Clinical characteristics of non-small cell lung cancer patients who experienced acquired resistance during gefitinib treatment

被引:20
作者
Kim, Hye-Ryoun [1 ]
Lee, Jae Chol [2 ]
Kim, Young-Chul [3 ]
Kim, Kyu-Sik [3 ]
Oh, In-Jae [3 ]
Lee, Sung Yong [4 ]
Jang, Tae Won [5 ]
Lee, Min Ki [6 ]
Shin, Kyeong-Cheol [7 ]
Lee, Gwan Ho [7 ]
Ryu, Jeong-Seon [8 ]
Jang, Seung Hoon [9 ]
Son, Ji Woong [10 ]
Lee, Jeong Eun [11 ]
Kim, Sun Young [11 ]
Kim, Hee Joung [12 ]
Lee, Kye Young [12 ]
机构
[1] Korea Canc Ctr Hosp, Dept Internal Med, Seoul 139706, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul, South Korea
[3] Chonnam Natl Univ, Coll Med, Hwasun Hosp, Dept Internal Med, Hwasun, South Korea
[4] Korea Univ, Coll Med, Dept Internal Med, Guro Hosp, Seoul 136705, South Korea
[5] Kosin Univ, Coll Med, Dept Internal Med, Pusan, South Korea
[6] Pusan Natl Univ, Coll Med, Dept Internal Med, Pusan 609735, South Korea
[7] Yeungnam Univ, Coll Med, Dept Internal Med, Taegu, South Korea
[8] Inha Univ, Coll Med, Dept Internal Med, Inchon, South Korea
[9] Hallym Univ, Coll Med, Dept Internal Med, Anyang, South Korea
[10] Konyang Univ, Coll Med, Dept Internal Med, Taejon, South Korea
[11] Chungnam Natl Univ, Coll Med, Dept Internal Med, Taejon, South Korea
[12] Konkuk Univ, Coll Med, Dept Internal Med, Seoul 143729, South Korea
关键词
Acquired resistance; Gefitinib; EGFR-tyrosine kinase inhibitor; Non-small cell lung cancer; Post-progression survival (PPS); Failure togefitinib; GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITOR; PREVIOUSLY TREATED PATIENTS; T790M MUTATIONS; CHEMOTHERAPY; CARBOPLATIN; PACLITAXEL; FAILURE; TRIAL; PLUS;
D O I
10.1016/j.lungcan.2013.11.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The NSCLC patients who experienced good clinical responses to an EGFR-TKI will inevitably develop acquired resistance. A great deal of research is being carried out to discover the molecular mechanisms underlying this resistance. In comparison, few studies have been conducted to find out about the clinical characteristics of acquired resistance in the patients who had responded to an EGFR-TKI. Herein we investigated clinical characteristics of NSCLC patients who experienced acquired resistance during gefitinib therapy. Patients and methods: We reviewed NSCLC patients who showed a clinical benefit from initial gefitinib therapy. All clinical data were obtained from 11 centers of Korean Molecular Lung Cancer Group (KMLCG). The clinical manifestations of acquired resistance, time to progression (TTP), and post-progression survival (PPS) after gefitinib failure were analyzed retrospectively. Results: A total of 417 patients were recruited. Median TTP was 10.2 months (95% CI, 9.5-10.9). TTP showed a significant longer duration in female, non-smoker, and patients with adenocarcinoma. At the time of acquired resistance, 63.3% of the patients showed symptomatic deterioration. Sites of disease progression were as follows: primary lung lesion in 58.4%, previous metastasis in 38.3%, and new metastasis in 54.2%. Patients with EGFR wild type showed a tendency of higher frequency in symptomatic deterioration and newly development of CNS metastasis compared with patients with EGFR mutation. There was a significant difference in newly development of lung metastasis between patients with exon 19 deletion and those with L858R mutation (41.4% vs. 6.3%, p = 0.02). PPS was 8.9 months (95% CI, 7.4-10.4). Smoking history, PS, new CNS lesion and subsequent chemotherapy were independent factors for PPS. Conclusion: This study suggests that clinical manifestations of acquired resistance may be different according to EGFR mutation status and EGFR mutation genotype. In addition, subsequent chemotherapy confers clinical benefit in terms of PPS in NSCLC patients who experienced acquired resistance after gefitinib therapy. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:252 / 258
页数:7
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