{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,6]],"date-time":"2026-05-06T10:14:59Z","timestamp":1778062499619,"version":"3.51.4"},"reference-count":23,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2019,10,21]],"date-time":"2019-10-21T00:00:00Z","timestamp":1571616000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Thoracic Cancer"],"published-print":{"date-parts":[[2019,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>It has been reported that 20% of lung cancer patients have renal impairment caused by chronic kidney disease (CKD). Since docetaxel is predominantly excreted by the hepatobiliary system, it is administered to non\u2010small cell lung cancer (NSCLC) patients with renal impairment. However, few clinical data are available on the toxicity and efficacy of docetaxel for patients with nondialysis renal impairment. Furthermore, some cases of tubular nephrotoxicity caused by docetaxel in NSCLC patients have been reported. Therefore, a retrospective cohort study was conducted to assess the influence of nondialysis CKD on the toxicity and efficacy of docetaxel in NSCLC patients.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>NSCLC patients who received docetaxel were assessed for renal function, occurrence of adverse events and treatment efficacy.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>A total of 34 NSCLC patients who received docetaxel were studied. Eight (23.5%) patients had nondialysis CKD stage 3b or higher, with an estimated glomerular filtration rate (eGFR) &lt;45\u2009mL\/min\/1.73\u2009m<jats:sup>2<\/jats:sup>. Although the differences were not statistically significant, the starting dose of docetaxel (mg\/m<jats:sup>2<\/jats:sup>) was lower (60\u2009mg\/m<jats:sup>2<\/jats:sup>; 37.5% vs. 69.2%) in patients with an eGFR &lt;45 than that in patients with an eGFR \u226545. No significant association was observed between pretreatment eGFR and hematological and nonhematological toxicities. No significant difference was observed in the disease control rate (62.5% vs. 65.4%, <jats:italic>P<\/jats:italic> = 1.000) or in the median overall survival (10.7 vs. 11.7, <jats:italic>P<\/jats:italic> = 0.735) between patients with an eGFR &lt;45 and those with an eGFR \u226545.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Docetaxel is a reasonable option for NSCLC patients with nondialysis CKD stage 3b or higher. Dose reduction of docetaxel is also a possibility for NSCLC patients with CKD stage 3b or higher.<\/jats:p><\/jats:sec>","DOI":"10.1111\/1759-7714.13222","type":"journal-article","created":{"date-parts":[[2019,10,21]],"date-time":"2019-10-21T08:54:51Z","timestamp":1571648091000},"page":"2282-2288","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Retrospective cohort study on the safety and efficacy of docetaxel in Japanese non\u2010small cell lung cancer patients with nondialysis chronic kidney disease stage 3b or higher"],"prefix":"10.1111","volume":"10","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4600-7465","authenticated-orcid":false,"given":"Satoshi","family":"Anai","sequence":"first","affiliation":[{"name":"Department of Respiratory Medicine Harasanshin Hospital  Fukuoka 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