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Microwave ablation with continued EGFR tyrosine kinase inhibitor therapy prolongs disease control in non‐small‐cell lung cancers with acquired resistance to EGFR tyrosine kinase inhibitors

机译:微波消融和持续的EGFR酪氨酸激酶抑制剂治疗可延长对EGFR酪氨酸激酶抑制剂具有耐药性的非小细胞肺癌的疾病控制

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Background Although patients with EGFR ‐mutant non‐small‐cell lung cancer (NSCLC) benefit from treatment with EGFR‐tyrosine kinase inhibitors (TKIs), outcomes are limited by the eventual development of acquired resistance. We conducted a retrospective study to evaluate the efficacy and feasibility of EGFR‐TKI therapy beyond focal progression, associated with microwave ablation. Methods Patients with metastatic EGFR ‐mutant NSCLC treated with EGFR‐TKIs at our institutions from May 2012 to December 2017 were identified. Patients with single lesion progression, treated with MWA, and continually administered EGFR‐TKI therapy until further progression, were included in the study. Initial response to target therapy, median progression‐free survival (PFS1), and first progression site were recorded. The median time to progression after local therapy (PFS2) was also assessed. Overall survival was calculated from the initiation of EGFR‐TKIs to the date of final follow‐up or death. Results Fifteen out of 205 patients (10%) satisfied the inclusion criteria. Local therapy was well tolerated, and complete ablation was performed in 11 (73.3%) patients. The median PFS1 was 9.5 months (range 6–41), and the median PFS2 was 8 months (range 3–24). The corresponding 6 and 12 month PFS rates were 73.3% and 26.7%, respectively. Median overall survival was 23 months (range 15–64). Conclusion The longer disease control observed in our patients suggests that continuation of EGFR‐TKI beyond focal progression associated to microwave ablation is an efficacious therapeutic strategy.
机译:背景技术尽管患有EGFR突变的非小细胞肺癌(NSCLC)的患者受益于EGFR酪氨酸激酶抑制剂(TKIs)的治疗,但结局受限于最终获得性耐药的发展。我们进行了一项回顾性研究,以评估EGFR‐TKI治疗与局灶性进展,微波消融相关的疗效和可行性。方法确定2012年5月至2017年12月在我们机构接受EGFR-TKIs治疗的转移性EGFR突变NSCLC患者。研究纳入了单病灶进展,接受MWA治疗并持续进行EGFR-TKI治疗直至进一步进展的患者。记录对靶标治疗的初始反应,中位无进展生存期(PFS1)和第一个进展部位。还评估了局部治疗后进展的中位时间(PFS2)。从启动EGFR-TKIs到最终随访或死亡之日计算总生存期。结果205名患者中有15名(10%)符合纳入标准。局部治疗耐受良好,对11例(73.3%)的患者进行了完全消融。 PFS1的中位数为9.5个月(范围6–41),PFS2的中位数为8个月(范围3–24)。相应的6个月和12个月PFS率分别为73.3%和26.7%。中位总生存期为23个月(范围15-64)。结论在我们的患者中观察到的更长的疾病控制表明EGFR-TKI的持续发展超过了与微波消融相关的局灶性进展是一种有效的治疗策略。

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