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1025 Mezigdomide (MEZI) Plus Dexamethasone (DEX) and Bortezomib (BORT) or Carfilzomib (CFZ) in Patients (pts) with Relapsed/Refractory Multiple Myeloma (RRMM): Updated Results from the CC-92480-MM-002 Trial

Program: Oral and Poster Abstracts
Type: Oral
Session: 654. Multiple Myeloma: Pharmacologic Therapies: Into the Future: New Drugs and Combinations in Multiple Myeloma
Hematology Disease Topics & Pathways:
Clinical trials, Research, Combination therapy, Clinical Research, Plasma Cell Disorders, Diseases, Treatment Considerations, Biological therapies, Immunotherapy, Lymphoid Malignancies
Monday, December 9, 2024: 5:30 PM

Irwindeep Sandhu, MD1*, Paul G. Richardson2, Albert Oriol3*, Darrell White4, Richard Leblanc, MD, FRCPC5, Noopur Raje6, Enrique M. Ocio7, Aurore Perrot, MD, PhD8, Thierry Facon9*, Cesar Rodriguez, MD10*, Ralph Wäsch11, Meletios A. Dimopoulos, MD12, Tracy T. Chow13*, Allison Gaudy13*, Jing Gong13*, Zehua Zhou13*, Tiziana Civardi14*, Joseph T. Hadala13*, Yue Zhu13*, Jessica Katz13 and Marc S. Raab15*

1University of Alberta, Edmonton, AB, Canada
2Dana-Farber Cancer Institute, Boston, MA
3Catalan Institute of Oncology and Josep Carreras Institute, Hospital Germans Trias i Pujol, Badalona, Spain
4Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada
5Hôpital Maisonneuve-Rosemont, Université de Montréal, Montreal, Canada
6Massachusetts General Hospital, Boston, MA
7Hospital Universitario Marqués de Valdecilla (IDIVAL), Universidad de Cantabria, Santander, Spain
8Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France
9Centre Hospitalier Universitaire (CHU) Lille, Service des Maladies du Sang, University of Lille, Lille, France
10Department of Medicine, Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY
11Department of Medicine, University of Freiburg Medical Center, Freiburg, Germany
12National and Kapodistrian University of Athens, Athens, Greece
13Bristol Myers Squibb, Princeton, NJ
14Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland
15Heidelberg Myeloma Center, Department of Medicine V, University Hospital Heidelberg, Heidelberg, Germany

Introduction: MEZI is a novel, potent, oral CELMoD™ agent with enhanced tumoricidal and immune-stimulatory effects compared with immunomodulatory drugs (IMiDs®). Preclinically, MEZI has shown marked synergy with DEX and other antimyeloma therapies, including proteasome inhibitors (PIs). In the phase 1/2 CC-92480-MM-002 trial (NCT03989414), MEZI combined with DEX and BORT (MeziVd) or DEX and CFZ (MeziKd) showed meaningful clinical activity and manageable tolerability in pts with RRMM. Here we report updated results with longer follow-up from the MeziVd and MeziKd dose-escalation cohorts (A and C) and the MeziVd dose-expansion cohort (D).

Methods: Eligible pts had RRMM, 2–4 (Cohorts A and C) or 1–3 (Cohort D) prior regimens including lenalidomide, and documented progressive disease (PD) during or after the last myeloma therapy. Oral MEZI was given at escalating doses of 0.3, 0.6, or 1.0 mg (Cohort A) or at 0.6 or 1.0 mg (Cohort D) on days (D)1–14 of each 21-D cycle with BORT + DEX, or at escalating doses (0.3, 0.6, or 1.0 mg) on D1–21 of each 28-D cycle with CFZ + DEX (Cohort C). Pharmacokinetics samples were collected on D1 and D8 of cycle (C)1 and D8 of C2–8, and also on C1D11 for Cohorts A and D. Biomarker analyses included peripheral blood samples collected on C1D1 to mid-C3 for substrate degradation and immunomodulation by flow cytometry. The primary objectives were to determine the recommended dose and regimen (dose-escalation cohorts) and evaluate safety and efficacy.

