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Nirogacestat, a γ-Secretase Inhibitor for Desmoid Tumors.

Authors :
Gounder M
Ratan R
Alcindor T
Schöffski P
van der Graaf WT
Wilky BA
Riedel RF
Lim A
Smith LM
Moody S
Attia S
Chawla S
D'Amato G
Federman N
Merriam P
Van Tine BA
Vincenzi B
Benson C
Bui NQ
Chugh R
Tinoco G
Charlson J
Dileo P
Hartner L
Lapeire L
Mazzeo F
Palmerini E
Reichardt P
Stacchiotti S
Bailey HH
Burgess MA
Cote GM
Davis LE
Deshpande H
Gelderblom H
Grignani G
Loggers E
Philip T
Pressey JG
Kummar S
Kasper B
Source :
The New England journal of medicine [N Engl J Med] 2023 Mar 09; Vol. 388 (10), pp. 898-912.
Publication Year :
2023

Abstract

Background: Desmoid tumors are rare, locally aggressive, highly recurrent soft-tissue tumors without approved treatments.<br />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.<br />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%).<br />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.).<br /> (Copyright © 2023 Massachusetts Medical Society.)

Details

Language :
English
ISSN :
1533-4406
Volume :
388
Issue :
10
Database :
MEDLINE
Journal :
The New England journal of medicine
Publication Type :
Academic Journal
Accession number :
36884323
Full Text :
https://doi.org/10.1056/NEJMoa2210140