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3386 Prommis Trial Prospectively Demonstrates the Efficacy of SKY92 Risk Stratification in Newly Diagnosed Multiple Myeloma PatientsClinically Relevant Abstract

Program: Oral and Poster Abstracts
Session: 653. Multiple Myeloma: Prospective Therapeutic Trials: Poster II
Hematology Disease Topics & Pathways:
Research, clinical trials, Clinical Research, real-world evidence, Technology and Procedures, molecular testing
Sunday, December 10, 2023, 6:00 PM-8:00 PM

Noa Biran1*, Binod Dhakal, MBBS2, Ruben Niesvizky, MD3, Suzanne Lentzsch, MD, PhD4, John T. McKay5*, David H. Vesole, MD, PhD6,7, Ajay K. Nooka, MD, MPH8, Barry Paul, MD, MS9, Parameswaran N. Hari, MD, MBBS10, Lisette Stork-Sloots11*, Silvia D'Ambrosi12*, Rowan Kuiper12*, Martin van Vliet12*, David S. Siegel, MD, PhD1, Saad Z Usmani, MD13 and Frits van Rhee, MD, PhD14

1Hackensack University Medical Center, Hackensack, NJ
2BMT and Cellular Therapy Program, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI
3Division of Hematology & Medical Oncology, Weill Cornell Medicine/New York Presbyterian Hospital, New York, NY
4Division of Hematology & Oncology, Columbia University Medical Center, New York, NY
5Wake Forest University School of Medicine, Winston-Salem, NC
6Lombardi Comprehensive Cancer Center, Medstar Georgetown Medical Center, Washington, DC, DC
7Multiple Myeloma Division, John Theurer Cancer Center, Hackensack Meridian Health, Hackensack, NJ
8Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA
9Department of Hematologic Oncology & Blood Disorders, Atrium Health Levine Cancer Institute, Charlotte, NC
10Department of Medicine, Medical College of Wisconsin, Milwaukee
11Medex15, Amsterdam, Netherlands
12SkylineDx, Rotterdam, Netherlands
13Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY
14Myeloma Center, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR

Introduction: Multiple myeloma (MM) is a complex hematologic malignancy characterized by genetic instability, variable survival rates, and diverse treatment responses. SKY92 gene expression profiling (GEP) is a valuable tool in risk stratifying patients into high-risk and standard-risk groups for progression and survival. The PRospective Observational Multiple Myeloma Impact Study (PROMMIS; NCT02911571) trial, a prospective US multicenter study, was designed to validate the prognostic performance of SKY92 through real-world data.

Methods: The GEP of 251 newly diagnosed MM patients was assessed using the SKY92 assay (SkylineDx, San Diego), which involved analyzing RNA extracted from CD138-positive plasma cells (≥80% purity) isolated through immunomagnetic separation. The test was performed at the enrolling institute, or by sending the samples into a central lab. The standard method for risk stratification by R-ISS stage was integrated with SKY92 into three distinct groups: Low-Risk (LR), defined by SKY92 standard-risk (SR) combined with R-ISS I; Intermediate Risk (IR), as SKY92 SR with R-ISS II/III, or SKY92 high-risk with R-ISS I; and High-Risk as SKY92 high-risk with R-ISS II/III. Progression-free survival (PFS) and overall survival (OS) were available for 221 patients, measured from the date of diagnosis of the patients. The median follow-up at the time of analysis is 38 months. Survival analyses were performed using Cox proportional hazards model.

Results: Upon analysis, 179 patients (71.3%) were classified as SKY92 standard-risk, and 72 patients (28.7%) as SKY92 high-risk. Notably, the percentage of high-risk patients in this study was slightly higher than that observed in previous retrospective analyses (15-25%).

Furthermore, the survival analysis revealed significant differences in both PFS (HR: 2.1, 95%CI 1.4-3.1, p<0.001) and OS (HR: 3.7, 95%CI 1.8-7.6, p<0.001) between the two risk categories. The median PFS from the time of the diagnosis for SKY92 standard-risk patients was 50 months, whereas for SKY92 high-risk patients, it was 26 months. The median OS was not reached within the 60-month timeframe for both the standard- and high-risk groups.

R-ISS could be determined for 204 patients (81%), of which 29.9% (n=61) were classified as stage I, 59.3% (n=121) as stage II, and 10.8% (n=22) as stage III. We integrated R-ISS staging with SKY92 classification for these patients. The combination of these two classification systems yielded the following stratification (Figure 1): LR n=53 (27%), IR n=96 (47%), and High-Risk n=55 (26%). Consistent with previous studies, R-ISS and SKY92 hold independent prognostic value: in particular, we found that this combined classification method identified a higher number of patients as high-risk compared to the R-ISS annotation (55 [27%] vs. 22 [11%]). The high-risk group exhibited significantly shorter OS and PFS compared to the LR group (OS: HR:18.7, 95% CI 2.5-140, p=0.004 and PFS: HR:2.6, 95% CI 1.4-4.7, p=0.002).

