailed Description

BACKGROUND:

  • Interleukin-15 (IL-15) is a stimulatory cytokine with a number of desirable immunotherapeutic features, and clinical trials evaluating recombinant human (rh) IL-15 are underway.
  • In contrast to IL-2, IL-15 treatment does not stimulate activation-induced cell death of Tcells; potentially inhibits immunosuppressive CD4+CD25+ T regulatory cells, contributes to the proliferation, differentiation and activation of CD8+ T-cells and NK-cells and the maintenance of long-term CD8+ memory T-cells.
  • IL-15 is active in a number of syngeneic mouse preclinical tumor models, and vacciniabased constructs expressing IL-15 induced long-lasting, high-avidity cytotoxic CD8+ Tlymphocyte response that appears to be more effective than similar IL-2 expressing vaccines.
  • Pharmacology/toxicology (pharm/tox) experiments in non-human primate (NHP) rhesus macaques and preliminary results from the first-in-human phase I trial examining rhIL-15 given as an IV bolus (IVB) for 12 consecutive days indicate significant stimulation and expansion of NK-cells and CD8+ T-cells.
  • rhIL-15 given as an IVB at 1 mcg/kg dose level appears to be well tolerated despite the presence of some common cytokine-related side effects indicating that 0.1 mcg/kg/day is an appropriate initial dose level for a phase I safety trial of continuous intravenous infusion (CIV) of rhIL-15.
  • Comparison of the pharmacokinetic and immunologic assessments from the IVB phase I trial with the data from both sets of NHP pharm/tox experiments suggest that CIV of rhIL-15 may have greater potential for stimulating an anticancer cellular immune response with a more manageable safety profile.

OBJECTIVES:

Primary Objective:

- Determine the safety, toxicity profile, dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) of rhIL-15 administered as a CIV for 10 consecutive days (240 hours) in subjects with metastatic unresectable cancers for which curative or palliative measures either do not exist or are not associated with a survival advantage.

ELIGIBILITY CRITERIA:

  • Patients greater than or equal to18 years-old, ECOG PS less than or equal to 1, with pathologically confirmed metastatic unresectable cancers for which curative or palliative measures either do not exist or are not associated with a survival advantage.
  • Patients with measurable or evaluable disease, normal organ and bone marrow function.

DESIGN:

