首页> 外文期刊>Medicine. >Local microwave ablation with continued EGFR tyrosine kinase inhibitor as a treatment strategy in advanced non-small cell lung cancers that developed extra-central nervous system oligoprogressive disease during EGFR tyrosine kinase inhibitor treatment: A pilot study
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Local microwave ablation with continued EGFR tyrosine kinase inhibitor as a treatment strategy in advanced non-small cell lung cancers that developed extra-central nervous system oligoprogressive disease during EGFR tyrosine kinase inhibitor treatment: A pilot study

机译:EGFR酪氨酸激酶抑制剂的局部微波消融作为晚期非小细胞肺癌的治疗策略,该晚期非小细胞肺癌在EGFR酪氨酸激酶抑制剂的治疗过程中发展为中枢神经系统寡聚进展性疾病:一项先导研究

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The non-small cell lung cancer (NSCLC) patients that experienced good clinical response to epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKIs) will ultimately develop acquired resistance. This retrospective study was performed to explore the potential survival benefit of microwave ablation (MWA) therapy in epidermal growth factor receptor (EGFR)-mutant NSCLC that developed extra-central nervous system (CNS) oligoprogressive disease during TKI treatment.We retrospectively analyzed 54 NSCLC patients with EGFR mutations who showed a clinical benefit from initial EGFR-TKI therapy and developed extra-CNS oligoprogressive disease at our institutions. Twenty eight patients received MWA as a local therapy for the metastatic sites and continued on the same TKIs (MWA group). The following 26 patients received systemic chemotherapy after progression (chemotherapy group). The progression-free survival (PFS1) was calculated from initiation of targeted therapy to first progression. Progression-free survival (PFS2) was defined from first progression to second progression after MWA or chemotherapy. Overall survival (OS) was calculated from the time of diagnosis to the date of last follow-up or death.The median PFS1 for both groups was similar (median 12.6 vs. 12.9 months, HR 0.63). However, the MWA group patients had a significantly longer PFS2 (median 8.8 vs. 5.8 months, hazards ratio [HR] 0.357) and better OS (median 27.7 vs. 20.0, HR 0.238) in comparison with chemotherapy group. Multivariate analysis and the internal validation identified MWA as the main favorable prognostic factor for PFS2 and OS. In the MWA group, the median PFS2 for complete ablation was significantly longer than that for incomplete ablation (11 vs. 4.2 months, HR 0.29, P<0.05).MWA with continued EGFR inhibition might be associated with favorable progression-free survival (PFS) and OS in patients with extra-CNS oligometastatic disease. MWA as a local therapy for extra-CNS oligometastatic disease should be considered for NSCLC with acquired resistance to EGFR-TKIs.
机译:对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)表现出良好临床反应的非小细胞肺癌(NSCLC)患者最终将获得获得性耐药。这项回顾性研究旨在探讨微波消融(MWA)治疗在TKI治疗期间发展为中枢神经系统(CNS)少进展性疾病的表皮生长因子受体(EGFR)突变型非小细胞肺癌的潜在生存益处。我们回顾性分析了54种非小细胞肺癌。具有EGFR突变的患者,这些患者在最初的EGFR-TKI治疗中显示出临床获益,并且在我们的机构中​​发生了CNS少进展性疾病。二十八名患者接受MWA作为转移部位的局部治疗,并继续在相同的TKI(MWA组)上治疗。以下26名患者在病情恶化后接受了全身化学疗法(化学疗法组)。无进展生存期(PFS1)是从靶向治疗开始到首次进展计算的。无进展生存期(PFS2)定义为MWA或化疗后从第一次进展到第二次进展。从诊断到最后一次随访或死亡之日计算总生存期(OS),两组的中位PFS1相似(中位数12.6 vs.12.9个月,HR 0.63)。然而,与化疗组相比,MWA组患者的PFS2明显更长(中位8.8 vs. 5.8个月,危险比[HR] 0.357)和OS更好(中位27.7 vs. 20.0,HR 0.238)。多变量分析和内部验证确定MWA是PFS2和OS的主要有利预后因素。在MWA组中,完全消融的中位PFS2显着长于不完全消融的中位(11 vs.4.2个月,HR 0.29,P <0.05).MWA持续受到EGFR抑制可能与无进展生存期相关(PFS) )和中枢神经系统(CSS)少转移性疾病患者的OS。对于获得性耐药EGFR-TKI的非小细胞肺癌,应考虑将MWA作为治疗中枢神经系统少细胞转移性疾病的局部疗法。

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