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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/NCT02314247
Registration number
NCT02314247
Ethics application status
Date submitted
3/12/2014
Date registered
11/12/2014
Date last updated
26/01/2023
Titles & IDs
Public title
Efficacy and Safety Study of Selinexor in Relapsed or Refractory Peripheral T-cell Lymphoma or Cutaneous T-cell Lymphoma
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Scientific title
Multi-center, Phase 2, Open-label Study of Efficacy and Safety of the Selective Inhibitor of Nuclear Export (SINE™) Selinexor (KPT-330) in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL) and Cutaneous T-cell Lymphoma (CTCL)
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Secondary ID [1]
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KCP-330-013
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Peripheral T-cell Lymphoma (PTCL)
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Cutaneous T-cell Lymphoma (CTCL)
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Condition category
Condition code
Cancer
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Lymphoma (non Hodgkin's lymphoma) - High grade lymphoma
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Cancer
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Lymphoma (non Hodgkin's lymphoma) - Low grade lymphoma
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Selinexor
Experimental: Selinexor - 60 mg dose (equivalent to ~35 mg/m²)
Treatment: Drugs: Selinexor
20 mg oral tablets: 60 mg dose on Days 1 and 3 of Weeks 1-4 of each 4-week cycle (Protocol V.3.0).
20 mg oral tablets: 60 mg dose on Days 1 and 3 of Weeks 1-3 of each 4-week cycle (Protocol V.<3.0).
Number of Cycles: up to 12 but there is no maximal duration for treatment.
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Intervention code [1]
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Treatment: Drugs
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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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Overall Response Rate (ORR)
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Assessment method [1]
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Overall Response (OR) = Complete Response (CR) + Partial Response (PR). Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment. Progression was defined as the first occurrence of progressive disease (PD) per the revised response criteria. Clinical disease progression in the absence of formal criteria for PD must be documented by a physician.
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Timepoint [1]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Primary outcome [2]
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Best Overall Response: Complete Response (CR)
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Assessment method [2]
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Patients who achieved CR (disappearance of all detectable evidence of disease). Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment.
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Timepoint [2]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Primary outcome [3]
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Best Overall Response: Partial Response (PR)
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Assessment method [3]
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Patients whose best overall response to study treatment was PR (regression of measurable disease and no new sites). Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment.
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Timepoint [3]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Primary outcome [4]
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Best Overall Response: Stable Disease (SD)
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Assessment method [4]
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Patients whose best overall response to study treatment was SD (failure to attain criteria needed for CR or PR, or to meet criteria for PD). Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment.
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Timepoint [4]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Primary outcome [5]
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Best Overall Response: Progressive Disease (PD)
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Assessment method [5]
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Patients whose best overall response to study treatment was PD. Progression was defined as the first occurrence of progressive disease (PD). Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment. Clinical disease progression in the absence of formal criteria for PD must be documented by a physician.
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Timepoint [5]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Primary outcome [6]
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Best Overall Response: Not Evaluable (NE)
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Assessment method [6]
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Patients who could not be assessed quantitatively for disease response for any reason.
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Timepoint [6]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Secondary outcome [1]
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Duration of Stable Disease, Including Patients With Partial Response
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Assessment method [1]
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Duration of time from the date of start of study treatment to the date of disease progression. Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment.
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Timepoint [1]
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Date of start of study treatment to date of progression. Patients without documented PD are censored on date of last radiologic assessment.
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Secondary outcome [2]
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Disease Control Rate (DCR)
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Assessment method [2]
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Percentage of patients who have CR, PR, or SD lasting = 8 weeks. Objective disease response assessment in PTCL patients was made according to the revised response criteria based on the International Working Group (IWG) guidelines for malignant lymphoma (Cheson, 2007). Objective disease response assessment in CTCL patients was assessed according to the revised CTCL Consensus Response Criteria (Olsen, 2011) using physical examination, including the Modified Severity Weighted Assessment Tool (mSWAT) for skin assessment. CTCL Global Response Score was used as a secondary efficacy assessment.
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Timepoint [2]
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Disease response was assessed at screening and every 8 weeks (patients with PTCL); or at Cycle 1 Day 1 and every 4 weeks (patients with CTCL), until disease progression.
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Secondary outcome [3]
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Progression Free Survival (PFS)
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Assessment method [3]
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Duration of time from start of study treatment to date of disease progression or death from any cause.
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Timepoint [3]
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Study treatment start date to date of disease progression or date of death. Patients without documented PD are censored on date of last radiologic assessment.
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Eligibility
Key inclusion criteria
- ECOG performance status of =2.
- Relapsed or refractory disease to at least one prior systemic regimen.
- Measurable disease: according to International Working Group (IWG) guidelines for all
patients with PTCL and according to CTCL Response in Skin consensus criteria for all
patients with CTCL.
- Objective, documented evidence of disease progression on study entry.
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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
- Known active central nervous system (CNS) lymphoma.
- Active graft-versus-host disease after allogeneic stem cell transplantation. At least
4 months must have elapsed since completion of allogeneic stem cell transplantation.
- Unable to swallow tablets or malabsorption syndrome, disease significantly affecting
gastrointestinal function.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
N/A
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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
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Terminated
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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
1/02/2015
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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
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Actual
1/02/2016
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Sample size
Target
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Accrual to date
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Final
16
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Recruitment in Australia
Recruitment state(s)
NSW,VIC
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Recruitment hospital [1]
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Concord Repatriation General Hospital (CRGH) - Concord
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Recruitment hospital [2]
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Royal North Shore Hospital - St. Leonards
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Recruitment hospital [3]
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Westmead Hospital - Westmead
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Recruitment hospital [4]
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Cabrini Hospital - Malvern
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Recruitment postcode(s) [1]
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2139 - Concord
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Recruitment postcode(s) [2]
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2139 - St. Leonards
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Recruitment postcode(s) [3]
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2145 - Westmead
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Recruitment postcode(s) [4]
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- Malvern
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Recruitment outside Australia
Country [1]
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Singapore
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State/province [1]
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Singapore
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Karyopharm Therapeutics Inc
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This is a single-arm, multi-center, open-label phase 2 study of the SINE™ compound selinexor
given orally to patients with relapsed or refractory PTCL or CTCL.
Approximately 60 patients with relapsed or refractory PTCL or CTCL who meet the eligibility
criteria and have none of the exclusion criteria will be enrolled to receive selinexor until
either disease progression or intolerance has occurred.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT02314247
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
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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 public queries
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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/NCT02314247
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