Nirogacestat, a γ-secretase inhibitor for desmoid tumors Journal Article


Authors: Gounder, M.; Ratan, R.; Alcindor, T.; Schöffski, P.; van der Graaf, W. T.; Wilky, B. A.; Riedel, R. F.; Lim, A.; Smith, L. M.; Moody, S.; Attia, S.; Chawla, S.; D'Amato, G.; Federman, N.; Merriam, P.; Van Tine, B. A.; Vincenzi, B.; Benson, C.; Bui, N. Q.; Chugh, R.; Tinoco, G.; Charlson, J.; Dileo, P.; Hartner, L.; Lapeire, L.; Mazzeo, F.; Palmerini, E.; Reichardt, P.; Stacchiotti, S.; Bailey, H. H.; Burgess, M. A.; Cote, G. M.; Davis, L. E.; Deshpande, H.; Gelderblom, H.; Grignani, G.; Loggers, E.; Philip, T.; Pressey, J. G.; Kummar, S.; Kasper, B.
Article Title: Nirogacestat, a γ-secretase inhibitor for desmoid tumors
Abstract: 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.) © 2023 Massachusetts Medical Society.
Keywords: genetics; hematology/oncology; treatments in oncology; genetics general; hematology/oncology general
Journal Title: New England Journal of Medicine
Volume: 388
Issue: 10
ISSN: 0028-4793
Publisher: Massachusetts Medical Society  
Date Published: 2023-03-09
Start Page: 898
End Page: 912
Language: English
DOI: 10.1056/NEJMoa2210140
PROVIDER: scopus
PUBMED: 36884323
PMCID: PMC11225596
DOI/URL:
Notes: Article -- MSK corresponding author is Mrinal Gounder --Source: Scopus
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  1. Mrinal M Gounder
    228 Gounder