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寡进展期非小细胞肺癌患者接受表皮生长因子受体酪氨酸激酶抑制剂治疗后行大剂量放疗:真实世界数据。

High-dose Radiotherapy for Oligo-progressive NSCLC Receiving EGFR Tyrosine Kinase Inhibitors: Real World Data.

机构信息

Medical Oncology Unit, Depart. of Human Pathology "G. Barresi", University of Messina, Messina, Italy.

Medical Oncology Unit, Ospedale Buccheri La Ferla, Palermo, Italy.

出版信息

In Vivo. 2020 Jul-Aug;34(4):2009-2014. doi: 10.21873/invivo.11999.

Abstract

BACKGROUND/AIM: Local ablative treatments for oligo-progressive, EGFR mutated non-small cell lung cancer (mut-NCSLC) may improve long-term disease control and survival. We analyzed the efficacy of hypo-fractionated, high-dose radiation therapy (HDRT), in association with prolonged EGFR tyrosine kinase inhibitors (TKI) in oligo-progressive, EGFR mutant-NSCLC.

PATIENTS AND METHODS

Progression-free survival-1 (PFS-1, date from initiation of TKI therapy until oligo-progression or death), and progression-free survival-2 (PFS-2, date of focal progression until further progression or death) were evaluated.

RESULTS

Thirty-six patients were analyzed. The median PFS 1 was 12.5 months. HDHRT consisted of intensity-modulated RT and stereotactic RT in 23 (64%) and 13 (36%) patients respectively. The median PFS 2 was 6.3 months. Overall survival was 38.7 months.

CONCLUSION

Hypo-fractionated HDRT plus TKI therapy, is associated with a significant prolongation of disease control (overall PFS: 18.8 months), with manageable side effects. These real-world data support the use of local ablative approaches in oligo-progressive EGFR mut-NSCLC.

摘要

背景/目的:局部消融治疗寡进展性、表皮生长因子受体(EGFR)突变型非小细胞肺癌(mut-NCSLC)可能改善长期疾病控制和生存。我们分析了低分割、高剂量放射治疗(HDRT)联合延长 EGFR 酪氨酸激酶抑制剂(TKI)治疗寡进展性、EGFR 突变型 NSCLC 的疗效。

患者和方法

无进展生存期 1(PFS-1,从开始 TKI 治疗到寡进展或死亡的时间)和无进展生存期 2(PFS-2,从局部进展到进一步进展或死亡的时间)进行了评估。

结果

分析了 36 例患者。中位 PFS1 为 12.5 个月。23 例(64%)和 13 例(36%)患者分别接受了调强放疗和立体定向放疗。中位 PFS2 为 6.3 个月。总生存期为 38.7 个月。

结论

低分割 HDRT 联合 TKI 治疗与疾病控制的显著延长相关(总 PFS:18.8 个月),且副作用可管理。这些真实世界的数据支持在寡进展性 EGFR mut-NCSLC 中使用局部消融方法。

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