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Nirogacestat, a γ-Secretase Inhibitor for Desmoid Tumors
- Gounder, Mrinal;
- Ratan, Ravin;
- Alcindor, Thierry;
- Schöffski, Patrick;
- van der Graaf, Winette T;
- Wilky, Breelyn A;
- Riedel, Richard F;
- Lim, Allison;
- Smith, L Mary;
- Moody, Stephanie;
- Attia, Steven;
- Chawla, Sant;
- D’Amato, Gina;
- Federman, Noah;
- Merriam, Priscilla;
- Van Tine, Brian A;
- Vincenzi, Bruno;
- Benson, Charlotte;
- Bui, Nam Quoc;
- Chugh, Rashmi;
- Tinoco, Gabriel;
- Charlson, John;
- Dileo, Palma;
- Hartner, Lee;
- Lapeire, Lore;
- Mazzeo, Filomena;
- Palmerini, Emanuela;
- Reichardt, Peter;
- Stacchiotti, Silvia;
- Bailey, Howard H;
- Burgess, Melissa A;
- Cote, Gregory M;
- Davis, Lara E;
- Deshpande, Hari;
- Gelderblom, Hans;
- Grignani, Giovanni;
- Loggers, Elizabeth;
- Philip, Tony;
- Pressey, Joseph G;
- Kummar, Shivaani;
- Kasper, Bernd
- et al.
Published Web Location
https://doi.org/10.1056/nejmoa2210140Abstract
Background
Desmoid tumors are rare, locally aggressive, highly recurrent soft-tissue tumors without approved treatments.Methods
We conducted a phase 3, international, double-blind, randomized, placebo-controlled trial of nirogacestat in adults with progressing desmoid tumors according to the Response Evaluation Criteria in Solid Tumors, version 1.1. Patients were assigned in a 1:1 ratio to receive the oral γ-secretase inhibitor nirogacestat (150 mg) or placebo twice daily. The primary end point was progression-free survival.Results
From May 2019 through August 2020, a total of 70 patients were assigned to receive nirogacestat and 72 to receive placebo. Nirogacestat had a significant progression-free survival benefit over placebo (hazard ratio for disease progression or death, 0.29; 95% confidence interval, 0.15 to 0.55; P<0.001); the likelihood of being event-free at 2 years was 76% with nirogacestat and 44% with placebo. Between-group differences in progression-free survival were consistent across prespecified subgroups. The percentage of patients who had an objective response was significantly higher with nirogacestat than with placebo (41% vs. 8%; P<0.001), with a median time to response of 5.6 months and 11.1 months, respectively; the percentage of patients with a complete response was 7% and 0%, respectively. Significant between-group differences in secondary patient-reported outcomes, including pain, symptom burden, physical or role functioning, and health-related quality of life, were observed (P≤0.01). Frequent adverse events with nirogacestat included diarrhea (in 84% of the patients), nausea (in 54%), fatigue (in 51%), hypophosphatemia (in 42%), and maculopapular rash (in 32%); 95% of adverse events were of grade 1 or 2. Among women of childbearing potential receiving nirogacestat, 27 of 36 (75%) had adverse events consistent with ovarian dysfunction, which resolved in 20 women (74%).Conclusions
Nirogacestat was associated with significant benefits with respect to progression-free survival, objective response, pain, symptom burden, physical functioning, role functioning, and health-related quality of life in adults with progressing desmoid tumors. Adverse events with nirogacestat were frequent but mostly low grade. (Funded by SpringWorks Therapeutics; DeFi ClinicalTrials.gov number, NCT03785964.).Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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