TY - JOUR
T1 - Design and rationale for the prospective treatment efficacy in IPF using genotype for NAC selection (PRECISIONS) clinical trial
AU - for the PRECISIONS Study Team
AU - Podolanczuk, Anna J.
AU - Kim, John S.
AU - Cooper, Christopher B.
AU - Lasky, Joseph A.
AU - Murray, Susan
AU - Oldham, Justin M.
AU - Raghu, Ganesh
AU - Flaherty, Kevin R.
AU - Spino, Cathie
AU - Noth, Imre
AU - Martinez, Fernando J.
AU - Freiheit, Elizabeth
AU - Martin-Schwarze, Adam
AU - Szparza, Ashley
AU - Naik, Tanvi
AU - Edwards, Rex
AU - Bernard, Gordon
AU - Barnbaum, Deborah
AU - de Andrade, Joao
AU - Knoell, Daren
AU - Lindenauer, Peter
AU - Rogatko, Andre
AU - Temprosa, Marinella
AU - Ma, Shwu Fan
AU - Strickland, Emma
AU - Sheth, Jamie
AU - Lee, Joyce
AU - Nickerson-Nutter, Cheryl
AU - Lebo, David
AU - Belloli, Elizabeth
AU - Flaherty, Candace
AU - Whelan, Timothy
AU - Lento, Max
AU - Case, Amy
AU - Nwosu, Ugonna
AU - Kottmann, Matthew
AU - Criner, Gerard
AU - Juhas, Julie
AU - Mooney, Joshua
AU - Smith, Jeanette
AU - Limper, Andrew
AU - Daley, Shannon
AU - Paul, Tessy
AU - Althulth, Yousef
AU - Newton, Chad
AU - Gordon, Rhoda Annoh
AU - Strek, Mary
AU - Maleckar, Spring
AU - Kim, Hyun
AU - DeGrote, Mandi
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease with few treatment options. N-acetylcysteine (NAC) is a well-tolerated, inexpensive treatment with antioxidant and anti-fibrotic properties. The National Heart, Lung, and Blood Institute (NHLBI)-sponsored PANTHER (Prednisone Azathioprine and NAC therapy in IPF) trial confirmed the harmful effects of immunosuppression in IPF, and did not show a benefit to treatment with NAC. However, a post hoc analysis revealed a potential beneficial effect of NAC in a subgroup of individuals carrying a specific genetic variant, TOLLIP rs3750920 TT genotype, present in about 25% of patients with IPF. Here, we present the design and rationale for the Phase III, multi-center, randomized, double-blind, placebo-controlled Prospective Treatment Efficacy in IPF Using Genotype for NAC Selection (PRECISIONS) clinical trial. Methods: The PRECISIONS trial will randomize 200 patients with IPF and the TOLLIP rs3750920 TT genotype 1:1 to oral N-acetylcysteine (600 mg tablets taken three times a day) or placebo for a 24-month duration. The primary endpoint is the composite of time to 10% relative decline in forced vital capacity (FVC), first respiratory hospitalization, lung transplantation, or death from any cause. Secondary endpoints include change in patient-reported outcome scores and proportion of participants with treatment-emergent adverse events. Biospecimens, including blood, buccal, and fecal will be collected longitudinally for future research purposes. Study participants will be offered enrollment in a home spirometry substudy, which explores time to 10% relative FVC decline measured at home, and its comparison with study visit FVC. Discussion: The sentinel observation of a potential pharmacogenetic interaction between NAC and TOLLIP polymorphism highlights the urgent, unmet need for better, molecularly focused, and precise therapeutic strategies in IPF. The PRECISIONS clinical trial is the first study to use molecularly-focused techniques to identify patients with IPF most likely to benefit from treatment. PRECISIONS has the potential to shift the paradigm in how trials in this condition are designed and executed, and is the first step toward personalized medicine for patients with IPF. Trial Registration ClinicalTrials.gov identifier: NCT04300920. Registered March 9, 2020. https://clinicaltrials.gov/ct2/show/NCT04300920
AB - Background: Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease with few treatment options. N-acetylcysteine (NAC) is a well-tolerated, inexpensive treatment with antioxidant and anti-fibrotic properties. The National Heart, Lung, and Blood Institute (NHLBI)-sponsored PANTHER (Prednisone Azathioprine and NAC therapy in IPF) trial confirmed the harmful effects of immunosuppression in IPF, and did not show a benefit to treatment with NAC. However, a post hoc analysis revealed a potential beneficial effect of NAC in a subgroup of individuals carrying a specific genetic variant, TOLLIP rs3750920 TT genotype, present in about 25% of patients with IPF. Here, we present the design and rationale for the Phase III, multi-center, randomized, double-blind, placebo-controlled Prospective Treatment Efficacy in IPF Using Genotype for NAC Selection (PRECISIONS) clinical trial. Methods: The PRECISIONS trial will randomize 200 patients with IPF and the TOLLIP rs3750920 TT genotype 1:1 to oral N-acetylcysteine (600 mg tablets taken three times a day) or placebo for a 24-month duration. The primary endpoint is the composite of time to 10% relative decline in forced vital capacity (FVC), first respiratory hospitalization, lung transplantation, or death from any cause. Secondary endpoints include change in patient-reported outcome scores and proportion of participants with treatment-emergent adverse events. Biospecimens, including blood, buccal, and fecal will be collected longitudinally for future research purposes. Study participants will be offered enrollment in a home spirometry substudy, which explores time to 10% relative FVC decline measured at home, and its comparison with study visit FVC. Discussion: The sentinel observation of a potential pharmacogenetic interaction between NAC and TOLLIP polymorphism highlights the urgent, unmet need for better, molecularly focused, and precise therapeutic strategies in IPF. The PRECISIONS clinical trial is the first study to use molecularly-focused techniques to identify patients with IPF most likely to benefit from treatment. PRECISIONS has the potential to shift the paradigm in how trials in this condition are designed and executed, and is the first step toward personalized medicine for patients with IPF. Trial Registration ClinicalTrials.gov identifier: NCT04300920. Registered March 9, 2020. https://clinicaltrials.gov/ct2/show/NCT04300920
KW - Clinical trial
KW - IPF
KW - N-acetylcysteine
KW - Protocol
UR - http://www.scopus.com/inward/record.url?scp=85143889426&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85143889426&partnerID=8YFLogxK
U2 - 10.1186/s12890-022-02281-8
DO - 10.1186/s12890-022-02281-8
M3 - Article
C2 - 36514019
AN - SCOPUS:85143889426
SN - 1471-2466
VL - 22
JO - BMC Pulmonary Medicine
JF - BMC Pulmonary Medicine
IS - 1
M1 - 475
ER -