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Phase I Trial of Selinexor (KPT-330) and Ifosfamide, Carboplatin, Etoposide (ICE) in Peripheral T-cell Lymphoma

Primary Purpose

Peripheral T-cell Lymphoma

Status
Completed
Phase
Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
Selinexor
ICE Chemotherapy
Sponsored by
National Cancer Centre, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral T-cell Lymphoma

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients must have histologically confirmed T or NK/T-cell lymphomas including the following histologies:

    • Peripheral T-cell lymphoma-not otherwise specified (PTCL-NOS)
    • Angioimmunoblastic T-cell lymphomas (AITL)
    • Anaplastic large cell lymphoma (ALCL)
    • Natural-killer/T-cell lymphoma (NKTL)
  • Patients must have received at least two cycles of one prior regimen administered with curative intent and one of the following:

    • failed to have achieve at least a partial response after 2 or more cycles
    • failed to achieve a complete response after 6 or more cycles
    • progressed after an initial response
    • For patients who have CD30+ anaplastic large cell lymphoma, they must have failed or are ineligible or intolerant of brentuximab vedotin
  • Patients must be age >18 years.
  • Patients must have at least one site of measurable disease, 1.5 cm in diameter or greater.
  • Patients must have ECOG performance status of 0-2
  • Patients must have laboratory test results within these ranges:

    • Absolute neutrophil count ≥1500/mm³
    • Platelet count ≥75,000/mm³
    • Creatinine clearance ≥40ml/min
    • Total bilirubin ≤1.5x ULN. Higher levels are acceptable if these can be attributed to active haemolysis or ineffective erythropoiesis.
    • AST (SGOT) and ALT (SGPT) ≤2x ULN
  • Women of childbearing potential must agree to use dual methods of contraception and have a negative serum pregnancy test prior to KPT-330 treatment. Male patients must use an effective barrier method of contraception if sexually active with a female of child-bearing potential.

    • Acceptable methods of contraception are condoms with contraceptive foam, oral, implantable or injectable contraceptives, contraceptive patch, intrauterine device, diaphragm with spermicidal gel, or a sexual partner who is surgically sterilized or post-menopausal.
    • For both male and female patients, effective methods of contraception must be used throughout the study and for three months following the last dose.

As the effects of selinexor on the developing human fetus at the recommended therapeutic dose are unknown, women of childbearing potential should be advised to avoid becoming pregnant and men should be advised to not father a child while receiving treatment with selinexor. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately. Women that are pregnant or breastfeeding are excluded from the study because the risks to an unborn fetus or potential risks in nursing infants are unknown.

  • Patients must be able to understand and willing to sign a written informed consent document.
  • Patients must be able to adhere to the study visit schedule and other protocol requirements.
  • Patients must not have any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
  • Patients must not have any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study.

Exclusion Criteria:

  • Patients who have had prior malignancies (other than T and NK/T-cell lymphomas) for ≤5 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in situ" of the cervix or breast.
  • Patients who have had other anti-cancer therapy, including radiation or experimental drug or therapy, within 28 days of enrollment.
  • Patients with known HIV, active hepatitis B, active hepatitis C.
  • Patients with known central nervous system involvement by lymphoma.
  • Patients with known or suspected hypersensitivity to selinexor.

Inclusion of Women and Minorities:

Men and women of all ethnic groups are eligible for this study

Sites / Locations

  • National Cancer Centre Singapore

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Selinexor and ICE Chemotherapy

Arm Description

Outcomes

Primary Outcome Measures

Number of participants with treatment related dose limiting toxicity as assessed by NCI CTCAE v4.0

Secondary Outcome Measures

Overall response rate
Responses will be assessed using the revised International Workshop Criteria
Progression-free survival
Overall survival

Full Information

First Posted
June 28, 2017
Last Updated
April 27, 2021
Sponsor
National Cancer Centre, Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT03212937
Brief Title
Phase I Trial of Selinexor (KPT-330) and Ifosfamide, Carboplatin, Etoposide (ICE) in Peripheral T-cell Lymphoma
Official Title
A Phase I Investigator Sponsored Trial of Selinexor (KPT-330), a Selective Inhibitor of Nuclear Export / SINE™ Compound and Ifosfamide, Carboplatin, Etoposide (ICE) in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
July 1, 2016 (Actual)
Primary Completion Date
November 2020 (Actual)
Study Completion Date
November 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Cancer Centre, Singapore

