[1] NCCN. Clinical Practice Guidelines in Oncology. 2019, V5, NSCL-17.
[2] Lee, C.K.; Brown, C.; Gralla, R.J.; Hirsh, V.; Thongprasert, S.; Tsai, C.M.; Tan, E.H.; Ho, J.C.; Chu, D.T.; Zaatar, A.; Osorio Sanchez, J.A.; Vu, V.V.; Au, J.S.; Inoue, A.; Lee, S.M.; Gebski, V.; Yang, J.C. Impact of EGFR inhibitor in non-small cell lung cancer on progression-free and overall survival: a meta-analysis. J. Natl. Cancer Inst. 2013, 105, 595-605.
[3] Fukuoka, M.; Wu, Y.L.; Thongprasert, S.; Sunpaweravong, P.; Leong, S.S.; Sriuranpong, V.; Chao, T.Y.; Nakagawa, K.; Chu, D.T.; Saijo, N.; Duffield, E.L.; Rukazenkov, Y.; Speake, G.; Jiang, H.Y.; Armour, A.A.; To, K.F.; Yang, J.C.; Mok, T.S. Biomarker analyses and final overall survival results from a phase III, randomized, open-label, first-line study of gefitinib versus carboplatin/paclitaxel in clinically selected patients with advanced non-small-cell lung cancer in Asia (IPASS). J. Clin. Oncol. 2011, 29, 2866-2874.
[4] Mok, T.S.; Wu, Y.L.; Thongprasert, S.; Yang, C.H.; Chu, D.T.; Saijo, N.; Sunpaweravong, P.; Han, B.H.; Margono, B.; Ichinose, Y.; Nishiwaki, Y.; Ohe, Y.; Yang, J.J.; Chewaskulyong, B.; Jiang, H.Y.; Duffield, E.L.; Watkins, C.L.; Armour, A.A.; Fukuoka, M. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N. Engl. J. Med. 2009, 361, 947-957.
[5] Kumarakulasinghe, N.B.; van Zanwijk, N.; Soo, R.A. Molecular targeted therapy in the treatment of advanced stage non-small cell lung cancer (NSCLC). Respirol. 2015, 20, 370-378.
[6] Mitsudomi, T.; Morita, S.; Yatabe, Y.; Negoro, S.; Okamoto, I.; Tsurutani, J.; Seto, T.; Satouchi, M.; Tada, H.; Hirashima, T.; Asami, K.; Katakami, N.; Takada, M.; Yoshioka, H.; Shibata, K.; Kudoh, S.; Shimizu, E.; Saito, H.; Toyooka, S.; Nakagawa, K.; Fukuoka, M.; West Japan Oncology Group. Gefitinib versus cisplatin plus docetaxel in patients with non-small-cell lung cancer harbouring mutations of the epidermal growth factor receptor (WJTOG3405): an open label, randomised phase 3 trial. Lancet Oncol. 2010, 11, 121-128.
[7] EMA. European Medicines Agency. 2009, 11-21.
[8] Tang, W.F.; Tomkinson, H.; Masson, E. Effect of sustained elevated gastric pH levels on gefitinib exposure. Clin. Pharmacol. Drug Dev. 2017, 6, 517-523.
[9] Yasumuro, O.; Uchida, S.; Kashiwagura, Y.; Suzuki, A.; Tanaka, S.; Inui, N.; Watanabe, H.; Namiki, N. Changes in gefitinib, erlotinib and osimertinib pharmacokinetics under various gastric pH levels following oral administration of omeprazole and vonoprazan in rats. Xenobiotica. 2018, 48, 1106-1112.
[10] Yokota, H.; Sato, K.; Okuda, Y.; Kobayashi, H.; Takeda, M.; Asano, M.; Ito, H.; Miura, M. Effects of histamine 2-receptor antagonists and proton pump inhibitors on the pharmacokinetics of gefitinib in patients with non-small-cell lung cancer. Clin. Lung Cancer. 2017, 18, e433-e439.
[11] Reid, M.; Keniston, A.; Heller, J.C.; Miller, M.; Medvedev, S.; Albert, R.K. Inappropriate prescribing of proton pump inhibitors in hospitalized patients. J. Hosp. Med. 2012, 7, 421-425.
[12] Guda, N.M.; Noonan, M.; Kreiner, M.J.; Partington, S.; Vakil, N. Use of intravenous proton pump inhibitors in community practice: an explanation for the shortage? Am. J. Gastroenterol. 2004, 99, 1233-1237.
[13] Ying, J.; Li, L.C.; Wu, C.Y.; Yu Z.W.; Kan L.D. The status of proton pump inhibitor use: a prescription survey of 45 hospitals in China. Rev. Esp. Enferm. Dig. 2019, 111, 738-743.
[14] Hoover, J.G.; Schumaker, A.L.; Franklin, K.J. Use of intravenous proton-pump inhibitors in a teaching hospital practice. Dig. Dis. Sci. 2009, 54, 1947-1952.
[15] Tasaka, C.L.; Burg, C.; VanOsdol, S.J.; Bekeart, L.; Anglemyer, A.; Tsourounis, C.; Rennke, S. An interprofessional approach to reducing the overutilization of stress ulcer prophylaxis in adult medical and surgical intensive care units. Ann. Pharmacother. 2014, 48, 462-469.
[16] Zenke, Y.; Yoh, K.; Matsumoto, S.; Umemura, S.; Niho, S.; Ohmatsu, H.; Goto, K.; Ohe, Y. Clinical impact of gastric acid-suppressing medication use on the efficacy of erlotinib and gefitinib in patients with advanced non-small-cell lung cancer harboring EGFR mutations. Clin. Lung Cancer. 2016, 17, 412-418.
[17] Kumarakulasinghe, N.B.; Syn, N.; Soon, Y.Y.; Asmat, A.; Zheng, H.L.; Loy, E.Y.; Pang, B.; Soo, R.A. EGFR kinase inhibitors and gastric acid suppressants in EGFR-mutant NSCLC: a retrospective database analysis of potential drug interaction. Oncotarget. 2016, 7, 85542-85550.
[18] Chu, M.P.; Ghosh, S.; Chambers, C.R.; Basappa, N.; Butts, C.A.; Chu, Q.; Fenton, D.; Joy, A.A.; Sangha, R.; Smylie, M.; Sawyer, M.B. Gastric Acid suppression is associated with decreased erlotinib efficacy in non-small-cell lung cancer. Clin. Lung Cancer. 2015, 16, 33-39.
[19] Forsythe, B.; Faulkner, K. Overview of the tolerability of gefitinib (Iressa) monotherapy: clinical experience in non-small-cell lung cancer. Drug Saf. 2004, 27, 1081-1092.
[20] Hsiue, E.H.; Lee, J.H.; Lin, C.C.; Yang, J.C. Safety of gefitinib in non-small cell lung cancer treatment. Expert Opin. Drug Saf. 2016, 15, 993-1000. |