Clinical Trials /

A Study of Abemaciclib (LY2835219) in Participants With Previously Treated KRAS Mutated Lung Cancer

NCT02152631

Description:

The main purpose of this study is to evaluate how safe and effective the study drug known as abemaciclib is in participants with lung cancer.

Related Conditions:
  • Non-Small Cell Lung Carcinoma
Recruiting Status:

Active, not recruiting

Phase:

Phase 3

Trial Eligibility

Document

Title

  • Brief Title: A Study of Abemaciclib (LY2835219) in Participants With Previously Treated KRAS Mutated Lung Cancer
  • Official Title: JUNIPER: A Randomized Phase 3 Study of Abemaciclib Plus Best Supportive Care Versus Erlotinib Plus Best Supportive Care in Patients With Stage IV NSCLC With a Detectable KRAS Mutation Who Have Progressed After Platinum-Based Chemotherapy

Clinical Trial IDs

  • ORG STUDY ID: 15296
  • SECONDARY ID: I3Y-MC-JPBK
  • SECONDARY ID: 2013-004662-33
  • NCT ID: NCT02152631

Conditions

  • Non Small Cell Lung Cancer

Interventions

DrugSynonymsArms
AbemaciclibLY2835219Abemaciclib
ErlotinibErlotinib

Purpose

The main purpose of this study is to evaluate how safe and effective the study drug known as abemaciclib is in participants with lung cancer.

Trial Arms

NameTypeDescriptionInterventions
AbemaciclibExperimental200 milligrams (mg) abemaciclib administered, orally, every 12 hours plus best supportive care (BSC) on Days 1 to 28 (28 day cycles).
  • Abemaciclib
ErlotinibActive Comparator150 mg erlotinib administered, orally, every 24 hours plus BSC on Days 1 to 28 (28 day cycles).
  • Erlotinib

Eligibility Criteria

        Inclusion Criteria:

          -  Have confirmed diagnosis of stage IV non-small cell lung cancer (NSCLC) according to
             the American Joint Committee on Cancer Staging Handbook.

          -  Determined to have detectable mutations in codons 12 or 13 of the kirsten rat sarcoma
             (KRAS) oncogene by an investigational assay at the study central laboratory. A KRAS
             positive mutation result in codons 12 or 13 of the KRAS oncogene from tumor tissue per
             local laboratory will be permitted in no more than 10% of randomized participants.

          -  Have progressed after platinum-based chemotherapy (with or without maintenance
             therapy) AND have received one additional therapy which may include an immune
             checkpoint inhibitor or other anti-cancer therapy for advanced and/or metastatic
             disease OR is judged by the physician as ineligible for further standard second-line
             chemotherapy. Participants who have progressed after platinum-based chemotherapy and
             an immune checkpoint inhibitor (immunotherapy) e.g. pembrolizumab or nivolumab alone
             or in combination with other agents are eligible.

          -  Have measureable disease as defined by the Response Evaluation Criteria in Solid
             Tumors (RECIST 1.1).

          -  Have a performance status (PS) of 0 to 1 on the Eastern Cooperative Oncology Group
             (ECOG) scale.

          -  Have discontinued all previous therapies for cancer (including chemotherapy,
             radiotherapy, immunotherapy, and investigational therapy) for at least 21 days for
             myelosuppressive agents or 14 days for nonmyelosuppressive agents prior to receiving
             study drug.

        Exclusion Criteria:

          -  Have received treatment with a drug that has not received regulatory approval for any
             indication within 14 or 21 days of the initial dose of study drug for a
             nonmyelosuppressive or myelosuppressive agent, respectively.

          -  Have a personal history of any of the following conditions: presyncope or syncope of
             either unexplained or cardiovascular etiology, ventricular arrhythmia (including but
             not limited to ventricular tachycardia and ventricular fibrillation), or sudden
             cardiac arrest.

          -  Have the presence of unstable central nervous system (CNS) metastasis. History of CNS
             metastasis or stable CNS metastases is allowed (no longer requiring active therapy
             such as steroid medications). Participants with a history of CNS metastases must have
             a brain scan (for example, magnetic resonance imaging [MRI]) within 28 days of
             randomization to document stability, even if there have been no changes in symptoms.

