Session: 654. Multiple Myeloma: Pharmacologic Therapies: Poster I
Hematology Disease Topics & Pathways:
Research, Clinical trials, Combination therapy, Clinical Research, Treatment Considerations
Methods: The SPd arm of the multi-arm STOMP study evaluated selinexor at multiple doses and schedules in combination with Pd (P doses tested consisted of 2 mg, 3 mg, or 4 mg QD) in patients with RRMM. Study objectives were to determine the maximum tolerated dose and the recommended Phase 2 dose to assess safety and to examine the efficacy of the SPd regimen. Response assessments were investigator-determined per International Myeloma Working Group criteria.
Results:
Patient Demographics
As of March 25, 2024, 81 patients had been enrolled in the SPd arm, including 20 in the 60 mg QW (SPd60) and 16 in the 40 mg QW (SPd40) groups. Of all patients treated with SPd, 53.1% were male, the median age was 65, and patients had a median 3 prior lines of therapy. Percentage of patients with prior exposure/refractory status to IMiD was 100%/86.4%; PI 100%/80.2%, αCD38 33.3%/30.9%, and TCE: 33.3%/25.9%.
Efficacy
The investigator-assessed overall response rate (ORR) was 39.5% (95% CI 28.8, 51.0) for the entire cohort, 55.0% (95% CI 31.5, 76.9) for SPd60, and 43.8% (95% CI 19.8, 70.1) for SPd40. The very good partial response or better rate was 19.8% (95% CI 11.7, 30.1) in the entire cohort, 30.0% (95% CI 11.9, 54.3) in SPd60, and 31.3% (95% CI 11.0, 58.7) in SPd40. There were 2 stringent complete responses (CRs; 1 in SPd60 and 1 in SPd40, both TCE) and 1 CR (SPd40). For the entire cohort, the median time to response was 1.1 months (95% CI 1.0, 2.0).
Updated PFS and duration of response results will be presented.
Safety
The most common treatment emergent adverse events (TEAEs) were:
Neutropenia
- Entire cohort: 67.9% any grade/60.5% G3-4
- SPd60: 75.0%/60.0%
- SPd40: 68.8%/68.8%
Fatigue
- Entire cohort: 64.2%/13.6%
- SPd60: 75.0%/15.0%
- SPd40: 62.5%/6.3%
Nausea
- Entire cohort: 61.7%/1.2%
- SPd60: 70.0%/0
- SPd40: 50.0%/0
Anemia
- Entire cohort: 54.3%/33.3%
- SPd60: 65.0%/25.0%
- SPd40: 31.3%/18.8%
Thrombocytopenia
- Entire cohort: 49.4%/29.6%
- SPd60: 45.0%/25.0%
- SPd40: 25.0%/18.8%
Median duration of exposure in weeks was 19.0 (range 1, 260) in the entire cohort, 22.0 (7, 114) in SPd60, and 28.0 (4, 176) in SPd40. Median relative selinexor dose intensity was 86.4% (57.5 mg/week) for the entire cohort, 77.5% (46.5 mg/week) for SPd60, and 93.2% (37.3 mg/week) for SPd40.
Conclusions: The all-oral combination of SPd showed signs of preliminary efficacy and was generally tolerable in patients with RRMM. Although the ORR was greater in the SPd60 cohort, TEAEs were less frequent, duration of exposure was longer, and higher dose intensity was achieved for patients treated with SPd40. These data support the further evaluation of low-dose weekly selinexor in the ongoing EMN29 trial (NCT05028348) of SPd40 versus elotuzumab and Pd in TCE RRMM progressing immediately after a αCD38-containing line of therapy.
Disclosures: Baljevic: Janssen Biotech, BMS/Celgene, Sanofi-Genzyme: Other: advisory board; AbbVie, Pfizer: Consultancy; Parexel: Other: IRC. Bahlis: Pfizer, Janssen: Research Funding; AbbVie, Amgen, BMS, Celgene, Janssen, GSK, Genentech, Karyopharm, Kyte, Novartis, Pfizer, Roche, Sanofi, Takeda: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees. Kotb: Karyopharm.: Current holder of stock options in a privately-held company; Akcea, Amgen, Bristol Myers Squibb, Celgene, Janssen, Merck, Pfizer, Sanofi, Takeda: Honoraria; Merck, Sanofi: Research Funding. Lipe: Janssen and amgen: Research Funding; Janssen, karyopharm, bms, Sanofi, Pfizer, and abbvie: Consultancy, Honoraria. Madan: Harpoon, Karyopharm: Other: Travel, accommodations, expenses; Karyopharm, Sanofi, Pfizer, Janssen: Consultancy; Karyopharm, Harpoon, Pfizer, Iteos: Research Funding. Sutherland: Sanofi: Consultancy; Celgene: Consultancy; Amgen: Consultancy; GSK: Research Funding; Karyopharm: Research Funding; Janssen: Consultancy, Research Funding. Lentzsch: Caelum Bioscience: Patents & Royalties; Pfizer, Regeneron, Janssen, GSK, Sanofi, BMS, Karyopharm, Antigia: Consultancy, Membership on an entity's Board of Directors or advisory committees; PeerView, Clinical Care, Options (CCO), RedMed, Aptitude, Bio Ascend: Speakers Bureau. Biran: Amgen: Research Funding; AbbVie: Consultancy; Karyopharm: Research Funding; Bristol Myers Squibb: Consultancy, Honoraria, Research Funding, Speakers Bureau; Janssen: Consultancy, Honoraria, Research Funding, Speakers Bureau; Sanofi: Honoraria, Speakers Bureau; Pfizer: Consultancy, Honoraria. Van Domelen: Karyopharm Therapeutics: Current Employment. Mark: Karyopharm Therapeutics: Current Employment. White: GSK: Honoraria; Pfizer: Honoraria; Sanofi: Honoraria; Karyopharm: Honoraria; Janssen: Honoraria; Forus: Honoraria; BMS: Honoraria; Antengene: Honoraria; Amgen: Honoraria.
OffLabel Disclosure: Selinexor approved in combination with dexamethasone (d) in penta-refractory MM and with d + bortezomib in relapsing/refractory MM (RRMM) after ≥1 prior therapy
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