TY - JOUR
T1 - Radiographic features and poor prognostic factors of interstitial lung disease with nivolumab for non–small cell lung cancer
AU - Saito, Yoshinobu
AU - Sasaki, Shinichi
AU - Oikado, Katsunori
AU - Tominaga, Junya
AU - Sata, Masafumi
AU - Sakai, Fumikazu
AU - Kato, Terufumi
AU - Iwasawa, Tae
AU - Kenmotsu, Hirotsugu
AU - Kusumoto, Masahiko
AU - Baba, Tomohisa
AU - Endo, Masahiro
AU - Fujiwara, Yutaka
AU - Sugiura, Hiroaki
AU - Yanagawa, Noriyo
AU - Ito, Yoshihiko
AU - Sakamoto, Takahiko
AU - Ohe, Yuichiro
AU - Kuwano, Kazuyoshi
N1 - Funding Information:
This work was supported by Ono Pharmaceutical Co., Ltd. and Bristol‐Myers Squibb K.K. Medical writing assistance was provided by Sandra Kurian, MPharm, and Tania Dickson, PhD, CMPP, of ProScribe – Envision Pharma Group and was funded by Ono Pharmaceutical Co., Ltd. and Bristol‐Myers Squibb K.K. ProScribe's services complied with international guidelines for Good Publication Practice (GPP3).
Funding Information:
Y. Saito reports personal fees from AstraZeneca, Boehringer Ingelheim, Chugai, Novartis, and Ono. S. Sasaki reports personal fees and/or grants from Boehringer Ingelheim, Chugai, Kyorin, MSD, Ono, Pfizer, Shionogi, Taiho, and Torii. K. Oikado, J. Tominaga, M. Sata, and M. Endo report personal fees from Ono. F. Sakai reports personal fees and/or grants and/or nonfinancial support from AstraZeneca, Bayer, BMS, Boehringer Ingelheim, Daiichi Sankyo, Eisai, Fuji, Japanese Ministry of Health, Labour and Welfare, Japanese Ministry of the Environment, Merck Serono, Ono, Shionogi, and Canon Medical Systems. T. Kato reports personal fees and/or grants from AbbVie, Astellas, AstraZeneca, BMS, Boehringer Ingelheim, Chugai, Eli Lilly, F. Hoffmann‐La Roche, Kyorin, Kyowa Kirin, MSD, Merck Serono, Nitto Denko, Novartis, Ono, Pfizer, Regeneron, Sumitomo Dainippon, Taiho, and Takeda. T. Iwasawa reports personal fees and/or grants from AstraZeneca, Bayer, Boehringer Ingelheim, Canon Medical Systems, FujiFilm Medical Systems, GE Healthcare, KAKENHI, Nihon Medi‐Physics, Ono, Shionogi, and Tsuchiya Foundation. H. Kenmotsu reports personal fees and/or grants from AstraZeneca, Boehringer Ingelheim, BMS, Chugai, Eli Lilly, Kyowa Hakko Kirin, MSD, Novartis, Ono, and Taiho. M. Kusumoto reports personal fees from AstraZeneca, Canon Medical Systems, MSD, and Ono. T. Baba reports personal fees and/or nonfinancial support from AMCO, Asahi Kasei, Astellas, AstraZeneca, BMS, Boehringer Ingelheim, Boston Scientific, Daiichi Sankyo, Kyorin, MSD, Ono, Shionogi, Taiho, and Toray Industries. Y. Fujiwara reports grants and/or personal fees from AbbVie, AstraZeneca, BMS, Chugai, Daiichi Sankyo, Eisai, Eli Lilly, Incyte, Merck Serono, MSD, Novartis, Ono, Sysmex, and Taiho. H. Sugiura reports personal fees from Ono and MSD. N. Yanagawa reports personal fees and/or grants and/or nonfinancial support from Ono. Y. Ito and T. Sakamoto are employed by Ono. Y. Ohe reports personal fees and/or grants from Amgen, AstraZeneca, Bayer, BMS, Boehringer Ingelheim, Celltrion, Chugai, Daiichi Sankyo, Dainippon‐Sumitomo, Eli Lilly, Ignyta, Janssen, Kissei, Kyorin, MSD, Novartis, Ono, Pfizer, Taiho, and Takeda. K. Kuwano reports personal fees and/or grants from Astellas, AstraZeneca, Boehringer Ingelheim, Chugai, Daiichi Sankyo, Eisai, GSK, Kyorin, MSD, Ono, Shionogi, Taiho, and Tsumura.
