Abstract 434P
Background
Although many reports classify drug-induced pneumonitis based on the tumour type or drug category, mortality of drug-induced pneumonitis across tumour types or drug categories at high-volume cancer centres are rarely reported.
Methods
From January 2014 to December 2018, we reviewed patients who experienced drug-induced pneumonitis requiring hospitalization. We collected the patient’s background, clinical and radiological features, and outcome of treatment for drug-induced pneumonitis. To evaluate the risk factors of death from drug-induced pneumonitis, we conducted a multivariate analysis of the history of interstitial lung disease, drug-induced pneumonitis, lung surgery, chest radiotherapy, performance status, oxygen supplementation, and traction bronchiectasis on computed tomography (CT) at diagnosis as explanatory variables.
Results
A total of 129 patients experienced drug-induced pneumonitis in the study period. The median age (range) was 72 years (25–86 years). There were 60 men (69.8%) and 39 women (30.2%). The number of patients with lung cancer, breast cancer, biliary tract and pancreatic cancer, upper gastrointestinal tract cancer, lower gastrointestinal tract cancer, melanoma, and other cancers were 70,11,11,10,9,8,10, respectively. According to the clinician, drug-induced pneumonitis was induced by immune-checkpoint inhibitors (ICI), molecular targeted agents (TKI), and cytotoxic agents (CTX) in 26, 22, 81 patients, respectively. Among patients with drug-induced pneumonitis requiring hospitalization, a total of 15 (11.6%) patients (ICIs: 2 [7.6%]; TKIs: 1 [4.5%]; CTX: 12 [14.8%]) died because of drug-induced pneumonitis. A logistic regression analysis revealed a history of chest radiotherapy and lung surgery, poor performance status, and traction bronchiectasis on CT at diagnosis as the independent risk factors for mortality in drug-induced pneumonitis requiring hospitalization.
Conclusions
The mortality rate of drug-induced pneumonitis requiring hospitalization was 11.6% and tended to vary with the antineoplastic agent. In patients hospitalized because of drug-induced pneumonitis, history of lung surgery and chest radiotherapy and traction bronchiectasis on CT indicated poor prognosis.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
H. Horinouchi: Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): BMS; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): MSD; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Chugai; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Taiho; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): AstraZeneca; Research grant / Funding (self), Research grant / Funding (institution): Astellas; Research grant / Funding (self), Research grant / Funding (institution): Merck Serono; Research grant / Funding (self), Research grant / Funding (institution): Genomic Health; Honoraria (self): Lilly. K. Tamura: Research grant / Funding (self), Research grant / Funding (institution): Pfizer; Research grant / Funding (self), Research grant / Funding (institution): Daiichi Sankyo; Research grant / Funding (self), Research grant / Funding (institution): MSD; Research grant / Funding (self), Research grant / Funding (institution): Eli Lilly; Research grant / Funding (self), Research grant / Funding (institution): Eisai; Research grant / Funding (self), Research grant / Funding (institution): Cyugai; Research grant / Funding (self), Research grant / Funding (institution): Ono. T. Okusaka: Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Novartis Pharma K.K.; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Ono Pharmaceutical Co., Ltd.; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Eisai Co., Ltd.; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Eli Lilly Japan K.K; Honoraria (self), Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): Taiho Pharmaceutical Co., Ltd.; Honoraria (self): Yakult Honsha Co., Ltd.; Honoraria (self): Teijin Pharma Ltd; Honoraria (self): Shire; Honoraria (self): AbbVie Inc; Honoraria (self), Advisory / Consultancy: Daiichi Sankyo Co., Ltd.; Honoraria (self): Takeda Pharmaceutical Co., Ltd.; Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): Dainippon Sumitomo Pharma Co., Ltd.; Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): Bristol-Myers Squibb. K.K.; Research grant / Funding (self), Research grant / Funding (institution): Pfizer Japan Inc.; Research grant / Funding (self), Research grant / Funding (institution): Kyowa Hakko Kirin Co., Ltd.; Research grant / Funding (self), Research grant / Funding (institution): AstraZeneca K.K.; Research grant / Funding (self), Research grant / Funding (institution): Chugai Pharmaceutical Co., Ltd.; Research grant / Funding (self), Research grant / Funding (institution): Nano Carrier Co., Ltd.; Research grant / Funding (self), Research grant / Funding (institution): Baxter. N. Boku: Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Taiho; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Ono; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Bristol Myers-Squibb; Honoraria (self): Chugai; Honoraria (self): Eli-Lilly. N. Yamazaki: Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): ONO Pharmaceuticals; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Bristol-Myers Squibb; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Novartis Pharma K.K.; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): MSD K.K.; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Merck Serono Co., Ltd.; Honoraria (self): Takeda Pharmaceutical Co., Ltd.; Honoraria (self): Chugai Pharmaceutical Co., Ltd.; Research grant / Funding (self), Research grant / Funding (institution): Takara-bio. Y. Ohe: Honoraria (self), Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): AstraZeneca; Honoraria (self), Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): Chugai; Honoraria (self), Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): ONO; Honoraria (self), Leadership role, Research grant / Funding (self), Research grant / Funding (institution): BMS; Advisory / Consultancy, Research grant / Funding (self), Research grant / Funding (institution): Kyorin; Advisory / Consultancy: Celltrion; Advisory / Consultancy: Amgen; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Lilly; Honoraria (self): Boehringer Ingelheim; Honoraria (self): Bayer; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Pfizer; Honoraria (self): MSD; Honoraria (self), Research grant / Funding (self), Research grant / Funding (institution): Taiho; Research grant / Funding (self), Research grant / Funding (institution): Dainippon- Sumitomo; Research grant / Funding (self), Research grant / Funding (institution): Novartis; Research grant / Funding (self), Research grant / Funding (institution): Kissei; Research grant / Funding (self), Research grant / Funding (institution): Ignyta; Research grant / Funding (self), Research grant / Funding (institution): Takeda; Research grant / Funding (self), Research grant / Funding (institution): Kissei; Research grant / Funding (self), Research grant / Funding (institution): Daiichi-Sankyo. M. Kusumoto: Honoraria (self): Ono pharmaceutical Co. Ltd.; Honoraria (self): AstraZeneca K.K; Honoraria (self): MSD K.K; Research grant / Funding (self), Research grant / Funding (institution): Canon medical systems corporation. All other authors have declared no conflicts of interest.
Resources from the same session
504P - A single center report for safety and efficacy of CT-707 in Chinese patients with advanced, anaplastic lymphoma kinase-rearranged non-small cell lung cancer or other tumours
Presenter: Peng Song
Session: Poster display session
Resources:
Abstract
519P - Initial results of lung cancer genomic screening project for individualized medicine in Asia: LC-SCRUM-Asia
Presenter: Chih-Hsi Kuo
Session: Poster display session
Resources:
Abstract
521P - A randomized, phase II study comparing irinotecan versus amrubicin as maintenance therapy after first-line induction therapy for extensive disease small cell lung cancer (HOT1401/NJLCG1401)
Presenter: Keisuke Baba
Session: Poster display session
Resources:
Abstract
526P - A phase II study of apatinib in patients with recurrent/metastatic esophageal squamous cell carcinoma (ESCC)
Presenter: Li Chu
Session: Poster display session
Resources:
Abstract
499P - Prevalence of uncommon epidermal growth factor receptor (EGFR) alterations detected by circulating tumour DNA (ctDNA) in non-small cell lung cancer (NSCLC) patients in Hong Kong
Presenter: Oscar Siu Hong Chan
Session: Poster display session
Resources:
Abstract
489P - Overall survival in patients with EGFRm+ NSCLC receiving sequential afatinib and osimertinib: Updated analysis of the GioTag study
Presenter: Maximilian J. Hochmair
Session: Poster display session
Resources:
Abstract
509P - Second-line treatment after first-line vinorelbine in advanced platinum unfit NSCLC patients: An exploratory analysis of randomized Tempo-Lung trial
Presenter: Andrea Camerini
Session: Poster display session
Resources:
Abstract
500P - Clinico-molecular characteristics of Chinese primary non-small cell lung cancer patients with compound EGFR mutations
Presenter: Jianchun Duan
Session: Poster display session
Resources:
Abstract
527P - A multicenter study of NRG1 fusions in Chinese non-small cell lung cancer patients and response to afatinib using next generation sequencing
Presenter: Xingliang Li
Session: Poster display session
Resources:
Abstract
481P - Updated survival outcomes of the phase II study of low starting dose of afatinib as first-line treatment in patients with EGFR mutation-positive non-small cell lung cancer (KTORG1402)
Presenter: Toshihide Yokoyama
Session: Poster display session
Resources:
Abstract