Association between proton pump inhibitor use and mortality in patients with hepatocellular carcinoma receiving tyrosine kinase inhibitor
Discontinuation was defined as a gap of more than 30 days in TKI use after the index date. Since TKI reimbursement was discontinued by Taiwan NHI in patients with disease progression, TKIs discontinuation was used as a surrogate outcome for tumour progression. IPTW adjustment resulted in less signif...
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Published in | Gut Vol. 70; no. 8; pp. 1598 - 1599 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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BMJ Publishing Group LTD
01.08.2021
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ISSN | 0017-5749 1468-3288 1468-3288 |
DOI | 10.1136/gutjnl-2020-321932 |
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Abstract | Discontinuation was defined as a gap of more than 30 days in TKI use after the index date. Since TKI reimbursement was discontinued by Taiwan NHI in patients with disease progression, TKIs discontinuation was used as a surrogate outcome for tumour progression. IPTW adjustment resulted in less significant differences in most baseline patient characteristics, comorbidities and concomitant drugs use between the PPI and non-PPI cohorts (table 1).Table 1 Demographic characteristics of the study subjects after inverse probability of treatment weighting (IPTW) adjustment Characteristics PPI Non-PPI Difference Difference n=2196 n=8013 Unadjusted Adjusted Age, years 63.664 63.638 −1.10 0.026 Male 79.9% 79.0% 0.035 0.002 Comorbidities Chronic hepatitis B 87.6% 87.8% −0.010 −0.002 Chronic hepatitis C 35.6% 36.0% −0.017 −0.004 Alcoholic liver diseases 13.1% 12.6% 0.027 0.005 Liver decompensation 20.4% 20.1% 0.098 0.003 Peptic ulcer diseases 61.3% 61.1% 0.180 0.002 Diabetes mellitus 38.4% 37.8% 0.001 0.006 Hypertension 59.3% 58.7% −0.016 0.007 Hypercholesteraemia 17.0% 16.8% −0.007 0.002 Cerebrovascular events 14.4% 14.3% −0.001 0.001 Acute coronary syndrome 23.2% 23.3% −0.005 0.000 Chronic obstructive pulmonary disease 29.3% 29.1% −0.002 0.002 Chronic renal diseases 8.7% 8.3% −0.009 0.004 Osteoporosis 2.4% 2.4% −0.004 −0.001 Bone fracture 27.7% 27.1% 0.002 −0.001 Heart failure 6.2% 6.4% 0.002 −0.002 Liver failure 7.7% 7.6% 0.017 0.002 Renal failure 13.8% 13.5% 0.000 0.003 Vascular invasion 21.0% 20.5% 0.084 0.004 Concomitant drug use Nucleos(t)ide analogue use 23.% 23.1% 0.032 −0.001 Statins use 4.1% 4.1% −0.004 0.000 Metformin use 11.4% 11.1% −0.006 0l003 Oral antibiotics use 25.7% 25.8% 0.151 −0.001 PPI, proton pump inhibitor. [...]concomitant PPI and TKI use is prevalent and associated with an increased risk of overall mortality in patients with advanced stage HCC. |
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AbstractList | Discontinuation was defined as a gap of more than 30 days in TKI use after the index date. Since TKI reimbursement was discontinued by Taiwan NHI in patients with disease progression, TKIs discontinuation was used as a surrogate outcome for tumour progression. IPTW adjustment resulted in less significant differences in most baseline patient characteristics, comorbidities and concomitant drugs use between the PPI and non-PPI cohorts (table 1).Table 1 Demographic characteristics of the study subjects after inverse probability of treatment weighting (IPTW) adjustment Characteristics PPI Non-PPI Difference Difference n=2196 n=8013 Unadjusted Adjusted Age, years 63.664 63.638 −1.10 0.026 Male 79.9% 79.0% 0.035 0.002 Comorbidities Chronic hepatitis B 87.6% 87.8% −0.010 −0.002 Chronic hepatitis C 35.6% 36.0% −0.017 −0.004 Alcoholic liver diseases 13.1% 12.6% 0.027 0.005 Liver decompensation 20.4% 20.1% 0.098 0.003 Peptic ulcer diseases 61.3% 61.1% 0.180 0.002 Diabetes mellitus 38.4% 37.8% 0.001 0.006 Hypertension 59.3% 58.7% −0.016 0.007 Hypercholesteraemia 17.0% 16.8% −0.007 0.002 Cerebrovascular events 14.4% 14.3% −0.001 0.001 Acute coronary syndrome 23.2% 23.3% −0.005 0.000 Chronic obstructive pulmonary disease 29.3% 29.1% −0.002 0.002 Chronic renal diseases 8.7% 8.3% −0.009 0.004 Osteoporosis 2.4% 2.4% −0.004 −0.001 Bone fracture 27.7% 27.1% 0.002 −0.001 Heart failure 6.2% 6.4% 0.002 −0.002 Liver failure 7.7% 7.6% 0.017 0.002 Renal failure 13.8% 13.5% 0.000 0.003 Vascular invasion 21.0% 20.5% 0.084 0.004 Concomitant drug use Nucleos(t)ide analogue use 23.% 23.1% 0.032 −0.001 Statins use 4.1% 4.1% −0.004 0.000 Metformin use 11.4% 11.1% −0.006 0l003 Oral antibiotics use 25.7% 25.8% 0.151 −0.001 PPI, proton pump inhibitor. [...]concomitant PPI and TKI use is prevalent and associated with an increased risk of overall mortality in patients with advanced stage HCC. |
Author | Wu, Chen-Yi Hsu, Yao-Chun Chen, Yi-Ju Lee, Teng-Yu Wu, Chun-Ying Ho, Hsiu J Lin, Jaw-Town |
