Background:

In CARTITUDE-4, a phase 3 open-label randomized controlled trial, CARVYKTI (ciltacabtagene autoleucel; cilta-cel), demonstrated superior progression-free survival (PFS) and response rates over physician's choice of daratumumab, pomalidomide and dexamethasone [DPd], or pomalidomide, bortezomib and dexamethasone [PVd].Recently an updated prespecified analysis of CARTITUDE-4 with median follow-up of 34 months demonstrated significant overall survival (OS) benefit of cilta-cel vs physician's choice in patients with relapsed and refractory multiple myeloma (RRMM) who are refractory to lenalidomide and have received 1-3 prior line(s) of therapy (LOTs) including an immunomodulatory agent (IMiD) and a proteasome inhibitor (PI). The objective of this abstract is to evaluate the comparative efficacy of cilta-cel vs. a combined group of alternative treatments pooled from daratumumab clinical trials in this target population.

Methods:

Patient-level data were available for patients from CARTITUDE-4 who received cilta-cel, and from nine daratumumab trials (CASTOR, CANDOR, APOLLO, ALCYONE, MAIA, GRIFFIN, CASSIOPEIA, POLLUX and EQUULEUS) who received active or subsequent treatments with or without daratumumab. Patients from the daratumumab clinical trials had either newly diagnosed MM (NDMM) or RRMM at study enrolment. Patients were included in the comparator cohort if they satisfied the key eligibility criteria of CARTITUDE-4 at enrollment or at a subsequent line of therapy. Inverse probability of treatment weighting was used to adjust for imbalances between cohorts on key patient characteristics. OS, PFS, real-world PFS (RW-PFS), time to next treatment (TTNT), overall response rate (ORR), very good partial response or better rate (≥VGPR), complete response or better rate (≥CR), were assessed. Sensitivity analyses were conducted using different analytical methods and additional patient characteristics.

Results:

The cilta-cel cohort consisted of 208 patients in the CARTITUDE-4 trial and the combined comparator cohort included 800 patients from the daratumumab trials (who fulfilled the key eligibility criteria for CARTITUDE-4). In this combined comparator cohort, the most frequent treatment regimens used were carfilzomib and dexamethasone [Kd], daratumumab with Kd [DKd], pomalidomide and dexamethasone [Pd], and DPd, among others. After adjustment, baseline covariates were similar across the cohorts. In this updated analysis, Cilta-cel demonstrated significant OS benefit, reducing the risk of death by 71% (OS hazard ratio [HR]: 0.29; 95% CI: 0.20-0.41) and showed significant PFS superiority, reducing the risk of disease progression or death by 67% (PFS HR: 0.33; 95% CI: 0.24-0.46) and by 74% (RW-PFS HR: 0.26; 95% CI: 0.19-0.35), whilst reducing the risk of progression, death or next treatment by 74% (TTNT HR: 0.26; 95% CI: 0.19-0.36). Cilta-cel demonstrated improved ORR (odds ratio [OR]: 3.60; 95% CI: 2.26-5.82), ≥VGPR (OR: 8.09; 95% CI: 5.16-12.89), and deep improvement of ≥CR (OR: 20.92; 95% CI: 12.57-36.02) vs. the comparator cohort. All results were statistically significant (p<0.0001) and consistent across sensitivity analyses.

Conclusion:

In this analysis cilta-cel confirmed the superior efficacy compared to alternative treatments from this pooled comparator cohort across all efficacy outcomes, particularly overall survival, highlighting the potential for cilta-cel to be considered a new standard of care option for lenalidomide-refractory RRMM patients, who have received 1-3 prior LOTs, including an IMiD and a PI.

Disclosures

Delforge:Amgen, BMS, GSJ, Janssen, Sanofi, Pfizer, Roche: Honoraria; Amgen, BMS, GSJ, Janssen, Sanofi, Pfizer, F. Hoffmann-La Roche Ltd: Consultancy; University Hospital Leuven: Consultancy, Honoraria; Janssen: Consultancy, Honoraria; BMS: Consultancy, Honoraria; GSK: Consultancy, Honoraria; Sanofi: Consultancy, Honoraria; Roche: Consultancy, Honoraria. Avivi Mazza:AbbVie: Consultancy, Honoraria; Novartis: Consultancy, Honoraria. Mateos:BMS/Celgene, Janssen-Cilag, Sanofi, Abbvie, Stemline, Oncopeptides, GSK: Honoraria, Membership on an entity's Board of Directors or advisory committees; Amgen, Takeda, Regeneron: Honoraria. Qi:J&J: Current Employment, Current equity holder in publicly-traded company. Mendes:Johnson & Johnson: Current Employment. Lee:Janssen: Current Employment, Current equity holder in publicly-traded company. Schecter:Johnson and Johnson Innovative Medicine: Current Employment, Current holder of stock options in a privately-held company. Deraedt:Janssen: Current Employment, Current equity holder in publicly-traded company. Lonardi:J&J Innovative Medicine: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Slaughter:Johnson & Johnson Innovative Medicine: Current Employment, Current equity holder in private company, Current holder of stock options in a privately-held company. Connors:J&J: Current Employment. Patel:Legend Biotech, GSK, Freeline, BMS (spouse), AbbVie (spouse): Current Employment, Current equity holder in publicly-traded company, Current holder of stock options in a privately-held company, Divested equity in a private or publicly-traded company in the past 24 months, Ended employment in the past 24 months. Florendo:Legend Biotech: Current Employment. Einsele:BMS: Honoraria; Amgen: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Celgene/Bristol-Meyers Squibb: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Sanofi: Honoraria; Novartis: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Takeda: Honoraria, Membership on an entity's Board of Directors or advisory committees. Dhakal:Bristol Myers Squibb: Honoraria, Research Funding; Medical College of Wisconsin: Current Employment; Janssen: Honoraria, Research Funding, Speakers Bureau; Acrellx: Research Funding; Pfizer: Consultancy, Honoraria, Speakers Bureau; Carsgen: Research Funding; Genentech: Consultancy, Honoraria; C4 therapeutics: Research Funding; Karyopharm: Honoraria, Speakers Bureau; Sanofi: Research Funding. Roeloffzen:Abbvie: Other: Travel expenses; BMS: Membership on an entity's Board of Directors or advisory committees; Amgen: Honoraria; Sanofi: Other: Travel expenses, Speakers Bureau; Janssen-Cilag: Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Travel expenses, Speakers Bureau.

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