PMID- 22135121 OWN - NLM STAT- MEDLINE DCOM- 20120424 LR - 20211021 IS - 1549-490X (Electronic) IS - 1083-7159 (Print) IS - 1083-7159 (Linking) VI - 16 IP - 12 DP - 2011 TI - The outcomes and safety of single-agent sorafenib in the treatment of elderly patients with advanced hepatocellular carcinoma (HCC). PG - 1721-8 LID - 10.1634/theoncologist.2011-0192 [doi] AB - BACKGROUND: With the aging population, hepatocellular carcinoma (HCC) in the elderly represents a significant health burden. We aimed to evaluate and compare the efficacy and tolerability of single-agent sorafenib in treating elderly patients with advanced HCC versus the younger population. METHODS: We retrospectively analyzed a consecutive cohort of advanced HCC patients with Child-Pugh A or B liver function and an Eastern Cooperative Oncology Group performance status score of 0-2 treated with sorafenib. The patients were categorized into older (age >/=70 years) and younger (age <70 years) groups. Treatment outcomes and related adverse events (AEs) were compared. RESULTS: In total, 172 patients, 35 in the older (median age, 73 years) and 137 in the younger (median age, 55 years) group, were analyzed. The median progression-free survival time was similar in the older and younger groups (2.99 months versus 3.09 months; p = .275), as was the overall survival time (5.32 months versus 5.16 months; p = .310). Grade 3 or 4 AEs were observed in 68.6% of older and 62.7% of younger patients (p = .560), with neutropenia (11.4% versus 0.7%; p = .007), malaise (11.4% versus 2.2%; p = .033), and mucositis (5.7% versus 0.0%; p = .041) being more frequently reported in the elderly cohort. CONCLUSIONS: The survival benefits and overall treatment-related AEs of sorafenib are comparable in elderly and younger advanced HCC patients. Nevertheless, more vigilant monitoring in the elderly is warranted because they are more susceptible to develop neutropenia, malaise, and mucositis. FAU - Wong, Hilda AU - Wong H AD - Department of Medicine, Queen Mary Hospital, Hong Kong. FAU - Tang, Yuen Fong AU - Tang YF FAU - Yao, Tzy-Jyun AU - Yao TJ FAU - Chiu, Joanne AU - Chiu J FAU - Leung, Roland AU - Leung R FAU - Chan, Pierre AU - Chan P FAU - Cheung, Tan To AU - Cheung TT FAU - Chan, Albert C AU - Chan AC FAU - Pang, Roberta W AU - Pang RW FAU - Poon, Ronnie AU - Poon R FAU - Fan, Sheung-Tat AU - Fan ST FAU - Yau, Thomas AU - Yau T LA - eng PT - Comparative Study PT - Journal Article DEP - 20111201 PL - England TA - Oncologist JT - The oncologist JID - 9607837 RN - 0 (Antineoplastic Agents) RN - 0 (Benzenesulfonates) RN - 0 (Phenylurea Compounds) RN - 0 (Pyridines) RN - 25X51I8RD4 (Niacinamide) RN - 9ZOQ3TZI87 (Sorafenib) SB - IM MH - Adult MH - Age Factors MH - Aged MH - Antineoplastic Agents/*therapeutic use MH - Benzenesulfonates/*therapeutic use MH - Carcinoma, Hepatocellular/*drug therapy MH - Cohort Studies MH - Disease-Free Survival MH - Female MH - Humans MH - Liver Neoplasms/*drug therapy MH - Male MH - Middle Aged MH - Niacinamide/analogs & derivatives MH - Phenylurea Compounds MH - Pyridines/*therapeutic use MH - Retrospective Studies MH - Sorafenib MH - Treatment Outcome PMC - PMC3248771 COIS- Disclosures: Hilda Wong: None; Yuen Fong Tang: None; Tzy-Jyun Yao: None; Joanne Chiu: None; Roland Leung: None; Pierre Chan: None; Tan To Cheung: None; Albert C. Chan: None; Roberta W. Pang: None; Ronnie Poon: Bayer Pharmaceuticals Limited (RF); Sheung-Tat Fan: None; Thomas Yau: Bayer Schering (C/A). EDAT- 2011/12/03 06:00 MHDA- 2012/04/25 06:00 PMCR- 2012/12/01 CRDT- 2011/12/03 06:00 PHST- 2011/12/03 06:00 [entrez] PHST- 2011/12/03 06:00 [pubmed] PHST- 2012/04/25 06:00 [medline] PHST- 2012/12/01 00:00 [pmc-release] AID - theoncologist.2011-0192 [pii] AID - 3737266 [pii] AID - 10.1634/theoncologist.2011-0192 [doi] PST - ppublish SO - Oncologist. 2011;16(12):1721-8. doi: 10.1634/theoncologist.2011-0192. Epub 2011 Dec 1.