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Cites_doi | 10.2147/CMAR.S222278 10.1001/2012.jama.11975 10.1136/gutjnl-2019-318830 10.1056/NEJMoa0708857 10.1136/gutjnl-2019-318506 10.1038/clpt.2012.73 10.1158/1078-0432.CCR-09-3033 10.1053/j.gastro.2014.03.048 10.1002/cncr.31917 |
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Copyright | Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. 2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. |
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References | Fang, Yang, Hsieh 2019; 11 Wu, Chen, Ho 2012; 308 Xu, Liu, Feng 2020; 69 Sharma, Holmes, Mehta 2019; 125 Lind, Dingemans, Groen 2010; 16 Wu, Lin, Ho 2014; 147 Llovet, Ricci, Mazzaferro 2008; 359 Wang, Wang, Lieftink 2020; 69 Budha, Frymoyer, Smelick 2012; 92 2022012403100948000_70.8.1598.6 2022012403100948000_70.8.1598.5 2022012403100948000_70.8.1598.4 2022012403100948000_70.8.1598.3 2022012403100948000_70.8.1598.2 2022012403100948000_70.8.1598.1 2022012403100948000_70.8.1598.9 2022012403100948000_70.8.1598.8 2022012403100948000_70.8.1598.7 |
References_xml | – volume: 11 start-page: 8539 year: 2019 article-title: Concurrent proton-pump inhibitors increase risk of death for lung cancer patients receiving 1st-line gefitinib treatment - a nationwide population-based study publication-title: Cancer Manag Res doi: 10.2147/CMAR.S222278 – volume: 308 start-page: 1906 year: 2012 article-title: Association between nucleoside analogues and risk of hepatitis B virus–related hepatocellular carcinoma recurrence following liver resection publication-title: JAMA doi: 10.1001/2012.jama.11975 – volume: 69 start-page: 1309 year: 2020 article-title: miR-541 potentiates the response of human hepatocellular carcinoma to sorafenib treatment by inhibiting autophagy publication-title: Gut doi: 10.1136/gutjnl-2019-318830 – volume: 359 start-page: 378 year: 2008 article-title: Sorafenib in advanced hepatocellular carcinoma publication-title: N Engl J Med doi: 10.1056/NEJMoa0708857 – volume: 69 start-page: 727 year: 2020 article-title: Cdk12 inhibition mediates DNA damage and is synergistic with sorafenib treatment in hepatocellular carcinoma publication-title: Gut doi: 10.1136/gutjnl-2019-318506 – volume: 92 start-page: 203 year: 2012 article-title: Drug absorption interactions between oral targeted anticancer agents and PPIs: is pH-dependent solubility the Achilles heel of targeted therapy? publication-title: Clin Pharmacol Ther doi: 10.1038/clpt.2012.73 – volume: 16 start-page: 3078 year: 2010 article-title: A multicenter phase II study of erlotinib and sorafenib in chemotherapy-naive patients with advanced non-small cell lung cancer publication-title: Clin Cancer Res doi: 10.1158/1078-0432.CCR-09-3033 – volume: 147 start-page: 143 year: 2014 article-title: Association of nucleos(t)ide analogue therapy with reduced risk of hepatocellular carcinoma in patients with chronic hepatitis B: a nationwide cohort study publication-title: Gastroenterology doi: 10.1053/j.gastro.2014.03.048 – volume: 125 start-page: 1155 year: 2019 article-title: The concomitant use of tyrosine kinase inhibitors and proton pump inhibitors: prevalence, predictors, and impact on survival and discontinuation of therapy in older adults with cancer publication-title: Cancer doi: 10.1002/cncr.31917 – ident: 2022012403100948000_70.8.1598.3 doi: 10.1056/NEJMoa0708857 – ident: 2022012403100948000_70.8.1598.1 doi: 10.1136/gutjnl-2019-318830 – ident: 2022012403100948000_70.8.1598.2 doi: 10.1136/gutjnl-2019-318506 – ident: 2022012403100948000_70.8.1598.8 doi: 10.1001/2012.jama.11975 – ident: 2022012403100948000_70.8.1598.4 doi: 10.1038/clpt.2012.73 – ident: 2022012403100948000_70.8.1598.5 doi: 10.1158/1078-0432.CCR-09-3033 – ident: 2022012403100948000_70.8.1598.7 doi: 10.2147/CMAR.S222278 – ident: 2022012403100948000_70.8.1598.9 doi: 10.1053/j.gastro.2014.03.048 – ident: 2022012403100948000_70.8.1598.6 doi: 10.1002/cncr.31917 |
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Snippet | Discontinuation was defined as a gap of more than 30 days in TKI use after the index date. Since TKI reimbursement was discontinued by Taiwan NHI in patients... |
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SubjectTerms | Antibiotics Cancer therapies Chronic obstructive pulmonary disease Congestive heart failure Diabetes mellitus Hepatitis B Hepatitis C Hepatocellular carcinoma Liver cancer Liver diseases Lung cancer Lung diseases Metformin Mortality Obstructive lung disease Osteoporosis Patients Peptic ulcers Proton pump inhibitors Renal failure Statins Tumors Tyrosine kinase inhibitors |
Title | Association between proton pump inhibitor use and mortality in patients with hepatocellular carcinoma receiving tyrosine kinase inhibitor |
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