PMID- 30573970 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220330 IS - 1178-6930 (Print) IS - 1178-6930 (Electronic) IS - 1178-6930 (Linking) VI - 11 DP - 2018 TI - Afatinib vs erlotinib for second-line treatment of Chinese patients with advanced squamous cell carcinoma of the lung. PG - 8565-8573 LID - 10.2147/OTT.S161506 [doi] AB - BACKGROUND: The global Phase III LUX-Lung 8 trial (ClinicalTrials.gov: NCT01523587) identified significant improvements in progression-free survival (PFS), overall survival (OS), and patient-reported outcomes (PROs) with second-line afatinib vs erlotinib in patients with advanced squamous cell carcinoma (SCC) of the lung. MATERIALS AND METHODS: We conducted a post hoc analysis of data for patients in LUX-Lung 8 from mainland China (n=67). Compared with erlotinib, afatinib reduced the risk of disease progression or death (PFS) in the Chinese subgroup by 30% (HR=0.70; 95% CI: 0.38-1.27). RESULTS: The risk of death was reduced by 31% (HR=0.69; 95% CI: 0.39-1.21). The proportion of Chinese patients with improvements in PROs also favored afatinib vs erlotinib (global health status/quality of life [QoL], 52.8% vs 29.6%, P=0.072; dyspnea, 47% vs 26%, P=0.091; "dyspnea walked", 44% vs 15%, P=0.017; QoL rate, 53% vs 26%, P=0.037). DISCUSSION: While this analysis was not powered to demonstrate differences compared to the overall trial population (OTP), and there were some differences in baseline characteristics (eg, the proportion of patients aged >/=65 years old), the benefits of afatinib treatment in Chinese patients with SCC of the lung appeared to be at least comparable to that observed in LUX-Lung 8. As with the OTP, the most common adverse events (AEs) with afatinib in the Chinese subgroup were diarrhea and rash/acne, and the incidence and type of the most frequently occurring AEs were similar. CONCLUSION: The results suggest that afatinib represents a feasible treatment option for Chinese patients with advanced SCC of the lung following progression on platinum-based chemotherapy. FAU - Lu, Shun AU - Lu S AD - Shanghai Lung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China, shun_lu@hotmail.com. FAU - Li, Wei AU - Li W AD - Cancer Center, First Hospital of Jilin University, Changchun, China. FAU - Zhou, Caicun AU - Zhou C AD - Department of Oncology, Shanghai Pulmonary Hospital, Shanghai, China. FAU - Hu, Cheng-Ping AU - Hu CP AD - Department of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Qin, Shukui AU - Qin S AD - People's Liberation Army Cancer Center, Nanjing Bayi Hospital, Nanjing, Jiangsu, China. FAU - Cheng, Gang AU - Cheng G AD - Department of Medical Oncology, Beijing Hospital, National Center of Gerontology, Beijing, China. FAU - Feng, Jifeng AU - Feng J AD - Department of Internal Medicine, Jiangsu Provincial Tumor Hospital, Nanjing, China. FAU - Wang, Jie AU - Wang J AD - Department of Internal Medicine, Capital Medical University, Beijing, China. AD - Peking University School of Oncology, Beijing Cancer Hospital, Beijing, China. FAU - Cseh, Agnieszka AU - Cseh A AD - Department of Medical Affairs, Boehringer Ingelheim RCV GmbH & Co. KG, Vienna, Austria. FAU - Peil, Barbara AU - Peil B AD - Biostatistics, Boehringer Ingelheim Pharma GmbH & Co. KG. Ingelheim, Germany. FAU - Gibson, Neil AU - Gibson N AD - Translational Medicine and Clinical Oncology, Boehringer Ingelheim Pharma GmbH & Co. KG. Biberach, Germany. FAU - Ehrnrooth, Eva AU - Ehrnrooth E AD - Division of Oncology, Boehringer Ingelheim, Danmark A/S, Copenhagen, Denmark. FAU - Zhang, Li AU - Zhang L AD - Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, China. LA - eng SI - ClinicalTrials.gov/NCT01523587 PT - Journal Article DEP - 20181130 PL - New Zealand TA - Onco Targets Ther JT - OncoTargets and therapy JID - 101514322 PMC - PMC6292388 OTO - NOTNLM OT - Chinese patients OT - NSCLC OT - Phase III OT - afatinib OT - second-line OT - squamous cell carcinoma COIS- Disclosure CZ reports lecture fees from AstraZeneca, Boehringer Ingelheim, Eli Lilly, Roche, and Sanofi. AC, BP, NG, and EE report employment by Boehringer Ingelheim. The authors report no other conflicts of interest in this work. EDAT- 2018/12/24 06:00 MHDA- 2018/12/24 06:01 PMCR- 2018/11/30 CRDT- 2018/12/22 06:00 PHST- 2018/12/22 06:00 [entrez] PHST- 2018/12/24 06:00 [pubmed] PHST- 2018/12/24 06:01 [medline] PHST- 2018/11/30 00:00 [pmc-release] AID - ott-11-8565 [pii] AID - 10.2147/OTT.S161506 [doi] PST - epublish SO - Onco Targets Ther. 2018 Nov 30;11:8565-8573. doi: 10.2147/OTT.S161506. eCollection 2018.