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NCT Number: NCT02217163

Carfilzomib, Cyclophosphamide, Dexamethasone in Transplant Eligible Newly Diagnosed High-risk Multiple Myeloma

Patients with high risk multiple myeloma have shorter remission periods and reduced overall survival. Prognostic significance of minimal residual disease negative remission is being highlighted in many of the newer studies.

The current phase 2 study investigates the combination of carfilzomib together with cyclophosphamide and dexamethasone in patients with high risk multiple myeloma in younger transplant-eligible patients.

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Key information

Age range

21 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

National University Hospital, Singapore

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About this study

Carfilzomib is administered over 30 minutes as an infusion. For cycle 1 only, Carfilzomib is administered at 20mg/m2 IV on days 1 and 2, followed by escalation to 36 mg/m2 on days 8,9,15 and 16 on a 28 day cycle. Patients who tolerate 36 mg/m2 dose are kept at this dose for the subsequent cycles on Days 1, 2, 8, 9, 15, 16 on a 28 day cycle. Dose and schedule modifications for intolerable side effects are detailed in the protocol. Additionally Cyclophosphamide is given a fixed dose of 500mg once per week orally, along with dexamethasone, given on the days of Carfilzomib administration, 30 minutes to 4 hours prior to Carfilzomib. Patients will undergo blood tests weekly and serum protein electrophoresis every 4 weeks during treatment. Within completion of 5 cycles of treatment, patients would undergo stem cell collection using chemotherapy and GCSF mobilization. After completion of 6 cycles of treatment, autologous bone marrow transplantation will be performed. Three months following bone marrow transplantation, subjects will undergo further 2 consolidation cycles. After consolidation, subjects will undergo disease assessment by blood and subjects who are in CR will undergo bone marrow investigations and MRD analysis MPFC. Patients who achieve MRD negativity by MPFC will be managed expectantly by watch and wait. Patients who are MRD positive at this stage will receive maintenance for 2 years or till disease progression. Follow up would extend till a minimum of 2 years from completion of the study. At the end of 2 years post maintenance or expectant monitoring, subjects who are in CR will undergo disease assessment by blood and bone marrow investigations and MRD analysis MPFC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Newly diagnosed Multiple Myeloma AND Transplant eligible AND
  • High Risk as defined by:
  • International Staging System 3 OR
  • FISH abnormality of t(4,14), t(14;16), 17p deletion or 1q amp
  • Patients must have evaluable myeloma, with at least one of the following (Assessed within 28 days of commencing the study)
  • Serum M protein >/= 0.5g/dL or
  • Urine M protein >200mg/24hr
  • Serum free light chains >100mg/mL (involved light chain) and abnormal k/l ratio
  • For IgA patients who have no other means of measurement of disease, sIgA level >0.75g/dL

Exclusion criteria

  • Relapsed Myeloma
  • Non transplant eligible patient.
  • IgM subtype Myeloma
  • POEMS syndrome
  • Amyloidosis
  • Waldenstroms Macroglobulinemia
  • Radiation therapy to an extended field involving a significant volume of bone marrow within 21 days of randomization (Limited site radiation allowed).

Treatment and study plan

Carfilzomib, , Cyclophosphamide, Dexamethasone

Drug

Carfilzomib is administered intraveneously over 30 minutes. For cycle 1 only, Carfilzomib is administered at 20mg/m2 on Day 1 and 2, dose will be escalated to 36mg/m2 on Day 8,9,15 and 16 of the 28-days cycle. Patients who tolerate the 36mg/m2 dose are kept at this dose for the subsequent cycles on Day 1,2,8,9,15,16 on a 28 days cycle. Cyclophosphamide is given at a fixed dose of 500mg once per week orally, along with dexamethasone which is given on the days of Carfilzomib administration, 30 minutes to 4 hours prior to Carfilzomib infusion.

Other names: Kyprolis

Primary outcomes

  1. Progression Free Survival

    Time frame: 2 years

    To study the progression free survival (PFS) in patients with newly diagnosed high risk multiple myeloma treated with Carfilzomib, Cyclophosphamide and Dexamethasone, followed by autologous bone marrow transplantation.

Secondary outcomes

  1. Minimal residual disease negativity

    Time frame: 2 years

    Minimal residual disease burden at different time points, as assessed by multi parameter flow cytometry (MPFC).

  2. Overall Survival (OS)

    Time frame: 2 years

    OS is defined as the time from entering study to death of any cause.

Sponsors and collaborators

Lead sponsor

Singapore General Hospital

Other

Registry information

Official study title

Study of Carfilzomib in Transplant Eligible Newly Diagnosed High-risk Multiple Myeloma

Important dates

Study start
2014
Primary completion
2020
Study completion
2020
First posted
Aug 15, 2014
Registry last updated
Oct 20, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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