Medical Oncology Unit, Depart. of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
Medical Oncology Unit, Ospedale Buccheri La Ferla, Palermo, Italy.
In Vivo. 2020 Jul-Aug;34(4):2009-2014. doi: 10.21873/invivo.11999.
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.
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.
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.
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.
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。
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。
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。
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。