Results: As of May 9, 2024, 104 pts were enrolled in Cohorts A, C, and D; 28 pts received MeziVd (Cohort A) and 27 pts received MeziKd (Cohort C) in the dose-escalation cohorts. Median (range) age was 65.5 (46–86) and 68 (41–76) years (y), median time since diagnosis was 4.8 (1.9–17.1) and 5.4 (0.7–15.7) y, median number of prior regimens was 3 (2–4) and 2 (2–4), 24 (85.7%) and 24 (88.9%) pts were refractory to IMiD agents, and 14 (50.0%) and 14 (51.9%) to PIs, respectively. Median follow-up was 13.6 (MeziVd) and 15.2 months (mo) (MeziKd); 3 (10.7%) and 5 (18.5%) pts continue on treatment, with 12.5 and 12 median cycles received, and PD being the main reason for discontinuation (64.3% and 48.1%), respectively.

In the dose-escalation cohorts, the most common grade 3/4 treatment-emergent adverse events (TEAEs) were neutropenia (35.7%), thrombocytopenia (21.4%), and infections (17.9%) with MeziVd; and neutropenia (44.4%) and infections (33.3%) with MeziKd. Grade 3/4 non-hematologic TEAEs, including rash and diarrhea, were low or absent. MEZI dose reductions due to TEAEs were needed in 7 (25.0%) and 8 (29.6%) pts. The overall response rate (ORR) was 75.0% (21/28 pts) and 85.2% (23/27 pts), with ≥ very good partial responses (VGPR) in 39.3% and 44.4% pts. Median (95% CI) duration of response (DOR) was 10.9 (8.1–18.7) and 11.9 (6.4–NA) mo and median (95% CI) progression-free survival (PFS) was 11.8 (9.0–18.0) and 13.5 (8.4–19.7) mo, respectively.

As of May 9, 2024, 49 pts received MeziVd in the Cohort D dose-expansion cohort. Median age was 64 (43–83) y, median time since diagnosis was 4.2 (0.9–20.5) y, and median number of prior regimens was 1 (1–3). Overall, 31 (63.3%) pts were refractory to IMiD agents, and 8 (16.3%) to PIs. Median follow-up was 18.3 mo; 9 (18.4%) pts continue on treatment, with 15 median cycles received. Discontinuations were mainly due to PD (53.1%).

The most common grade 3/4 TEAEs were neutropenia (63.3%), infections (32.7%), and thrombocytopenia (26.5%); grade 3/4 non-hematologic TEAEs remained low or absent. MEZI dose reductions due to TEAEs were needed in 18 (36.7%) pts. ORR was 85.7% (42/49 pts) with ≥ VGPR in 63.3% of pts; median DOR was 19.4 (9.7–NA) mo, median PFS was 17.5 (9.4–24.0) mo.

MEZI exposure increased in a dose-linear manner over the dose range, and exposures were similar when comparing pts treated with MeziVd and MeziKd. MEZI showed pharmacodynamic activity with BORT or CFZ across all doses tested, with 1.0 mg MEZI inducing the greatest pharmacodynamic effects including substrate degradation and T-cell proliferation, supporting the use of 1.0 mg MEZI in combination with PIs.

Conclusions: With longer follow-up, MeziVd and MeziKd in RRMM confirmed promising efficacy and a manageable safety profile at all dose levels tested, with no cumulative toxicity and low grade 3/4 non-hematologic TEAEs (including rash and diarrhea). These results informed ongoing and planned phase 3 trials. Updated data will be presented at the meeting.

