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 - Funding Information:
PRECISIONS is primarily funded by the National Lung Heart and Blood Institute (grant number UH3HL145266 and U24HL145265), National Institutes of Health. Additional funding sources include the Three Lakes Foundation, which is a philanthropic organization with the mission of advancing care for IPF patients by supporting efforts to improve time to diagnosis and accelerate new treatments ( https://threelakesfoundation.org/ ). The Pulmonary Fibrosis Foundation is an integral collaborator for this clinical trial as PRECISIONS has the potential to demonstrate the utility of partnering with prospective cohorts to ensure clinical trial enrichment ( https://pulmonaryfibrosis.org/ ).
Funding Information:
We acknowledge Dr. Matthew Craig, Dr. Neil Aggarwal, and Dr. Barry Schmetter from the NHLBI for their support during the design and conduct of this trial. The following collaborators on the PRECISIONS study team contributed to study conception and data acquisition: Elizabeth Freiheit, Adam Martin-Schwarze, Ashley Szparza, Tanvi Naik, Rex Edwards, Gordon Bernard, Deborah Barnbaum, Joao de Andrade, Daren Knoell, Peter Lindenauer, Andre Rogatko, Marinella Temprosa, Shwu-Fan Ma, Emma Strickland, Jamie Sheth, Joyce Lee, Cheryl Nickerson-Nutter, David Lebo, Elizabeth Belloli, Candace Flaherty, Timothy Whelan, Max Lento, Amy Case, Ugonna Nwosu, Matthew Kottmann, Gerard Criner, Julie Juhas, Joshua Mooney, Jeanette Smith, Andrew Limper, Shannon Daley, Tessy Paul, Yousef Althulth, Chad Newton, Rhoda Annoh Gordon, Mary Strek, Spring Maleckar, Hyun Kim, Mandi DeGrote, Reba Blissell, Robert Kaner, Elizabeth Peters, Alicia Morris, Mark Hamblin, Carime Ward, Ryan Boente, Meghan Willig, Nitin Bhatt, Benjamin Hood, Cathleen Wilson, Sachin Chaudhary, Heidi Erickson, Haylie Lengel, Daniel Dilling, Sydney Montesi, Caroline Fromson, Toby Maher, Anoop Nambiar, Hilda Pomroy, Mary Beth Scholand, Chloe Kirkpatrick, Lisa Lancaster, Jim Del Greco, Stephen Sam Weigt, Eileen Callahan All authors reviewed the manuscript and are responsible for the conduct of the study. Data Coordinating Center (University of Michigan) – Cathie Spino, Kevin Flaherty, Susan Murray, Elizabeth Freiheit, Adam Martin-Schwarze, Ashley Szparza, Tanvi Naik, Rex Edwards. Data and Safety Monitoring Board – Gordon Bernard, Deborah Barnbaum, Joao de Andrade, Daren Knoell, Peter Lindenauer, Andre Rogatko, Marinella Temprosa. Biobank Core (University of Virginia) – Imre Noth, Shwu-Fan Ma, Emma Strickland. Clinical Events Committee – Jamie Sheth. Pulmonary Fibrosis Foundation – Joyce Lee. Three Lakes Foundation – Cheryl Nickerson-Nutter. Temple University Current Good Manufacturing Practices Services – David Lebo. University of Michigan – Elizabeth Belloli, Candace Flaherty. Medical University of South Carolina – Timothy Whelan, Max Lento. Piedmont Healthcare – Amy Case, Ugonna Nwosu. University of Rochester Medical Center – Matthew Kottmann. Temple University – Gerard Criner, Julie Juhas. Stanford University – Joshua Mooney, Jeanette Smith. Mayo Clinic – Andrew Limper, Shannon Daley. University of Virginia – Tessy Paul, Yousef Althulth. University of Texas Southwestern – Chad Newton, Rhoda Annoh Gordon. University of Chicago – Mary Strek, Spring Maleckar. University of Minnesota – Hyun Kim, Mandi DeGrote. University of Washington – Ganesh Raghu, Reba Blissell. Weill Cornell Medicine – Anna Podolanczuk, Robert Kaner, Elizabeth Peters, Alicia Morris. University of Kansas Medical Center – Mark Hamblin, Carime Ward. Indiana University – Ryan Boente, Meghan Willig. Ohio State University – Nitin Bhatt, Benjamin Hood. University of Arizona – Cathleen Wilson, Sachin Chaudhary, Heidi Erickson. University of Colorado – Joyce Lee, Haylie Lengel. Loyola University – Daniel Dilling. Massachusetts General Hospital – Sydney Montesi, Caroline Fromson. University of Southern California – Toby Maher. University of Texas San Antonio – Anoop Nambiar, Hilda Pomroy. University of Utath – Mary Beth Scholand, Chloe Kirkpatrick. Vanderbilt University – Lisa Lancaster, Jim Del Greco. University of California Los Angeles – Stephen Sam Weigt, Eileen Callahan.
Funding Information:
This work was supported by grants UH3HL145266 and U24HL145265 from the National Heart, Lung, and Blood Institute (NHLBI), Three Lakes Foundation, and Pulmonary Fibrosis Foundation. The study protocol has undergone full external peer review by the funding bodies as part of the peer review process. The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
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 -