          -  Have previously completed or withdrawn from this study or any other study
             investigating a cyclin-dependent kinase 4 (CDK4) and cyclin-dependent kinase 6 (CDK6)
             inhibitors, or have received treatment with a prior CDK4 and CDK6 inhibitors.
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Overall Survival (OS)
Time Frame:From Randomization Date to Date of Death from Any Cause (Up to 32 Months)
Safety Issue:
Description:OS defined as from randomization date to the date of death due to any cause. For each participant who is not known to have died as of the data-inclusion cutoff date for overall survival analysis, OS time was censored on the last date the participant is known to be alive.

Secondary Outcome Measures

Measure:Percentage of Participants With Complete Response (CR) or Partial Response (PR) (Objective Response Rate [ORR])
Time Frame:From Randomization Date to Objective Progression (Up to 32 Months)
Safety Issue:
Description:ORR was the percentage of participants achieving a best overall response (BOR) of complete response (CR) or partial response (PR) as per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. CR defined as the disappearance of all target and non-target lesions and no appearance of new lesions. PR defined as at least a 30% decrease in the sum of the longest diameters (LD) of target lesions (taking as reference the baseline sum LD), no progression of non-target lesions, and no appearance of new lesions.
Measure:Progression Free Survival (PFS)
Time Frame:From Randomization Date until Disease Progression or Death from Any Cause (Up to 32 Months)
Safety Issue:
Description:PFS defined as the from randomization date to the first evidence of disease progression as defined by RECIST v1.1 or death from any cause. Progressive Disease (PD) was at least a 20% increase in the sum of the diameters of target lesions, with reference being the smallest sum on study and an absolute increase of at least 5 mm, or unequivocal progression of non-target lesions, or 1 or more new lesions. If a participant does not have a complete baseline disease assessment, then the PFS time was censored at the date of first dose, regardless of whether or not objectively determined disease progression or death has been observed for the participant. If a participant was not known to have died or have objective progression as of the data inclusion cutoff date for the analysis, the PFS time was censored at the last adequate tumor assessment date.
Measure:Change From Baseline in MD Anderson Symptom Inventory-Lung Cancer (MDASI-LC) Score
Time Frame:From Randomization Date through End of Study (Up to 32 Months)
Safety Issue:
Description:The MDASI-LC included 22 items + 3 additional trial-specific items, resulting in 6 collected and reported single-construct scores including core symptoms (13-item), interference (6-item), lung cancer (3-item), and trial-specific single outcomes for headache, diarrhea, and rash. A 2-construct composite core + lung cancer symptom (16-item) score was calculated. Data for all 7 scores were collected by an 11-point numeric rating scale anchored at 0 (not present or does not interfere) and 10 (as bad as you can imagine or interfered completely). The measurement range was 10 (maximum score-minimum score). Mixed Model Repeated Measure (MMRM) regression with covariates for treatment, visit, treatment*visit, and baseline score predicted between-group Least Squares (LS) mean differences from baseline. Group-level negative change from baseline indicated group improvement.
Measure:Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve During 1 Dosing Interval at Steady State
Time Frame:Day 1 of Cycle 1 through Cycle 3 (28 Day Cycles)
Safety Issue:
Description:PK is determined by the area under the plasma concentration versus time curve during 1 dosing interval at steady state
Measure:Change From Baseline in European Quality of Life - 5 Dimensions - 5 Level (EQ-5D-5L) Score
Time Frame:From Randomization Date through End of Study (Up to 32 Months)
Safety Issue:
Description:There are 5 response levels on a good-to-bad continuum of 1-5 corresponding to none, slight, moderate, severe, and extreme/unable to. The EuroQol-developed crosswalk method was used to convert the EQ-5D-5L,using United Kingdom (UK) weights, health dimensions(mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) into a single index value; the dimensions are not separately scored. The index is marked missing when ≥1 dimensions are missing. The index scores for the response patterns were anchored on full health to dead with negative values assigned to response patterns/health states considered worse than death. The best pattern is assigned the index value of 1.0; the worst pattern is assigned an index value of -0.594. Between-group differences in regression-predicted change from baseline score were estimated for the index. LS Mean value was controlled for Treatment, visit, Treatment*Visit and baseline.
Measure:Resource Utilization: Percentage of Participants Who Are Hospitalized
Time Frame:From Randomization Date through End of Study (Up to 32 Months)
Safety Issue:
Description:Resource utilization is the percentage of participants who was hospitalized.

Details

Phase:Phase 3
Primary Purpose:Interventional
Overall Status:Active, not recruiting
Lead Sponsor:Eli Lilly and Company

Trial Keywords

  • Therapy, Platinum, Kras +

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