TY - JOUR
T1 - Chest CT diagnosis and clinical management of drug-related pneumonitis in patients receiving molecular targeting agents and immune checkpoint inhibitors
T2 - A position paper from the fleischner society
AU - Johkoh, Takeshi
AU - Lee, Kyung Soo
AU - Nishino, Mizuki
AU - Travis, William D.
AU - Ryu, Jay H.
AU - Lee, Ho Yun
AU - Ryerson, Christopher J.
AU - Franquet, Tomás
AU - Bankier, Alexander A.
AU - Brown, Kevin K.
AU - Goo, Jin Mo
AU - Kauczor, Hans Ulrich
AU - Lynch, David A.
AU - Nicholson, Andrew G.
AU - Richeldi, Luca
AU - Schaefer-Prokop, Cornelia M.
AU - Verschakelen, Johny
AU - Raoof, Suhail
AU - Rubin, Geoffrey D.
AU - Powell, Charles
AU - Inoue, Yoshikazu
AU - Hatabu, Hiroto
N1 - Publisher Copyright:
© 2021 Radiological Society of North America Inc.. All rights reserved.
PY - 2021/3
Y1 - 2021/3
N2 - Use of molecular targeting agents and immune checkpoint inhibitors (ICIs) has increased the frequency and broadened the spectrum of lung toxicity, particularly in patients with cancer. The diagnosis of drug-related pneumonitis (DRP) is usually achieved by excluding other potential known causes. Awareness of the incidence and risk factors for DRP is becoming increasingly important. The severity of symptoms associated with DRP may range from mild or none to life-threatening with rapid progression to death. Imaging features of DRP should be assessed in consideration of the distribution of lung parenchymal abnormalities (radiologic pattern approach). The CT patterns reflect acute (diffuse alveolar damage) interstitial pneumonia and transient (simple pulmonary eosinophilia) lung abnormality, subacute interstitial disease (organizing pneumonia and hypersensitivity pneumonitis), and chronic interstitial disease (nonspecific interstitial pneumonia). A single drug can be associated with multiple radiologic patterns. Treatment of a patient suspected of having DRP generally consists of drug discontinuation, immunosuppressive therapy, or both, along with supportive measures eventually including supplemental oxygen and intensive care. In this position paper, the authors provide diagnostic criteria and management recommendations for DRP that should be of interest to radiologists, clinicians, clinical trialists, and trial sponsors, among others.
AB - Use of molecular targeting agents and immune checkpoint inhibitors (ICIs) has increased the frequency and broadened the spectrum of lung toxicity, particularly in patients with cancer. The diagnosis of drug-related pneumonitis (DRP) is usually achieved by excluding other potential known causes. Awareness of the incidence and risk factors for DRP is becoming increasingly important. The severity of symptoms associated with DRP may range from mild or none to life-threatening with rapid progression to death. Imaging features of DRP should be assessed in consideration of the distribution of lung parenchymal abnormalities (radiologic pattern approach). The CT patterns reflect acute (diffuse alveolar damage) interstitial pneumonia and transient (simple pulmonary eosinophilia) lung abnormality, subacute interstitial disease (organizing pneumonia and hypersensitivity pneumonitis), and chronic interstitial disease (nonspecific interstitial pneumonia). A single drug can be associated with multiple radiologic patterns. Treatment of a patient suspected of having DRP generally consists of drug discontinuation, immunosuppressive therapy, or both, along with supportive measures eventually including supplemental oxygen and intensive care. In this position paper, the authors provide diagnostic criteria and management recommendations for DRP that should be of interest to radiologists, clinicians, clinical trialists, and trial sponsors, among others.
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U2 - 10.1148/radiol.2021203427
DO - 10.1148/radiol.2021203427
M3 - Review article
C2 - 33434111
AN - SCOPUS:85101915901
SN - 0033-8419
VL - 298
SP - 550
EP - 566
JO - Radiology
JF - Radiology
IS - 3
ER -