PMID- 25276283 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20141003 LR - 20220310 IS - 1948-5182 (Print) IS - 1948-5182 (Electronic) VI - 6 IP - 9 DP - 2014 Sep 27 TI - Skin toxicity predicts efficacy to sorafenib in patients with advanced hepatocellular carcinoma. PG - 670-6 LID - 10.4254/wjh.v6.i9.670 [doi] AB - AIM: To study the relationship between adverse events (AEs), efficacy, and nursing intervention for sorafenib therapy in patients with hepatocellular carcinoma (HCC). METHODS: We enrolled 37 consecutive patients with advanced HCC who received sorafenib therapy. Relationships among baseline characteristics as well as AE occurrence and tumor response, overall survival (OS), and treatment duration were analyzed. The nursing intervention program consisted of education regarding self-monitoring and AEs management, and telephone follow-up was provided once in 1-2 wk. RESULTS: A total of 37 patients were enrolled in the study, comprising 30 males (81%) with a median age of 71 years. The disease control rate at 3 mo was 41%, and the median OS and treatment duration were 259 and 108 d, respectively. Nursing intervention was given to 24 patients (65%). Every patient exhibited some kinds of AEs, but no patients experienced G4 AEs. Frequently observed AEs > G2 included anorexia (57%), skin toxicity (57%), and fatigue (54%). Factors significantly associated with longer OS in multivariate analysis demonstrated that age G2 skin toxicity, and absence of > G2 hypoalbuminemia. The disease control rate in patients with > G2 skin toxicity was 13/20 (65%), which was significantly higher compared with that in patients with no or G1 skin toxicity. Multivariate analysis revealed that nursing intervention and > G2 skin toxicity were independent significant predictors for longer treatment duration. CONCLUSION: Skin toxicity was associated with favorable outcomes with sorafenib therapy for advanced HCC. Nursing intervention contributed to better adherence, which may improve the efficacy of sorafenib. FAU - Shomura, Masako AU - Shomura M AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. FAU - Kagawa, Tatehiro AU - Kagawa T AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. FAU - Shiraishi, Koichi AU - Shiraishi K AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. FAU - Hirose, Shunji AU - Hirose S AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. FAU - Arase, Yoshitaka AU - Arase Y AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. FAU - Koizumi, Jun AU - Koizumi J AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. FAU - Mine, Tetsuya AU - Mine T AD - Masako Shomura, Department of Nursing, Tokai University School of Health Sciences, Isehara, Kanagawa 2591193, Japan. LA - eng PT - Journal Article PL - United States TA - World J Hepatol JT - World journal of hepatology JID - 101532469 PMC - PMC4179146 OTO - NOTNLM OT - Drug toxicity OT - Hepatocellular carcinoma OT - Molecular targeted therapy OT - Nursing intervention OT - Surrogate marker EDAT- 2014/10/03 06:00 MHDA- 2014/10/03 06:01 PMCR- 2014/09/27 CRDT- 2014/10/03 06:00 PHST- 2014/05/16 00:00 [received] PHST- 2014/07/16 00:00 [revised] PHST- 2014/08/27 00:00 [accepted] PHST- 2014/10/03 06:00 [entrez] PHST- 2014/10/03 06:00 [pubmed] PHST- 2014/10/03 06:01 [medline] PHST- 2014/09/27 00:00 [pmc-release] AID - 10.4254/wjh.v6.i9.670 [doi] PST - ppublish SO - World J Hepatol. 2014 Sep 27;6(9):670-6. doi: 10.4254/wjh.v6.i9.670.