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a single center, open-label, phase I trial with a standard 3+3 dose escalation schema to identify the maximum tolerated dose (MTD) of selinexor when combined with ICE. Once MTD is determined, there will be an expansion phase and tumor biopsies and peripheral blood will be taken pre and post selinexor to examine the study's biologic objectives.
Detailed Description
STUDY OBJECTIVES: Primary: • To determine the maximum tolerated dose (MTD) of selinexor when given in combination with a standard dose regimen of ifosfamide, carboplatin and etoposide (ICE) in patients with relapsed or refractory PTCL Secondary: To assess the response rates (complete and partial), progression-free survival (PFS) and overall survival (OS) in patients with relapsed or refractory PTCL To estimate the feasibility of stem cell collection after selinexor and ICE Laboratory objectives: • Paired tumor specimens pre and post selinexor will be examined ex vivo for Response to chemotherapy agents such as doxorubicin and etoposide Nuclear localization of tumor suppressor proteins (p53, p73, FOXO), drug targets (topoisomerase II) and mRNA targets STUDY DESIGN: This is a single center, open-label, phase I trial with a standard 3+3 dose escalation schema to identify the maximum tolerated dose (MTD) of selinexor when combined with ICE. Once MTD is determined, there will be an expansion phase and tumor biopsies and peripheral blood will be taken pre and post selinexor to examine the study's biologic objectives. Dose escalation: If 0/3 dose-limiting toxicity (DLT) is observed, dose escalation will continue to the next higher dose level. If 1/3 DLT is observed, then 3 additional patients will be enrolled in the same dose level; if no DLT is observed from the additional 3 patients, then dose escalation will continue to the next higher dose level. If any DLT is observed from the additional 3 patients, then the previous lower dose will be chosen as the MTD. If ≥ 2/3 DLTs are observed, then the previous lower dose level will be chosen as the MTD and the dose finding procedure will be terminated. PATIENTS: Subjects will be enrolled at the National Cancer Centre Singapore (NCCS). Key eligibility criteria include the following: Pathologically confirmed aggressive T-cell lymphomas including the following histologies: PTCL-NOS, AITL, ALCL (independent of ALK status), NK/T-cell lymphoma Treatment with at least two cycles of one prior regimen administered with curative intent Adequate end-organ and bone marrow function Absence of known or suspected CNS involvement Absence of active viral hepatitis or uncontrolled HIV STUDY DURATION: Based on prior and existing patient volumes and accrual to clinical trials, we expect to enroll 1-2 patients per month. We expect to complete study accrual within 2 years. TOTAL SAMPLE SIZE: The MTD will be identified using a standard 3+3. A maximum of 18 patients will be required for this phase I study. An additional 5 patients will be treated at the recommended phase II dose to assess safety and to examine the study's biologic objectives. DOSING REGIMEN: Dose escalation schedule for selinexor: Dose level -1: 20mg Dose level 1: 40mg Dose level 2: 60mg Dose level 3: 80mg Selinexor will be administered on days 3, 5 and 7 of each chemotherapy cycle and ICE will be administered from day 1. In the expansion phase of the study, selinexor is administered on days -5 and -3 prior to cycle 1 of chemotherapy. All subjects will receive (I) Standard dose ICE on a 21-day cycle. IV Etoposide 100mg/m^2 on D1-3 IV Carboplatin AUC 5 on D2 (inpatient) or D1 (outpatient) IV Ifosfamide 5g/m^2 on D2 (inpatient) or D1-3 (outpatient) (II) Dexamethasone 20mg QD D3-7 20mg QD D-5 and D-3 (for patients in the expansion phase) Patients will receive 2-6 cycles of selinexor and ICE. If determined eligible by their treating physician, patients who demonstrate response will undergo autologous stem cell transplantation anytime following the second cycle of selinexor and ICE. Transplant ineligible patients will complete up to 6 cycles of selinexor and ICE, and those with responses or stable disease are eligible for maintenance selinexor at the discretion of the treating physician. Maintenance selinexor will be administered weekly at the dose of 60mg. Dexamethasone 4-12mg should also be given on the selinexor dosing days. ASSESSMENT: CT Neck to pelvis or FDG-PET/CT skull base to mid-thigh to be performed repeated after every 2 cycles on days 17 +/- 3 days except after cycle 2 where FDG-PET/CT will be performed