Disclosures: Sandhu: Bristol-Myers Squibb - Celgene: Consultancy, Honoraria; Sanofi: Consultancy, Honoraria; Johnson & Johnson - Janssen: Consultancy, Honoraria; GSK: Consultancy, Honoraria; Pfizer: Consultancy, Honoraria. Richardson: Oncopeptides: Research Funding; Celgene/Bristol Myers Squibb, GSK, Karyopharm Therapeutics, Oncopeptides, Regeneron, Sanofi: Consultancy. Oriol: GSK: Honoraria, Speakers Bureau; Pfizer, Amgen, Oncopeptides: Honoraria; Bristol Myers Squibb/Celgene: Honoraria, Speakers Bureau; Sanofi: Honoraria, Speakers Bureau; Johnson & Johnson, Janssen: Honoraria, Speakers Bureau. White: Apobiologix: Honoraria; Pfizer: Honoraria; Amgen: Honoraria; Karyopharm: Honoraria; Antengene: Honoraria; BMS: Honoraria; Sanofi: Honoraria; GSK: Honoraria; Forus: Honoraria. Leblanc: FORUS Therapeutics: Membership on an entity's Board of Directors or advisory committees; Sanofi: Membership on an entity's Board of Directors or advisory committees, Research Funding; Amgen: Membership on an entity's Board of Directors or advisory committees, Research Funding; Pfizer: Honoraria, Membership on an entity's Board of Directors or advisory committees; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees; Bristol Myers Squibb: Membership on an entity's Board of Directors or advisory committees. Raje: bluebird bio: Membership on an entity's Board of Directors or advisory committees, Research Funding; Janssen Biotech Inc: Membership on an entity's Board of Directors or advisory committees; Onyx Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees; Roche Laboratories Inc: Other: Steering Committee; Celgene Corporation: Membership on an entity's Board of Directors or advisory committees; Amgen Inc: Other: Steering Committee; Bristol-Myers Squibb: Membership on an entity's Board of Directors or advisory committees; Immuneel Therapeutics: Membership on an entity's Board of Directors or advisory committees; Takeda Pharmaceuticals USA Inc: Membership on an entity's Board of Directors or advisory committees; Merck: Membership on an entity's Board of Directors or advisory committees; Novartis: Membership on an entity's Board of Directors or advisory committees; Caribou Biosciences Inc: Membership on an entity's Board of Directors or advisory committees. Ocio: AstraZeneca: Consultancy; Menarini: Consultancy, Honoraria; Janssen: Consultancy, Honoraria, Speakers Bureau; Takeda: Consultancy, Honoraria; AbbVie: Consultancy, Honoraria; Pfizer: Consultancy, Honoraria; Oncopeptides: Consultancy, Honoraria, Research Funding; GSK: Consultancy, Honoraria, Research Funding; Amgen: Honoraria; Bristol Myers Squibb: Consultancy, Honoraria; Regeneron: Honoraria; Sanofi: Consultancy, Honoraria. Perrot: Takeda: Honoraria, Research Funding; Pfizer: Honoraria, Membership on an entity's Board of Directors or advisory committees; Amgen: Honoraria; GSK: Honoraria; Abbvie: Honoraria; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees; Sanofi: Honoraria, Research Funding; BMS: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Menarini Stemline: Honoraria. Rodriguez: Takeda: Consultancy; Sanofi: Consultancy; Johnson and Johnson: Consultancy; Janssen: Consultancy; BMS: Consultancy; Amgen: Consultancy; AbbVie: Consultancy; Karyopharm Therapeutics: Consultancy. Wäsch: Janssen, Sanofi: Research Funding; Amgen,BMS/Celgene, Janssen, Kite/Gilead, Novartis, Pfier, Sanofi: Consultancy; Abbvie,Amgen, BMS/Celgene, Janssen, Kite/Gilead, Pfizer, Sanofi: Honoraria. Dimopoulos: Regeneron: Honoraria, Membership on an entity's Board of Directors or advisory committees; Menarini: Honoraria, Membership on an entity's Board of Directors or advisory committees; Takeda: Honoraria, Membership on an entity's Board of Directors or advisory committees; GlaxoSmithKline: Honoraria, Membership on an entity's Board of Directors or advisory committees; Bristol Myers Squibb: Honoraria, Membership on an entity's Board of Directors or advisory committees; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees; BeiGene: Honoraria, Membership on an entity's Board of Directors or advisory committees; Swixx: Honoraria, Membership on an entity's Board of Directors or advisory committees; AstraZeneca: Honoraria, Membership on an entity's Board of Directors or advisory committees; Sanofi: Honoraria, Membership on an entity's Board of Directors or advisory committees; Amgen: Honoraria, Membership on an entity's Board of Directors or advisory committees. Chow: BMS: Current Employment, Current equity holder in publicly-traded company. Gaudy: BMS: Current Employment, Current equity holder in publicly-traded company. Gong: Bristol Myers Squibb: Current Employment. Zhou: BMS: Current Employment, Current equity holder in publicly-traded company. Civardi: BMS: Current Employment, Current equity holder in publicly-traded company. Hadala: Bristol Myers Squibb: Current Employment, Current holder of stock options in a privately-held company. Zhu: Bristol Myers Squibb: Current Employment. Katz: Bristol Myers Squibb: Current Employment, Current equity holder in publicly-traded company. Raab: Pfizer: Consultancy, Membership on an entity's Board of Directors or advisory committees; BMS: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: travel expenses, Research Funding; Amgen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: travel expenses; Sanofi: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Heidelberg Pharma: Research Funding; Takeda: Consultancy, Membership on an entity's Board of Directors or advisory committees; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: travel expenses, Research Funding; Abbvie: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Oncopeptides: Consultancy, Honoraria, Other: travel expenses; GSK: Consultancy, Membership on an entity's Board of Directors or advisory committees.

*signifies non-member of ASH