Management of Nonhematologic Toxicities Associated With Different EGFR-TKIs in Advanced NSCLC: A Comparison Analysis

被引:28
作者
Passaro, Antonio [1 ]
Di Maio, Massimo [2 ]
Del Signore, Ester [1 ]
Gori, Bruno [3 ]
de Marinis, Filippo [1 ]
机构
[1] IEO, Div Thorac Oncol, I-20141 Milan, Italy
[2] Fdn G Pascale IRCCS, Ist Nazl Tumori, Naples, Italy
[3] High Specializat Hosp, Oncol Pulm Unit 1, Rome, Italy
关键词
Afatinib; Diarrhea; Erlotinib; Gefitinib; Skin rash; CELL LUNG-CANCER; 1ST-LINE TREATMENT; OPEN-LABEL; PHASE-III; AFATINIB; CHEMOTHERAPY; ERLOTINIB; ADENOCARCINOMA; MULTICENTER; GEFITINIB;
D O I
10.1016/j.cllc.2014.04.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Non-hematologic toxicities are frequently observed in patients receiving epidermal growth factor receptor tyrosine kinase inhibitors in advanced non small-cell lung cancer. In this prospective research, incidence and trend of non-hematologic AEs of afatinib, erlotinib and gefitinib were compared. Results showed that safety profile of afatinib, erlotinib or gefitinib become similar after a prompt and correct management that is needed to ensure treatments without severe adverse events that could adversely affect survival and the quality of life. Introduction: Nonhematologic toxicities are frequently observed in patients receiving epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in advanced non-small-cell lung cancer (NSCLC). Materials and Methods: For the 2010-2013 period, the authors evaluated 158 patients diagnosed with advanced or metastatic NSCLC treated in first-, second-, or third-line with the EGFR-TKIs afatinib, erlotinib, or gefitinib. The study assessed the incidence of cutaneous rash, diarrhea, and mucositis/stomatitis by grade at initial assessment (< 30 days) compared with last assessment after correct management, and the authors developed a proposal for a new modality of evaluation and management of adverse events. Results: The incidence of adverse events (cutaneous rash, diarrhea, and mucositis/stomatitis), classified by grade at the initial assessment and the reevaluation after management, demonstrated a reduction of about 95% from the starting toxicity grade for diarrhea, 65% for cutaneous rash, and approximately 70% for mucositis/stomatitis. Conclusion: These results suggest that the safety profiles regarding cutaneous rash, diarrhea, and mucositis after afatinib, erlotinib, or gefitinib treatment become similar after prompt and correct management. This analysis suggests that immediate therapeutic approaches and continuous management are required to ensure treatments without severe adverse events that could adversely affect survival and the quality of life. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:307 / 312
页数:6
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