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral T-cell Lymphoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Selinexor and ICE Chemotherapy
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Selinexor
Intervention Description
Oral KPT-330 is administered on Day 3, 5, and 7 of each 21-day cycle. Starting dose is 40mg will be adjusted according to toxicity
Intervention Type
Drug
Intervention Name(s)
ICE Chemotherapy
Other Intervention Name(s)
Ifosfamide, Carboplatin, Etoposide
Intervention Description
IV Ifosfamide 5g/m^2 on Day 2 (inpatient) or D1 (outpatient) of each 21-day cycle IV Carboplatin AUC 5 on Day 2 (inpatient) or D1-3 (outpatient) of each 21-day cycle IV Etoposide 100 mg/m^2 on Days 1-3 of each 21-day cycle
Primary Outcome Measure Information:
Title
Number of participants with treatment related dose limiting toxicity as assessed by NCI CTCAE v4.0
Time Frame
The first 3 weeks of treatment
Secondary Outcome Measure Information:
Title
Overall response rate
Description
Responses will be assessed using the revised International Workshop Criteria
Time Frame
From the start of treatment to the best overall response of Complete or Partial Response is achieved, up to 2 years
Title
Progression-free survival
Time Frame
From the start of the treatment to the date of documentation of either disease progression or death, up to 2 years
Title
Overall survival
Time Frame
From the start of treatment to the date of death from any cause, up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have histologically confirmed T or NK/T-cell lymphomas including the following histologies: Peripheral T-cell lymphoma-not otherwise specified (PTCL-NOS) Angioimmunoblastic T-cell lymphomas (AITL) Anaplastic large cell lymphoma (ALCL) Natural-killer/T-cell lymphoma (NKTL) Patients must have received at least two cycles of one prior regimen administered with curative intent and one of the following: failed to have achieve at least a partial response after 2 or more cycles failed to achieve a complete response after 6 or more cycles progressed after an initial response For patients who have CD30+ anaplastic large cell lymphoma, they must have failed or are ineligible or intolerant of brentuximab vedotin Patients must be age >18 years. Patients must have at least one site of measurable disease, 1.5 cm in diameter or greater. Patients must have ECOG performance status of 0-2 Patients must have laboratory test results within these ranges: Absolute neutrophil count ≥1500/mm³ Platelet count ≥75,000/mm³ Creatinine clearance ≥40ml/min Total bilirubin ≤1.5x ULN. Higher levels are acceptable if these can be attributed to active haemolysis or ineffective erythropoiesis. AST (SGOT) and ALT (SGPT) ≤2x ULN Women of childbearing potential must agree to use dual methods of contraception and have a negative serum pregnancy test prior to KPT-330 treatment. Male patients must use an effective barrier method of contraception if sexually active with a female of child-bearing potential. Acceptable methods of contraception are condoms with contraceptive foam, oral, implantable or injectable contraceptives, contraceptive patch, intrauterine device, diaphragm with spermicidal gel, or a sexual partner who is surgically sterilized or post-menopausal. For both male and female patients, effective methods of contraception must be used throughout the study and for three months following the last dose. As the effects of selinexor on the developing human fetus at the recommended therapeutic dose are unknown, women of childbearing potential should be advised to avoid becoming pregnant and men should be advised to not father a child while receiving treatment with selinexor. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately. Women that are pregnant or breastfeeding are excluded from the study because the risks to an unborn fetus or potential risks in nursing infants are unknown. Patients must be able to understand and willing to sign a written informed consent document. Patients must be able to adhere to the study visit schedule and other protocol requirements. Patients must not have any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form. Patients must not have any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study. Exclusion Criteria: Patients who have had prior malignancies (other than T and NK/T-cell lymphomas) for ≤5 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in situ" of the cervix or breast. Patients who have had other anti-cancer therapy, including radiation or experimental drug or therapy, within 28 days of enrollment. Patients with known HIV, active hepatitis B, active hepatitis C. Patients with known central nervous system involvement by lymphoma. Patients with known or suspected hypersensitivity to selinexor. Inclusion of Women and Minorities: Men and women of all ethnic groups are eligible for this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tiffany PL Tang
Organizational Affiliation
National Cancer Centre, Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cancer Centre Singapore
City
Singapore
ZIP/Postal Code
169610
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Phase I Trial of Selinexor (KPT-330) and Ifosfamide, Carboplatin, Etoposide (ICE) in Peripheral T-cell Lymphoma

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