  • This is a single-institution, open-label, non-randomized 3 + 3 design phase I dose escalation study.
  • Groups of 3 to 6 subjects will receive CIV rhIL-15 at doses of 0.1, 0.25, 0.5 1, 2, 4, 6 and 8 mcg/kg/day for 10 days provided that DLT has not been observed.
  • After assessments of the 10-day dosing cohorts have been completed, new groups of 3 to 6 subjects will receive CIVrhIL-15 at doses of 3, 4 and 5 mcg/kg/day for 5 days provided that a DLT has not been observed.
  • Patients with evidence of response and the absence of significant toxicities will be eligible for repeat cycles of treatment.
  • Samples for correlative studies will be obtained prior to treatment and at specific times points during and after treatment to assess pharmacokinetics of rhIL-15, the effect of rhIL-15 on immune cell subset populations and pro-inflammatory cytokine levels in the peripheral blood and for the development of neutralizing anti-rhIL-15 antibodies.
Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 1
Study Design  ICMJE Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE
  • Lymphoma
  • Carcinoma
Intervention  ICMJE
  • Biological: rh IL-15 (10 DAYS)
    Continuous infusion of rhIL-15 IV for first 10 days of each cycle
  • Biological: rh IL-15 (5 DAYS)
    Continuous infusion of rhIL-15 for first 5 days of each cycle
Study Arms  ICMJE
  • Experimental: Arm A1 (Dose Escalation, 10-day Dosing)
    MTD determination in subjects with metastatic cancers receiving rhIL-15 IV for 10 consecutive days
    Intervention: Biological: rh IL-15 (10 DAYS)
  • Experimental: Arm A2 (Dose Expansion, 10-day Dosing)
    Clinical activity evaluation in subjects with metastatic cancers receiving rhIL-15 IV for 10 consecutive days
    Intervention: Biological: rh IL-15 (5 DAYS)
  • Experimental: Arm B1 (Dose Escalation, 5-day Dosing)
    MTD determination in subjects with metastatic unresectable cancers receiving rhIL-15 IV for 5 consecutive days
    Intervention: Biological: rh IL-15 (5 DAYS)
  • Experimental: Arm B2 (Dose Expansion, 5-day Dosing)
    Clinical activity evaluation in subjects with metastatic cancers receiving rhIL-15 IV for 5 consecutive days
    Intervention: Biological: rh IL-15 (5 DAYS)
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: August 7, 2018)
38
Original Estimated Enrollment  ICMJE
 (submitted: April 5, 2012)
33
Actual Study Completion Date  ICMJE July 2, 2019
Actual Primary Completion Date June 20, 2018   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE
  • INCLUSION CRITERIA
  • Age greater than or equal to 18 years.
  • Patients must have histologically confirmed (by the NCI Pathology Department) solid tumor malignancy or lymphoma that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are associated with minimal patient survival benefit (as defined the Metabolism Branch physicians or if the patient refuses standard of care treatment ). Enrollment of patients with tumors that can be safely biopsied is encouraged.
  • Patients must have evaluable or measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as greater than or equal to 20 mm with conventional techniques or as greater than or equal to 10 mm with spiral CT scan.
  • Patients must have recovered to < grade 1 CTCAEv4 from toxicity of prior chemotherapy or biologic therapy and must not have had prior chemotherapy or biologic therapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C, 8 weeks for UCN-01).
  • Patients must be at least 1 month since any prior radiation or major surgery.
  • Patients on bisphosphonates for any cancer or on hormone therapy for prostate cancer will not need to discontinue this therapy to be eligible. However, patients with prostate cancer will need to have metastatic prostate cancer that has progressed despite hormonal therapy. Castrate testosterone levels occur within hours after castration and within 2 to 3 weeks of a luteinizing hormone-releasing hormone agonist. The current standard is to continue androgen suppression despite progressive disease.
  • DLCO/VA and FEV-1.0 > 60% of predicted on pulmonary function tests.
  • Serum creatinine of less than or equal to 1.5 X the upper limit of normal.
  • AST and ALT < 2.5 x the upper limit of normal.
  • Absolute neutrophil count greater than or equal to 1,500/mm(3) and platelets greater than or equal to 100,000/mm(3).
  • Karnofsky performance status greater than or equal to 70% or ECOG less than or equal to 1
  • Subjects with inactive central nervous system (CNS) metastasis are eligible. Inactive CNS metastasis is defined as: no signs of cerebral edema after successful definitive treatment of brain metastases (surgical resection, whole brain irradiation, stereotactic radiation therapy, or a combination of these) with stable or improved radiographic appearance on MRI scan at least 1 month after completion of treatment.

EXCLUSION CRITERIA:

  • Patients who have received any systemic corticosteroid therapy within 3 weeks prior to the start of therapy with the exception of physiological replacement doses of cortisone acetate or equivalent.
  • Patients who have received any cytotoxic therapy, immunotherapy, antitumor vaccines, monoclonal antibodies or major surgery in the 4 weeks prior to the start of the study.
  • Life expectancy of less than 3 months.
  • Patients with more than 30% replacement of hepatic parenchyma by tumor or any history of drug related hepatic encephalopathy.
  • History of complex ventricular or supraventricular arrhythmias
  • Documented HIV, active bacterial infections, active or chronic hepatitis B, or hepatitis C infection.
  • A positive hepatitis B serology indicative of previous immunization (i.e., HBsAb positive and HBc Ab negative), or a fully resolved acute hepatitis B infection is not an exclusion criterion.
  • A positive hepatitis C serology is an exclusion criterion.
  • Concurrent anticancer therapy (including other investigational agents), with the exception of hormone therapy for prostate cancer.
  • Active CNS metastases (inactive CNS metastases are defined).
  • History of severe asthma or presently on chronic inhaled corticosteroid medications (patients with a history of mild asthma controlled with inhaled bronchodilators are eligible).
  • History of autoimmune disease, with the exception of an autoimmune event associated with prior ipilimumab (anti-CTLA-4) therapy that has been completely resolved for more than 4 weeks.
  • Inability or refusal to practice effective contraception during therapy or the presence of pregnancy or active breastfeeding (men and women of childbearing potential must use an effective method of birth control or abstinence during treatment and for 4 months after completion of treatment).
  • Cognitive impairment, history of medical or psychiatric disease, other uncontrolled intercurrent illness, active substance abuse, or social circumstances, which in the view of the Principal Investigator (PI), would preclude safe treatment or the ability to give informed consent.
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT01572493
Other Study ID Numbers  ICMJE 120113
12-C-0113
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE Not Provided
Responsible Party National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )
Study Sponsor  ICMJE National Cancer Institute (NCI)
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Kevin C Conlon, M.D. National Cancer Institute (NCI)
PRS Account National Institutes of Health Clinical Center (CC)
Verification Date September 23, 2019

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