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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT02504372
Registration number
NCT02504372
Ethics application status
Date submitted
20/07/2015
Date registered
21/07/2015
Date last updated
30/03/2023
Titles & IDs
Public title
Study of Pembrolizumab (MK-3475) vs Placebo for Participants With Non-small Cell Lung Cancer After Resection With or Without Standard Adjuvant Therapy (MK-3475-091/KEYNOTE-091)
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Scientific title
A Randomized, Phase 3 Trial With Anti-PD-1 Monoclonal Antibody Pembrolizumab (MK-3475) Versus Placebo for Patients With Early Stage NSCLC After Resection and Completion of Standard Adjuvant Therapy (PEARLS)
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Secondary ID [1]
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EORTC-1416-LCG
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Secondary ID [2]
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3475-091
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Universal Trial Number (UTN)
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Trial acronym
PEARLS
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Non-small Cell Lung Cancer
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Condition category
Condition code
Cancer
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Lung - Mesothelioma
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Cancer
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Lung - Non small cell
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Cancer
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Lung - Small cell
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Other interventions - pembrolizumab
Other interventions - Placebo
Experimental: Pembrolizumab - Participants receive pembrolizumab 200 mg, intravenously (IV), every 3 weeks, for one year (expected maximum 18 doses).
Placebo Comparator: Placebo - Participants receive placebo, IV, every 3 weeks, for one year (expected maximum 18 doses).
Other interventions: pembrolizumab
Other interventions: Placebo
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Intervention code [1]
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Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Disease-free Survival (DFS)
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Assessment method [1]
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Timepoint [1]
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Up to approximately 78 months
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Secondary outcome [1]
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Overall Survival (OS)
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Assessment method [1]
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Timepoint [1]
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Up to approximately 111 months
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Secondary outcome [2]
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Lung Cancer Specific Survival (LCSS)
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Assessment method [2]
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Timepoint [2]
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Up to approximately 111 months
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Eligibility
Key inclusion criteria
- Pathological diagnosis of NSCLC confirmed at surgery, any histology. Participants with
two synchronous primary non-small cell lung cancers are excluded from the study
- Union for International Cancer Control (UICC) v7 Stage IB with T = 4 cm, II-IIIA NSCLC
after complete surgical resection with resection margins proved microscopically free
of disease (R0). Carcinoma in situ can be present at the bronchial margin
- Available tumor sample obtained at surgical resection for programmed cell death
ligand-1 (PD-L1) Immunohistochemistry (IHC) expression assessment
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1
- Adequate organ function performed within 10 days of treatment initiation
- Female participants of childbearing potential must have a negative urine or serum
pregnancy test at screening (within 72 hours of first infusion of study medication).
If the urine test cannot be confirmed as negative, a serum pregnancy test will be
required. The serum pregnancy test must be negative for the participant to be eligible
- Female participants of childbearing potential must be willing to use 2 methods of
birth control or be surgically sterile, or abstain from heterosexual activity starting
with the first infusion of study treatment through 120 days after the last infusion of
study treatment
- Female participants who are breast feeding must discontinue nursing prior to the first
infusion of study medication and until 120 days after the last infusion study
treatment
- Male participants must agree to use an adequate method of contraception starting with
the first infusion of study treatment through 120 days after the last infusion of
study treatment
- Absence of severe comorbidities that in the opinion of the Investigator might hamper
the participation to the study and/or the treatment administration
- No prior or planned neo-adjuvant or adjuvant radiotherapy and/or neo-adjuvant
chemotherapy for the current malignancy is allowed
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
- Evidence of disease at clinical examination and/or baseline radiological assessment as
documented by contrast enhanced chest/upper abdomen CT scan, brain CT/MRI and clinical
examination
- More than 4 cycles of adjuvant therapy
- Prior treatment with anti-programmed cell death (anti-PD)-1, anti-PD ligand-1/2,
anti-CD137, or cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) modulators or any
other immune-modulating agents
- Live vaccine within 30 days prior to the first infusion of study treatment
- Current participation or treatment with an investigational agent or use of an
investigational device within 4 weeks of the first infusion of study treatment
- History of Human Immunodeficiency Virus (HIV) (known HIV 1/2 antibodies positive). No
known active Hepatitis B or C
- Chronic use of immunosuppressive agents and/or systemic corticosteroids or any use in
the last 3 days prior to the first infusion of study treatment
- History of interstitial lung disease or (non-infectious) pneumonitis that required
oral or IV steroids (other than COPD exacerbation) or current pneumonitis
- Active autoimmune disease that has required systemic treatment in past 2 years
- History of a hematologic or primary solid tumor malignancy, unless in remission for at
least 5 years with the exception of pT1-2 prostatic cancer Gleason score < 6,
superficial bladder cancer, non melanomatous skin cancer or carcinoma in situ of the
cervix
- Previous allogeneic tissue/solid organ transplant
- Active infection requiring therapy
- Surgery- or chemotherapy-related toxicity (non-hematological) not resolved to Grade 1
with the exception of alopecia, fatigue, neuropathy and lack of appetite /nausea
- Pregnant or breastfeeding, or expecting to conceive or father children within the
projected duration of the trial, starting with the screening visit through 120 days
after the last infusion of study treatment
- Participant will not be eligible if the participant is or has an immediate family
member (e.g., spouse, parent/legal guardian, sibling or child) who is investigational
site or Sponsor staff directly involved with this trial, unless prospective site
Review Board approval is given allowing exception to this criterion for a specific
participant
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
6/11/2015
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
2/02/2024
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Actual
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Sample size
Target
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Accrual to date
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Final
1177
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Merck Sharp & Dohme LLC
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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ETOP
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Address [1]
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Country [1]
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Other collaborator category [2]
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Other
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Name [2]
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European Organisation for Research and Treatment of Cancer - EORTC
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Address [2]
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Ethics approval
Ethics application status
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Summary
Brief summary
In this study, participants with Stage IB/II-IIIA non-small cell lung cancer (NSCLC) who have
undergone surgical resection (lobectomy or pneumonectomy) with or without adjuvant
chemotherapy will be treated with pembrolizumab or placebo. The primary study hypothesis is
that pembrolizumab will provide improved disease-free survival (DFS) versus placebo.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT02504372
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Trial related presentations / publications
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Public notes
This record is viewable in the ANZCTR as it had previously listed Australia and/or New Zealand as a recruitment site, however these sites have since been removed
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Contacts
Principal investigator
Name
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Medical Director
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Address
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Merck Sharp & Dohme LLC
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT02504372
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