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Phase II Study of Carfilzomib, Pomalidomide, and Dexamethasone for Myeloma Patients Who Had Relapsed or Progressed After Carfilzomib, Lenalidomide, and Dexamethasone (KMM2002)

Primary Purpose

Multiple Myeloma

Status
Recruiting
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Carfilzomib 56 MG [Kyprolis]
Pomalidomide
Dexamethasone
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Myeloma

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age from 20 to 80 years-old
  2. Relapse or progression of multiple myeloma after treatment of carfilzomib/lenalidomide/dexamethasone (KRd)
  3. KRd treatment 12 cycles or more and lenalidomide maintenance for at least 6 months or KRd 4-6 cycles followed by ASCT and lenalidomide maintenance for at least 6 months
  4. Measurable disease

    • Serum M-protein ≥ 1 g/dL (10 g/L)
    • Urine M-protein ≥ 200 mg/24 hr
    • Serum FLC assay: difference of FLC ≥ 10 mg/dL (100 mg/L) provided serum FLC ratio is abnormal (KL ratio < 0.26 or > 1.65) if Serum EP or urine EP is not measurable
  5. Adequate organ functions

    • Absolute Neutrophil Count (ANC) ≥ 1.0 x 109/L
    • Platelets ≥ 50 x 109/L (≥ 30 x 109/L if myeloma involvement is > 50% in the bone marrow)
    • Hemoglobin ≥ 8.0 g/dL
    • Creatinine clearance ≥ 30 mL/minute or Serum Cr <3.0 g/dL
    • Serum Bilirubin ≤ 1.5 x ULN
    • AST and ALT ≤ 3 x ULN
  6. Eastern Cooperative Oncology Group performance scale 0~2
  7. Life expectancy longer than 3 months
  8. Written informed consent
  9. Prior therapy with bortezomib
  10. Patients who meet the following criteria

    • If a woman of childbearing age

      • Women who are willing to use two reliable methods of contraception from 4 weeks prior to administration of study drug, while receiving, temporarily suspending administration, and 4 weeks after administration of the study drug.
      • Women who have a negative pregnancy test with a minimum sensitivity of 25 IU/mL under medical management
    • For men Men who agree to abstain from absolute abstinence or use a proper method of contraception for the entire duration of treatment and 28 days after the last dose

      • Women of childbearing age Women who have not undergone hysterectomy or bilateral oophorectomy, women who have not undergone spontaneous menopause for at least 24 consecutive months (i.e., menstruate at any time during the last 24 months. However, amenorrhea after chemotherapy does not exclude the possibility of pregnancy).
      • Proper method of contraception
    • Very effective way Intrauterine device, hormone therapy (hormone implant, intrauterine system releasing levonorgestrel, medroxyprogesterone acetate depot injection, tablets containing progesterone to inhibit ovulation), tubal ligation, varicose veins in men
    • Effective way Men's condom use, diaphragm method, cervical cap

Exclusion Criteria:

  1. Grade 3~4 non-hematologic toxicity by carfilzomib during the previous carfilzomib treatment
  2. Prior therapy with pomalidomide
  3. Hypersensitivity to thalidomide or lenalidomide
  4. Previous refractoriness to carfilzomib according to the IMWG criteria
  5. Myocardial infarct within 6 months, heart failure of NYHA Class III~IV, uncontrolled ventricular arrhythmia, severe coronary arterial obstructive disease
  6. Active infection with 14 days prior to treatment
  7. Uncontrolled hypertension (Defined as an average systolic blood pressure >= 160 mmHg or diastolic >= 100 mmHg) or diabetes (HbA1c > 7.0%)
  8. HIV, HBV, HCV infection (exception if adequately controlled HBV (undetectable HBV DNA (< 20 IU/mL or concurrent use of an anti-viral agent), HCV)
  9. Severe or uncontrolled medical conditions, laboratory abnormalities, or psychiatric disorders that may preclude the participation of the study by the physician's discretion
  10. Contraindication to any of the required concomitant drugs or supportive treatments, including hypersensitivity to all anticoagulation and antiplatelet options, antiviral drugs, or intolerance to hydration due to preexisting pulmonary or cardiac impairment
  11. Diagnosis of other malignant disease other than myeloma within 5 year. Exceptions are properly treated non-melanomatous skin cancers, cervical intraepithelial neoplasia, prostate cancer that do not require treatment, or properly excised well-differentiated thyroid cancers.
  12. Pregnant or nursing women
  13. Waldenstroem's macroglobulinemia, POEMS syndrome, or plasma cell leukemia, light chain amyloidosis
  14. LV ejection fraction < 40%

Sites / Locations

  • Samsung Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A study of carfilzomib, pomalidomide and dexamethasone administration after KRd administration

Arm Description

Patients with RRMM who progressed after receiving lenalidomide monotherapy for at least 6 months after administration of KRd will receive KPD therapy every 4 weeks until disease progression.

