Once-Weekly Carfilzomib, Lenalidomide, Dexamethasone, and Isatuximab in Newly Diagnosed, Transplant-Eligible Multiple Myeloma: The SKylaRk Trial

2022 Year in Review - Multiple Myeloma

A phase 2 study of isatuximab added to weekly carfilzomib, lenalidomide, and dexamethasone demonstrated promising efficacy and safety in transplant-eligible patients with newly diagnosed multiple myeloma.

Isatuximab is a novel CD38 monoclonal antibody being studied in a variety of novel combination strategies. SKylaRk is a phase 2 trial evaluating the addition of isatuximab to weekly carfilzomib, lenalidomide, and dexamethasone (Isa-KRd) in all-risk, transplant-eligible patients with newly diagnosed multiple myeloma. Elizabeth K. O’Donnell presented results from this phase 2 trial at the 2022 American Society of Hematology meeting.

A total of 50 eligible patients received 4 cycles of induction therapy with Isa-KRd followed by investigator’s choice of upfront versus deferred stem-cell transplant (SCT). Patients undergoing SCT received 2 additional cycles of therapy and then maintenance therapy, and patients deferring SCT received an additional 4 cycles of therapy and then maintenance therapy. Patients were stratified by cytogenetics for maintenance therapy; patients with standard-risk cytogenetics received lenalidomide, and patients with high-risk cytogenetics received isatuximab, carfilzomib, and lenalidomide. Twenty-three patients had high-risk cytogenetics (including deletion 17p, gain of 1q, and translocations t[4:14], t[14;16], and t[14;20]). Forty-seven patients were evaluable for response after 4 cycles, and the overall response rate (ORR) was 94%; 84% achieved a very good partial response (VGPR) or better and 38% achieved a complete response (CR). Minimal residual disease (MRD) results were available for 28 patients after 4 cycles who achieved a VGPR or better, and 43% were MRD negative at 105. After 8 cycles of therapy, ORR was 100%, 95% of patients achieved a VGPR or better, 67% achieved a CR, and 74% of evaluable patients achieved MRD negativity. Five patients elected to go with upfront transplant, and the ORR was 100%. The 15-month progression-free survival was 88.6%, and the 15-month overall survival was 98%. The most common grade 3 or 4 adverse events were neutropenia (28%), elevated alanine aminotransferase (14%), anemia (10%), hypertension (8%), thrombocytopenia (6%), acute kidney injury (6%), and fatigue (6%).

These data showed promising results with Isa-KRd, with an ORR of 100% and predictable safety profile.

Reference

  1. O’Donnell EK, Mo CC, Nadeem O, et al. A phase II study of once weekly carfilzomib, lenalidomide, dexamethasone, and isatuximab in newly diagnosed, transplant-eligible multiple myeloma (The SKylaRk Trial). Presented at: 2022 American Society of Hematology Annual Meeting; December 10-13; New Orleans, LA. Abstract 3239.

Related Items

Updates to NCCN Guidelines for Multiple Myeloma: Recently Approved First-Line Treatments for Patients With NDMM Eligible and Ineligible for Transplant
Web Exclusives
Two quadruplet therapies have been approved by the FDA as first-line treatment for patients with newly diagnosed multiple myeloma (NDMM) and updated in the NCCN guidelines for the treatment of multiple myeloma.
Teclistamab Showed Durable Responses in Heavily Pretreated Patients with Multiple Myeloma
2022 Year in Review - Multiple Myeloma
Phase 2 results from MajesTEC-1 showed substantial clinical activity with teclistamab and are consistent with phase 1 findings.
GC012F, an Autologous BCMA and CD19 Dual-Targeting CAR T-Cell Therapy, as First-Line Treatment for Transplant-Eligible Patients with Newly Diagnosed High-Risk Multiple Myeloma
2022 Year in Review - Multiple Myeloma
A phase 1 trial of GC012F demonstrated an overall response rate of 100% in high-risk, transplant-eligible patients with newly diagnosed multiple myeloma.
Journal of Oncology Navigation & Survivorship
JONS

Subscribe Today!

To sign up for our print publication or e-newsletter, please enter your contact information below.

I'd like to receive:

  • First Name *
    Last Name *
     
    Profession or Role
    Primary Specialty or Disease State
    Country