Conclusions: This study represents the first US-based multicenter prospective evaluation of the GEP SKY92 in a real-world clinical setting. The results obtained align with the retrospective validations of SKY92, further confirming its reliability as a prognostic marker for MM patients. In addition, we observed that the SKY92 is able to identify a higher number of high-risk patients, with significantly shorter PFS and OS, compared to the conventional R-ISS staging system.

Figure 1: PFS and OS based on SKY92+R-ISS risk classification

Disclosures: Biran: Janssen: Honoraria, 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; Karyopharm: Membership on an entity's Board of Directors or advisory committees, Research Funding; BMS: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Merck: Research Funding; Sanofi: Consultancy, 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; abbvie: Honoraria; Genomic testing cooperative: Divested equity in a private or publicly-traded company in the past 24 months; GSK: Membership on an entity's Board of Directors or advisory committees; Pfizer: Membership on an entity's Board of Directors or advisory committees; Boehringer Ingelheim: Other: spouse of employee. Dhakal: Janssen, Karyopharm, GSK, Arcellx, GSK, Sanofi, Genentech, Pfizer: Consultancy, Honoraria, Speakers Bureau. Niesvizky: BMS/Celgene: Consultancy, Research Funding; Takeda: Consultancy, Honoraria, Research Funding; Janssen: Consultancy, Honoraria, Research Funding; GSK: Consultancy, Honoraria, Research Funding; Karyopharm: Consultancy, Honoraria, Research Funding; Pfizer: Consultancy, Honoraria, Research Funding; Sanofi: Consultancy, Honoraria; Regeneron: Consultancy, Honoraria, Research Funding. Lentzsch: Janssen: Membership on an entity's Board of Directors or advisory committees; Caelum Biosciences: Membership on an entity's Board of Directors or advisory committees, Patents & Royalties: January 1, 2041; Alexion Pharmaceuticals: Consultancy, Membership on an entity's Board of Directors or advisory committees; Celgene: Research Funding; Bristol Meyers Squibb: Membership on an entity's Board of Directors or advisory committees; Regeneron: Honoraria; Pfizer: Consultancy; Oncopeptide: Membership on an entity's Board of Directors or advisory committees; Karyopharm Therapeutics: Membership on an entity's Board of Directors or advisory committees; Adaptive Biotechnologies: Consultancy, Membership on an entity's Board of Directors or advisory committees; Sanofi: Research Funding; Clinical Care Options: Honoraria; Takeda: Membership on an entity's Board of Directors or advisory committees. McKay: BMS: Consultancy. Nooka: Aduro Biotech, Amgen, Arch Oncology, Bristol Myers Squibb, Cellectis, Genentech, GlaxoSmithKline, Janssen, Karyopharm, Kite Pharma, Merck, Pfizer, Takeda: Honoraria, Research Funding; Adaptive Biotechnologies, Amgen, BeyondSpring, Bristol Myers Squibb, Cellectar Biosciences, GlaxoSmithKline, Janssen, Karyopharm, Oncopeptides, ONK therapeutics, Pfizer, Sanofi, Secura Bio, Takeda: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees. Paul: Janssen: Membership on an entity's Board of Directors or advisory committees. D'Ambrosi: SkylineDx: Current Employment. Kuiper: SkylineDx: Current Employment. van Vliet: SkylineDx: Current Employment. Siegel: Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Takeda: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Amgen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Celularity Scientific: Consultancy, Membership on an entity's Board of Directors or advisory committees; Celgene: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Novartis: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; BMS: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Karyopharm: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau. Usmani: GSK: Membership on an entity's Board of Directors or advisory committees, Research Funding; Novartis: Membership on an entity's Board of Directors or advisory committees; Moderna: Membership on an entity's Board of Directors or advisory committees; Janssen: Membership on an entity's Board of Directors or advisory committees, Research Funding; Sanofi: Membership on an entity's Board of Directors or advisory committees, Research Funding; Oncopeptides: Membership on an entity's Board of Directors or advisory committees; K36 Therapeutics: Membership on an entity's Board of Directors or advisory committees; SecuraBio: Membership on an entity's Board of Directors or advisory committees; Seattle Genetics: Membership on an entity's Board of Directors or advisory committees, Research Funding; SkylineDX: Membership on an entity's Board of Directors or advisory committees, Research Funding; Takeda: Membership on an entity's Board of Directors or advisory committees, Research Funding; Gilead Sciences: Membership on an entity's Board of Directors or advisory committees, Research Funding; Genentech: Membership on an entity's Board of Directors or advisory committees; EdoPharma: Membership on an entity's Board of Directors or advisory committees; TeneoBio: Membership on an entity's Board of Directors or advisory committees; Array Biopharma: Research Funding; Merck: Research Funding; Pharmacyclics: Research Funding; Celgene: Membership on an entity's Board of Directors or advisory committees, Research Funding; Bristol Meyer Squibb: 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; Abbvie: Membership on an entity's Board of Directors or advisory committees, Research Funding. van Rhee: Janssen Pharmaceuticals: Research Funding; Bristol Myers Squibb: Research Funding; GlaxoSmithKline: Consultancy; Adicet Bio: Consultancy; EUSA Bio: Consultancy.

*signifies non-member of ASH