Outcomes

Primary Outcome Measures

Overall response rate
percentage of patients who achieve at least partial response

Secondary Outcome Measures

Complete response rate
percentage of patients who achieve complete response
Progression free survival rate
percentage of patients who are disease free or alive
Overall survival
from the time of written consent to the time of death or last follow-up
Duration of response
from the time of achieving at least partial response to the time of progressive disease
Time to response
from the time of written consent to the time of achieving at least partial response
Incidence of treatment-emergent adverse events
Safety profiles of carfilzomib, pomalidomide, and dexamethasone for myeloma patients who had relapsed or progressed
Minimal residual disease negativity
The specimen is bone marrow aspirate, and it should be free of clonal plasma cells by examination by the NGF (next-generation flow) method. At this time, the test should be performed according to the EuroFlow standard operation procedure for MRD detection in MM, and the minimum sensitivity should be10 to the 5th power or higher.

Full Information

First Posted
August 18, 2022
Last Updated
August 19, 2022
Sponsor
Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05509374
Brief Title
Phase II Study of Carfilzomib, Pomalidomide, and Dexamethasone for Myeloma Patients Who Had Relapsed or Progressed After Carfilzomib, Lenalidomide, and Dexamethasone
Acronym
KMM2002
Official Title
Phase II, Single-arm Trial of Carfilzomib, Pomalidomide, and Dexamethasone for Myeloma Patients Who Had Relapsed or Progressed After Carfilzomib, Lenalidomide, and Dexamethasone
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 28, 2021 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center

