EGFR Mutation-positive Lung Cancer in Real-world Treatment Outcomes: A Multicenter Study from Thailand

S. Sukauichai, Kulthida Maneenil, A. Supavavej, Vinai Paul, Duangnapa Benjawongsathien, C. Chantharakhit, S. Neesanun, C. Chayangsu, Thissawan Bowornkitiwong, N. Sukaraphat
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引用次数: 5

Abstract

Background: Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI) have been the standard of care as first-line (1L) therapy for patients with advanced EGFR mutated lung cancer since 2009. In Thailand, however, it was not fully introduced to all health care funds until 2020. The purpose of this study was to determine the overall survival (OS) and treatment pattern in the period before EGFR-TKI became universally available to all patients. Methods: This was a retrospective study conducted at 10 medical centers in Thailand. Patients harboring the common mutation (exon 19 deletion or exon 21 L858R) diagnosed during January 2013 and December 2019 were enrolled. Results: This study included 284 patients with a median follow-up time of 19.8 months and a death rate of 80.3% (228/284). Clinical characteristics included median age 62.5 years, female 65.5%, never-smoking 74.3%, stage 3B/4/recurrence 2.1/93.3/4.6%, exon 19/exon 21- 60.9/38.7%. Treatment patterns to EGFR-TKI included not receiving (NR) (9.5%), first-line (1L) (56.0%), switch maintenance (MN) (3.5%), second-line (2L) (21.8%) and third-line (3L) or more (9.2%). Median OS of patient receiving EGFR-TKI as NR, 1L+MN, 2L and 3L or more was 11.10 (95%CI: 8.21 to14.00), 19.08 (95%CI: 15.76 to 22.41), 23.06 (95%CI: 15.91 to 30.21) and 32.46 (95%CI: 21.61 to 43.30) months (p=0.006), respectively. Factors contributing to poor prognosis in the multivariate model included poor ECOG-PS (HR 3.17, 95%CI: 1.96-5.13), not receiving EGFR-TKI (HR 3.83, 95%CI, 1.94-7.56) and receiving EGFR-TKI 1L (HR 2.30, 95%CI: 1.40-3.79) Conclusion: OS of patients with EGFR mutation positive lung cancer treated with EGFR-TKIs in Thailand was comparable to clinical studies. EGFR-TKI treatment should be provided to patients as early as possible, but TKI remained beneficial at later points in the treatment timeline. 
EGFR突变阳性肺癌在现实世界的治疗结果:一项来自泰国的多中心研究
背景:表皮生长因子受体酪氨酸激酶抑制剂(EGFR- tki)自2009年以来一直是晚期EGFR突变肺癌患者的一线(1L)治疗标准。然而,在泰国,直到2020年才将其全面引入所有保健基金。本研究的目的是确定EGFR-TKI普遍适用于所有患者之前的总生存期(OS)和治疗模式。方法:在泰国10个医疗中心进行回顾性研究。在2013年1月至2019年12月期间诊断出携带常见突变(外显子19缺失或外显子21 L858R)的患者入组。结果:284例患者,中位随访时间19.8个月,死亡率80.3%(228/284)。临床特征:中位年龄62.5岁,女性65.5%,从不吸烟74.3%,3B/4期/复发2.1/93.3/4.6%,外显子19/外显子21- 60.9/38.7%。EGFR-TKI的治疗模式包括不接受治疗(NR)(9.5%)、一线(1L)(56.0%)、切换维护(MN)(3.5%)、二线(2L)(21.8%)和三线(3L)或更多(9.2%)。接受EGFR-TKI治疗的NR、1L+MN、2L和3L及以上患者的中位OS分别为11.10 (95%CI: 8.21 ~ 14.00)、19.08 (95%CI: 15.76 ~ 22.41)、23.06 (95%CI: 15.91 ~ 30.21)和32.46 (95%CI: 21.61 ~ 43.30)个月(p=0.006)。在多因素模型中导致预后不良的因素包括ECOG-PS差(HR 3.17, 95%CI: 1.96-5.13)、未接受EGFR- tki (HR 3.83, 95%CI: 1.94-7.56)和接受EGFR- tki 1L (HR 2.30, 95%CI: 1.40-3.79)。结论:泰国EGFR突变阳性肺癌患者接受EGFR- tki治疗的OS与临床研究相当。应尽早向患者提供EGFR-TKI治疗,但TKI在治疗时间的后期仍然有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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