PT - JOURNAL ARTICLE AU - MIHO TAKEMURA AU - KENJI IKEMURA AU - TETSUHIRO YOSHINAMI AU - YUJI TOYOZUMI AU - TAKUYA SHINTANI AU - MIKIKO UEDA AU - KENZO SHIMAZU AU - MASAHIRO OKUDA TI - Proton Pump Inhibitors Ameliorate Capecitabine-induced Hand-Foot Syndrome in Patients With Breast Cancer: A Retrospective Study AID - 10.21873/anticanres.15737 DP - 2022 May 01 TA - Anticancer Research PG - 2591--2598 VI - 42 IP - 5 4099 - http://ar.iiarjournals.org/content/42/5/2591.short 4100 - http://ar.iiarjournals.org/content/42/5/2591.full SO - Anticancer Res2022 May 01; 42 AB - Background/Aim: Hand-foot syndrome (HFS) is the most common adverse event associated with capecitabine, and its pathogenesis is known to be associated with inflammation. Proton pump inhibitors (PPIs) reportedly exert anti-inflammatory effects; however, the impact of PPIs on capecitabine-induced HFS needs to be clarified in the clinical setting. In the present study, we retrospectively investigated the efficacy and safety of PPIs in patients with breast cancer receiving capecitabine. Patients and Methods: We analyzed the effects of PPIs on the development of severe HFS (grade ≥2), progression-free survival (PFS), and overall survival (OS) in 195 patients who received capecitabine chemotherapy for breast cancer. Results: In total, 50 patients (26%) were treated with PPIs, while 145 patients (74%) did not receive PPIs. The incidence of severe HFS was significantly lower in patients who received PPIs (18%) than in patients who did not receive PPIs (43%, p=0.001), and the discontinuation rate of capecitabine therapy due to HFS was also lower in patients receiving PPIs than in those who did not receive PPIs (p=0.003). Multivariate analysis revealed that concomitant PPIs use was an independent factor that significantly contributed to the prevention of severe HFS (odds ratio (OR)=0.265, p=0.003). Meanwhile, no significant difference in median PFS and OS values was observed between patients treated with and without PPIs. Conclusion: Concomitant use of PPIs could ameliorate capecitabine-induced HFS in patients with breast cancer.