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 - Funding Information:
Author contributions: T. J. K. S. L. T. F. Y. I. and H. H. are guarantors of integrity of the entire study; T. J. K. S. L. M. N. J. H. R. H. Y. L. T. F. K. K. B. J. M. G. H.-U. K. L. R. C. M. S.-P. C. P. and H. H. participated in the literature search; T. J. K. S. L. M. N. J. H. R. H. Y. L. J. V. Y. I. and H. H. contributed clinical studies; and T. J. K. S. L. M. N. W. D. T. J. H. R. H. Y. L. C. J. R. A. A. B. K. K. B. J. M. G. H.-U. K. D. A. L. A. G. N. L. R. C. M. S.-P. J. V. S. R. G. D. R. C. P. Y. I. and H. H. contributed to manuscript editing. All authors contributed to study concepts/study design or data acquisition or data analysis/interpretation, as well as manuscript drafting or manuscript revision for important intellectual content. All authors approved of the final version of the submitted manuscript, and all authors agree to ensure any questions related to the work are appropriately resolved. Financial/nonfinancial disclosures: The authors have reported to CHEST the following: K. S. L. receives royalties from Elsevier, Lippincott, and Springer. M. N. is a consultant for Daiichi Sankyo and AstraZeneca; has grants/grants pending with Merck, Canon Medical Systems, Daiichi Sankyo, and AstraZeneca; and received payment for lectures, including service on speaker bureaus from Roche. A. A. B. is a consultant for Daiichi Pharmaceutical and Olympus Medical; received payment for lectures, including service on speaker bureaus from Olympus Medical; and receives royalties from Elsevier. K. K. B. is DMC chair of Bioge and Humanetics; is a member of the scientific advisory board for Galecto, Third Pole, Galapagos, Boehringer Ingelheim, Theravance, Lifemax, Pliant, Blade Therapeutics, Open Source Imaging Consortium, Huitai Biomedicine, Lilly, Dispersol, and DevPro Biopharma; and has grants/grants pending with the National Heart, Lung, and Blood Institute. J. M. G. has grants/grants pending with Infinitt Healthcare and Dongkook Lifescience. H.-U. K. has grants/grants pending with Siemens, Philips, and Bayer; received payment for lectures, including service on speaker bureaus from Philips, AstraZeneca, Boehringer Ingelheim, and Merck, Sharp & Dohme. D. A. L. is a consultant for AstraZeneca, Boehringer Ingelheim, Daiichi Sankyo, and Parexel. A. G. N. is a consultant for Boehringer Ingelheim, Medical Quantitative Image Analysis, and Galapagos; received payment for lectures, including service on speaker bureaus from Boehringer Ingelheim; and received payment for development of educational presentations from UpToDate. L. R. is a consultant for Boehringer Ingelheim, Roche, Fibrogen, Promedior, Zambon, Veracyte, Respivant, MitoImmune, Pliant Therapeutics, Daewoo Pharmaceuticals, and DevPro Biopharma; has grants/grants pending with Boehringer Ingelheim; and received payment for lectures, including service on speaker bureaus from Boehringer Ingelheim, Cipla, and Roche. J. V. received payment for lectures, including service on speaker bureaus from Boehringer Ingelheim and Roche. S. R. is an employee of Lenox Hill Hospital; and receives royalties and payment for development of educational presentations from the American College of Chest Physicians. C. P. is a consultant for Daiichi Sankyo, AstraZeneca, and Siemens. H. H. is a consultant for Mitsubishi Chemical and Canon Medical Systems; and has grants/grants pending with Konica-Minolta and Canon Medical Systems. None declared: (T. J. W. D. T. J. H. R. H. Y. L. C. J. R. T. F. C.M.S.-P., G. D. R. Y. I.). Other contributions: The authors are grateful for the librarians Myung-Ah Shim and Jaero Park for their dedicated support of manuscript formatting. Both librarians are working at the Samsung Medical Information & Media Services of Samsung Medical Center located in Seoul, South Korea. Additional information: The e-Appendixes and e-Figures can be found in the Supplemental Materials section of the online article.
Publisher Copyright:
© 2021 The Authors
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 - 10.1016/j.chest.2020.11.027
DO - 10.1016/j.chest.2020.11.027
M3 - Article
C2 - 33434111
AN - SCOPUS:85101197264
SN - 0012-3692
VL - 159
SP - 1107
EP - 1125
JO - CHEST
JF - CHEST
IS - 3
ER -