TY - JOUR
T1 - Proton pump inhibitors affect capecitabine efficacy in patients with stage II–III colorectal cancer
T2 - a multicenter retrospective study
AU - Kitazume, Yoshiko
AU - Kawazoe, Hitoshi
AU - Uozumi, Ryuji
AU - Yoshizawa, Tomoe
AU - Iihara, Hirotoshi
AU - Fujii, Hironori
AU - Takahashi, Masaya
AU - Arai, Takahiro
AU - Murachi, Yasushi
AU - Sato, Yumiko
AU - Mikami, Takahiro
AU - Hashiguchi, Koji
AU - Yamazaki, Tomoko
AU - Takahashi, Katsuyuki
AU - Fujita, Yukiyoshi
AU - Hosokawa, Yuki
AU - Morozumi, Issei
AU - Tsuchiya, Masami
AU - Yokoyama, Atsushi
AU - Hashimoto, Hironobu
AU - Yamaguchi, Masakazu
N1 - Funding Information:
This work was partly supported by the Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research in Japan (to H.K./2021/04). The funders had no role in the design of the study; collection, analysis, and interpretation of the data; writing of the manuscript; and decision to submit the manuscript for publication. We are grateful to all participants and medical staff at the nine participating institutions: National Cancer Center Hospital, Tochigi Cancer Center, Gifu University Hospital, Osaka City University Hospital, Gunma Prefectural Cancer Center, Osaka University Hospital, Nagoya City University West Medical Center, Miyagi Cancer Center, and Yokohama Minami Kyousai Hospital who were involved in this study. We would like to thank Editage ( www.editage.com ) for English language editing.
Funding Information:
The study protocol was approved by the National Cancer Center Institutional Review Board (approval number: 2019–294), ethics committee of the Tochigi Cancer Center (approval number: 20-A001), medical review board of Gifu University Graduate School of Medicine (approval number: 2020–069), ethical committee of Osaka City University Graduate School of Medicine (approval number: 2020–042), ethics committee of the Gunma Prefectural Cancer Center (approval number: 405–02,012), ethical review board of Osaka University Hospital (approval number: 20008), Nagoya City University East/West medical center Institutional Review Board (approval number: 20–04-423–03), ethics review committee of the Miyagi Cancer Center (approval number: 2020–003), and ethics committee of the Yokohama Minami Kyosai Hospital (approval number: 1–20-4–1) in Japan. This study was conducted per the Declaration of Helsinki and the Ethical Guidelines for Medical and Health Research involving Human Subjects by the Ministry of Education, Culture, Sports, Science, and Technology and the Ministry of Health, Labour, and Welfare of Japan. Informed consent was waived by the ethics committee of National Cancer Center, Tochigi Cancer Center, Gifu University Graduate School of Medicine, Osaka City University Graduate School of Medicine, Gunma Prefectural Cancer Center, Osaka University Hospital, Nagoya City University East/West medical center, Miyagi Cancer Center, and Yokohama Minami Kyosai Hospital considering retrospective nature of the study. Acknowledgements
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - The association between capecitabine efficacy and proton pump inhibitors (PPIs) is controversial. Here, we determined whether co-administration of PPIs affects the real-world effectiveness of capecitabine. This retrospective observational study included consecutive patients with stage II–III colorectal cancer (CRC) who received adjuvant capecitabine monotherapy or CapeOX (capecitabine and oxaliplatin) between January 2009 and December 2014 at nine participating institutions. The primary endpoint was the difference in relapse-free survival (RFS) between patients who received PPIs and those who did not and was estimated using the Kaplan–Meier method. Overall survival (OS) was the secondary endpoint. Multivariable analysis of RFS and OS was performed using a Cox proportional hazards model, propensity score adjustment, and inverse probability of treatment weighting (IPTW) analyses. Data from 606 patients were evaluated, 54 of whom had received a PPI. PPI-treated patients tended to have poorer RFS and OS than patients treated without PPIs. The hazard ratio for RFS with capecitabine monotherapy was 2.48 (95% confidence interval: 1.22–5.07). These results were consistent with sensitivity analyses performed using propensity score adjustment and IPTW methods. Co-administration of PPIs may reduce the effectiveness of capecitabine and negatively impact patients with stage II–III CRC.
AB - The association between capecitabine efficacy and proton pump inhibitors (PPIs) is controversial. Here, we determined whether co-administration of PPIs affects the real-world effectiveness of capecitabine. This retrospective observational study included consecutive patients with stage II–III colorectal cancer (CRC) who received adjuvant capecitabine monotherapy or CapeOX (capecitabine and oxaliplatin) between January 2009 and December 2014 at nine participating institutions. The primary endpoint was the difference in relapse-free survival (RFS) between patients who received PPIs and those who did not and was estimated using the Kaplan–Meier method. Overall survival (OS) was the secondary endpoint. Multivariable analysis of RFS and OS was performed using a Cox proportional hazards model, propensity score adjustment, and inverse probability of treatment weighting (IPTW) analyses. Data from 606 patients were evaluated, 54 of whom had received a PPI. PPI-treated patients tended to have poorer RFS and OS than patients treated without PPIs. The hazard ratio for RFS with capecitabine monotherapy was 2.48 (95% confidence interval: 1.22–5.07). These results were consistent with sensitivity analyses performed using propensity score adjustment and IPTW methods. Co-administration of PPIs may reduce the effectiveness of capecitabine and negatively impact patients with stage II–III CRC.
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U2 - 10.1038/s41598-022-10008-2
DO - 10.1038/s41598-022-10008-2
M3 - Article
C2 - 35449143
AN - SCOPUS:85128638891
SN - 2045-2322
VL - 12
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 6561
ER -