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
The purpose of this study is to evaluate the evaluate the efficacy and safety of administering a combination of carfilzomib, pomalidomide, and dexamethasone in patients with relapsed or advanced multiple myeloma after carfilzomib, lenalidomide, and dexamethasone therapy.
Detailed Description
This study is a phase 2 study in which patients with RRMM under 80 years of age who have been treated with lenalidomide monotherapy for at least 6 months after KRd combination therapy will receive carfilzomib, pomalidomide, and dexamethasone combination therapy. A total of 33 participants are recruited. KPd will be administered until progressive disease or unacceptable toxicities. Participants who discontinued treatment will be followed up for disease status and survival at 2-month intervals. Responses are assessed using the International Myeloma Working Group (IMWG) response criteria and the safety profile is described using NCI-CTCAE v5.0.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
33 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A study of carfilzomib, pomalidomide and dexamethasone administration after KRd administration
Arm Type
Experimental
Arm Description
Patients with RRMM who progressed after receiving lenalidomide monotherapy for at least 6 months after administration of KRd will receive KPD therapy every 4 weeks until disease progression.
Intervention Type
Drug
Intervention Name(s)
Carfilzomib 56 MG [Kyprolis]
Intervention Description
Carfilzomib 56 mg/m2 (Day1, 8, 15) (Cycle1 Day1, 20 mg/m2)
Intervention Type
Drug
Intervention Name(s)
Pomalidomide
Intervention Description
Pomalidomide 4 mg per os (Day1-21)
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
Dexamethasone 40 mg (D1, 8, 15, 22) (20 mg for patients ≥ 75 years old)
Primary Outcome Measure Information:
Title
Overall response rate
Description
percentage of patients who achieve at least partial response
Time Frame
assessed for approximately 3 years after administration
Secondary Outcome Measure Information:
Title
Complete response rate
Description
percentage of patients who achieve complete response
Time Frame
assessed for approximately 3 years after administration
Title
Progression free survival rate
Description
percentage of patients who are disease free or alive
Time Frame
assessed for approximately 3 years after administration
Title
Overall survival
Description
from the time of written consent to the time of death or last follow-up
Time Frame
assessed for approximately 3 years after administration
Title
Duration of response
Description
from the time of achieving at least partial response to the time of progressive disease
Time Frame
assessed for approximately 3 years after administration
Title
Time to response
Description
from the time of written consent to the time of achieving at least partial response
Time Frame
assessed for approximately 3 years after administration
Title
Incidence of treatment-emergent adverse events
Description
Safety profiles of carfilzomib, pomalidomide, and dexamethasone for myeloma patients who had relapsed or progressed
Time Frame
assessed for approximately 3 years after administration
Title
Minimal residual disease negativity
Description
The specimen is bone marrow aspirate, and it should be free of clonal plasma cells by examination by the NGF (next-generation flow) method. At this time, the test should be performed according to the EuroFlow standard operation procedure for MRD detection in MM, and the minimum sensitivity should be10 to the 5th power or higher.
Time Frame
up to 3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age from 20 to 80 years-old Relapse or progression of multiple myeloma after treatment of carfilzomib/lenalidomide/dexamethasone (KRd) KRd treatment 12 cycles or more and lenalidomide maintenance for at least 6 months or KRd 4-6 cycles followed by ASCT and lenalidomide maintenance for at least 6 months Measurable disease Serum M-protein ≥ 1 g/dL (10 g/L) Urine M-protein ≥ 200 mg/24 hr Serum FLC assay: difference of FLC ≥ 10 mg/dL (100 mg/L) provided serum FLC ratio is abnormal (KL ratio < 0.26 or > 1.65) if Serum EP or urine EP is not measurable Adequate organ functions Absolute Neutrophil Count (ANC) ≥ 1.0 x 109/L Platelets ≥ 50 x 109/L (≥ 30 x 109/L if myeloma involvement is > 50% in the bone marrow) Hemoglobin ≥ 8.0 g/dL Creatinine clearance ≥ 30 mL/minute or Serum Cr <3.0 g/dL Serum Bilirubin ≤ 1.5 x ULN AST and ALT ≤ 3 x ULN Eastern Cooperative Oncology Group performance scale 0~2 Life expectancy longer than 3 months Written informed consent Prior therapy with bortezomib Patients who meet the following criteria If a woman of childbearing age Women who are willing to use two reliable methods of contraception from 4 weeks prior to administration of study drug, while receiving, temporarily suspending administration, and 4 weeks after administration of the study drug. Women who have a negative pregnancy test with a minimum sensitivity of 25 IU/mL under medical management For men Men who agree to abstain from absolute abstinence or use a proper method of contraception for the entire duration of treatment and 28 days after the last dose Women of childbearing age Women who have not undergone hysterectomy or bilateral oophorectomy, women who have not undergone spontaneous menopause for at least 24 consecutive months (i.e., menstruate at any time during the last 24 months. However, amenorrhea after chemotherapy does not exclude the possibility of pregnancy). Proper method of contraception Very effective way Intrauterine device, hormone therapy (hormone implant, intrauterine system releasing levonorgestrel, medroxyprogesterone acetate depot injection, tablets containing progesterone to inhibit ovulation), tubal ligation, varicose veins in men Effective way Men's condom use, diaphragm method, cervical cap Exclusion Criteria: Grade 3~4 non-hematologic toxicity by carfilzomib during the previous carfilzomib treatment Prior therapy with pomalidomide Hypersensitivity to thalidomide or lenalidomide Previous refractoriness to carfilzomib according to the IMWG criteria Myocardial infarct within 6 months, heart failure of NYHA Class III~IV, uncontrolled ventricular arrhythmia, severe coronary arterial obstructive disease Active infection with 14 days prior to treatment Uncontrolled hypertension (Defined as an average systolic blood pressure >= 160 mmHg or diastolic >= 100 mmHg) or diabetes (HbA1c > 7.0%) HIV, HBV, HCV infection (exception if adequately controlled HBV (undetectable HBV DNA (< 20 IU/mL or concurrent use of an anti-viral agent), HCV) Severe or uncontrolled medical conditions, laboratory abnormalities, or psychiatric disorders that may preclude the participation of the study by the physician's discretion Contraindication to any of the required concomitant drugs or supportive treatments, including hypersensitivity to all anticoagulation and antiplatelet options, antiviral drugs, or intolerance to hydration due to preexisting pulmonary or cardiac impairment Diagnosis of other malignant disease other than myeloma within 5 year. Exceptions are properly treated non-melanomatous skin cancers, cervical intraepithelial neoplasia, prostate cancer that do not require treatment, or properly excised well-differentiated thyroid cancers. Pregnant or nursing women Waldenstroem's macroglobulinemia, POEMS syndrome, or plasma cell leukemia, light chain amyloidosis LV ejection fraction < 40%
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kihyun Kim, Ph.D
Phone
82-2-2148-7333
Email
kihyunk.kim@samsung.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kihyun Kim, Ph.D
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bobae Lee
Phone
82-2-2148-7690
Email
bb.lee@sbri.co.kr
First Name & Middle Initial & Last Name & Degree
Kihyun Kim, Ph.D

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Phase II Study of Carfilzomib, Pomalidomide, and Dexamethasone for Myeloma Patients Who Had Relapsed or Progressed After Carfilzomib, Lenalidomide, and Dexamethasone

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