TY - JOUR
T1 - Advancing precision medicine for acute respiratory distress syndrome
AU - Beitler, Jeremy R.
AU - Thompson, B. Taylor
AU - Baron, Rebecca M.
AU - Bastarache, Julie A.
AU - Denlinger, Loren C.
AU - Esserman, Laura
AU - Gong, Michelle N.
AU - LaVange, Lisa M.
AU - Lewis, Roger J.
AU - Marshall, John C.
AU - Martin, Thomas R.
AU - McAuley, Daniel F.
AU - Meyer, Nuala J.
AU - Moss, Marc
AU - Reineck, Lora A.
AU - Rubin, Eileen
AU - Schmidt, Eric P.
AU - Standiford, Theodore J.
AU - Ware, Lorraine B.
AU - Wong, Hector R.
AU - Aggarwal, Neil R.
AU - Calfee, Carolyn S.
N1 - Funding Information:
The workshop upon which this report is based was funded by the US National Heart, Lung, and Blood Institute (NHLBI). The NHLBI approved the workshop concept and provided administrative support for the workshop. All authors received reimbursement from the US National Institutes of Health for travel and accommodation to attend the workshop. RMB is funded by the US Department of Defense. JAB is funded by the US Department of Defense and the US Veterans Administration. DFM's institution has received funds for grants from the UK National Institute for Health Research, the Wellcome Trust, and Innovate UK. NJM has received funding from the Marcus Foundation. We would like to acknowledge the following additional contributors to the workshop from the NHLBI: Jim Kiley (attended the workshop and gave introductory remarks); Guofei Zhou, Aruna Natarajan, and Patricia Noel (provided suggestions for participants and speakers and attended the workshop); and Karen Bienstock and Rhonise Simpson (assisted with workshop planning and logistics and attended the workshop). We would also like to acknowledge the contribution of Christopher Leptak of the Food and Drug Administration, who attended the workshop and gave a talk on biomarker and drug development regulatory approval processes. The content of this manuscript is the responsibility of the authors alone and does not necessarily reflect the views or policies of the US Department of Veterans Affairs, the US Department of Health and Human Services, or the US Government.
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/1
Y1 - 2022/1
N2 - Acute respiratory distress syndrome (ARDS) is a heterogeneous clinical syndrome. Understanding of the complex pathways involved in lung injury pathogenesis, resolution, and repair has grown considerably in recent decades. Nevertheless, to date, only therapies targeting ventilation-induced lung injury have consistently proven beneficial, and despite these gains, ARDS morbidity and mortality remain high. Many candidate therapies with promise in preclinical studies have been ineffective in human trials, probably at least in part due to clinical and biological heterogeneity that modifies treatment responsiveness in human ARDS. A precision medicine approach to ARDS seeks to better account for this heterogeneity by matching therapies to subgroups of patients that are anticipated to be most likely to benefit, which initially might be identified in part by assessing for heterogeneity of treatment effect in clinical trials. In October 2019, the US National Heart, Lung, and Blood Institute convened a workshop of multidisciplinary experts to explore research opportunities and challenges for accelerating precision medicine in ARDS. Topics of discussion included the rationale and challenges for a precision medicine approach in ARDS, the roles of preclinical ARDS models in precision medicine, essential features of cohort studies to advance precision medicine, and novel approaches to clinical trials to support development and validation of a precision medicine strategy. In this Position Paper, we summarise workshop discussions, recommendations, and unresolved questions for advancing precision medicine in ARDS. Although the workshop took place before the COVID-19 pandemic began, the pandemic has highlighted the urgent need for precision therapies for ARDS as the global scientific community grapples with many of the key concepts, innovations, and challenges discussed at this workshop.
AB - Acute respiratory distress syndrome (ARDS) is a heterogeneous clinical syndrome. Understanding of the complex pathways involved in lung injury pathogenesis, resolution, and repair has grown considerably in recent decades. Nevertheless, to date, only therapies targeting ventilation-induced lung injury have consistently proven beneficial, and despite these gains, ARDS morbidity and mortality remain high. Many candidate therapies with promise in preclinical studies have been ineffective in human trials, probably at least in part due to clinical and biological heterogeneity that modifies treatment responsiveness in human ARDS. A precision medicine approach to ARDS seeks to better account for this heterogeneity by matching therapies to subgroups of patients that are anticipated to be most likely to benefit, which initially might be identified in part by assessing for heterogeneity of treatment effect in clinical trials. In October 2019, the US National Heart, Lung, and Blood Institute convened a workshop of multidisciplinary experts to explore research opportunities and challenges for accelerating precision medicine in ARDS. Topics of discussion included the rationale and challenges for a precision medicine approach in ARDS, the roles of preclinical ARDS models in precision medicine, essential features of cohort studies to advance precision medicine, and novel approaches to clinical trials to support development and validation of a precision medicine strategy. In this Position Paper, we summarise workshop discussions, recommendations, and unresolved questions for advancing precision medicine in ARDS. Although the workshop took place before the COVID-19 pandemic began, the pandemic has highlighted the urgent need for precision therapies for ARDS as the global scientific community grapples with many of the key concepts, innovations, and challenges discussed at this workshop.
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U2 - 10.1016/S2213-2600(21)00157-0
DO - 10.1016/S2213-2600(21)00157-0
M3 - Review article
C2 - 34310901
AN - SCOPUS:85121915287
SN - 2213-2600
VL - 10
SP - 107
EP - 120
JO - The Lancet Respiratory Medicine
JF - The Lancet Respiratory Medicine
IS - 1
ER -