Publisher Copyright:
© 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2021/4
Y1 - 2021/4
N2 - Nivolumab can cause interstitial lung disease (ILD), which may be fatal; however, mortality risk factors have not been identified. This postmarketing study evaluated the poor prognostic factors of ILD in nivolumab-treated patients with non–small cell lung cancer (NSCLC) in Japan. Clinical and chest imaging findings for each ILD case were assessed by an expert central review committee, and prognosis was evaluated by radiographic findings, including the presence/absence of peritumoral ground-glass opacity (peritumoral-GGO). Poor prognostic factors were identified by univariate and multivariate Cox regression analysis. Of the 238 patients with nivolumab-induced ILD, 37 died. The main radiographic patterns of ILD were cryptogenic organizing pneumonia/chronic eosinophilic pneumonia–like (53.4%), faint infiltration pattern/acute hypersensitivity pneumonia–like (20.2%), diffuse alveolar damage (DAD)-like (10.9%), and nonspecific interstitial pneumonia–like (6.3%). The main poor prognostic factors identified were DAD-like pattern (highest hazard ratio: 10.72), ≤60 days from the start of nivolumab treatment to the onset of ILD, pleural effusion before treatment, lesion distribution contralateral or bilateral to the tumor, and abnormal change in C-reactive protein (CRP) levels. Of the 37 deaths due to ILD, 17 had DAD-like radiographic pattern, three had peritumoral-GGO, and five had a change in radiographic pattern from non-DAD at the onset to DAD-like. Patients with NSCLC who develop ILD during nivolumab treatment should be managed carefully if they have poor prognostic factors such as DAD-like radiographic pattern, onset of ILD ≤60 days from nivolumab initiation, pleural effusion before nivolumab treatment, lesion distribution contralateral or bilateral to the tumor, and abnormal changes in CRP levels.
AB - Nivolumab can cause interstitial lung disease (ILD), which may be fatal; however, mortality risk factors have not been identified. This postmarketing study evaluated the poor prognostic factors of ILD in nivolumab-treated patients with non–small cell lung cancer (NSCLC) in Japan. Clinical and chest imaging findings for each ILD case were assessed by an expert central review committee, and prognosis was evaluated by radiographic findings, including the presence/absence of peritumoral ground-glass opacity (peritumoral-GGO). Poor prognostic factors were identified by univariate and multivariate Cox regression analysis. Of the 238 patients with nivolumab-induced ILD, 37 died. The main radiographic patterns of ILD were cryptogenic organizing pneumonia/chronic eosinophilic pneumonia–like (53.4%), faint infiltration pattern/acute hypersensitivity pneumonia–like (20.2%), diffuse alveolar damage (DAD)-like (10.9%), and nonspecific interstitial pneumonia–like (6.3%). The main poor prognostic factors identified were DAD-like pattern (highest hazard ratio: 10.72), ≤60 days from the start of nivolumab treatment to the onset of ILD, pleural effusion before treatment, lesion distribution contralateral or bilateral to the tumor, and abnormal change in C-reactive protein (CRP) levels. Of the 37 deaths due to ILD, 17 had DAD-like radiographic pattern, three had peritumoral-GGO, and five had a change in radiographic pattern from non-DAD at the onset to DAD-like. Patients with NSCLC who develop ILD during nivolumab treatment should be managed carefully if they have poor prognostic factors such as DAD-like radiographic pattern, onset of ILD ≤60 days from nivolumab initiation, pleural effusion before nivolumab treatment, lesion distribution contralateral or bilateral to the tumor, and abnormal changes in CRP levels.
KW - computed X-ray tomography
KW - interstitial lung diseases
KW - nivolumab
KW - non-small-cell lung carcinoma
KW - prognostic factors
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U2 - 10.1111/cas.14710
DO - 10.1111/cas.14710
M3 - Article
C2 - 33098725
AN - SCOPUS:85101363503
SN - 1347-9032
VL - 112
SP - 1495
EP - 1505
JO - Cancer Science
JF - Cancer Science
IS - 4
ER -