Data from the MAGNITUDE trial support the positive benefit/risk profile of niraparib plus abiraterone acetate and prednisone as a treatment for those with BRCA-mutated metastatic castration-resistant prostate cancer.
Abiraterone acetate (Zytiga) plus prednisone (AAP) and niraparib improved overall survival (OS) compared with placebo plus AAP in those with metastatic castration resistant prostate cancer (mCRPC) harboring BRCA1/2 mutations, according to final analysis findings from the phase 3 MAGNITUDE trial (NCT03748641) presented at the 2023 European Society for Medical Oncology Congress (ESMO).1,2
The OS analysis occurred at a median follow-up of 35.9 months (19.2 additional months from the primary analysis). The analysis focused on patients with BRCA+ status, which included 113 patients who received niraparib plus AAP and 112 patients who received placebo plus AAP.
Data showed a median OS of 30.4 months among patients who received niraparib plus AAP, compared with 28.6 months among those who received placebo plus AAP (HR, 0.788; 95% CI, 0.554-1.120; nominal P = .1828). A pre-planned multivariate analysis of pre-specified prognostic factors, including those numerically off-balance at baseline, corroborated the OS benefit in the experimental arm (HR, 0.663; 95% CI, 0.464-0.947; nominal P = .0237).
Beyond OS, other secondary end points assessed in this final analysis included time to symptomatic progression (TSP), time to cytotoxic chemotherapy (TCC), and safety.3
Treatment with niraparib plus AAP was associated with benefits in both TSP (HR, 0.562; 95% CI, 0.371-0.849; nominal P = .0056) and TCC (HR, 0.598; 95% CI, 0.387-0.924; nominal P = .0192).
The median treatment duration was 20.5 months for those in the experimental arm and 14.4 months for those who received placebo plus AAP. Overall, 53.1% (60/113) of patients in the niraparib plus AAP arm discontinued treatment due to disease progression, compared with 76.8% (86/112) of patients in the placebo plus AAP arm.
There were no new safety signals that emerged from the longer follow-up. Adverse events were manageable in both arms, with differences driven by known hematologic toxicities associated with niraparib.
Previous findings from the primary analysis of the MAGNITUDE study showed an improvement in radiographic progression-free survival, the primary end point, with the combination of niraparib plus AAP compared with placebo/AAP in patients with BRCA+ mCRPC (HR, 0.53; 95% CI, 0.36-0.79; P = .001).4 These data led to the FDA-approval of the regimen in this setting.
“The final analysis of MAGNITUDE supports the positive benefit-risk profile of first-line niraparib with abiraterone acetate plus prednisone, establishing niraparib with abiraterone acetate plus prednisone as a new standard of care for patients with BRCA+ mCRPC,” said presenting author Kim Nguyen N. Chi, MD, FRCPC, a professor in the department of medicine at the University of British Columbia in Vancouver, Canada.