Instituto COI de Pesquisa e Ensino, Rio de Janeiro, Brazil.
Instituto D'Or de Pesquisa e Ensino (IDOR), Rio de Janeiro, Brazil.
JCO Glob Oncol. 2022 Nov;8:e2200061. doi: 10.1200/GO.22.00061.
Stereotactic body radiation therapy (SBRT) is an effective option for patients with both early-stage and oligometastatic non-small-cell lung cancer (NSCLC). However, data from Latin America are limited. Therefore, the aim of this study was to investigate the real-world outcomes of applying SBRT for lung lesions in a Brazilian institution.
This study investigated a consecutive cohort of patients treated with SBRT for lung lesions (primary and metastasis). The study primary outcome was local control rates per lesion. Secondary outcomes included progression-free survival (PFS), overall survival (OS), and toxicity.
Between 2015 and 2019, a total of 216 patients received SBRT and were included in the study. The median follow-up was 24.5 months (5-70), primary NSCLC corresponded to 70% (n = 151) and nonprimary lung lesions to 30% (n = 65), respectively. Stage I NSCLC represented 56% (85 of 151) of the NSCLC cohort. The average number of fractions and total dose prescribed was 5 (3-10)/59 Gy (50-62 Gy). For stage I NSCLC (all lesions treated with a biologically effective dose [10] > 100 Gy), 2-year local control, OS, and PFS were 93.4%, 81.6%, and 80.7%, respectively. For stage IV lesions, if biologically effective dose (10) > 100 Gy or < 100 Gy, 2-year local control was 95.8/86.4% ( = .03), 2-year-OS was 81.6/60.5% ( = .006), and 2-year PFS was 38.9/17.9% ( = .10). Late toxicity was observed in 16.2% (n = 35) of the total cases.
Our results indicate that SBRT is effective (high local control and acceptable toxicity) for treating malignant lung lesions in a real-world scenario in Latin America.
立体定向体部放射治疗(SBRT)是治疗早期和寡转移非小细胞肺癌(NSCLC)患者的有效选择。然而,来自拉丁美洲的数据有限。因此,本研究旨在调查巴西机构应用 SBRT 治疗肺部病变的真实世界结果。
本研究调查了一组连续接受 SBRT 治疗肺部病变(原发性和转移性)的患者。研究的主要结局是每个病变的局部控制率。次要结局包括无进展生存期(PFS)、总生存期(OS)和毒性。
2015 年至 2019 年间,共有 216 例患者接受 SBRT 治疗并纳入研究。中位随访时间为 24.5 个月(5-70),原发性 NSCLC 占 70%(n=151),非原发性肺部病变占 30%(n=65)。Ⅰ期 NSCLC 占 NSCLC 队列的 56%(85/151)。所规定的平均分割次数和总剂量为 5(3-10)/59 Gy(50-62 Gy)。对于Ⅰ期 NSCLC(所有用生物有效剂量[10] > 100 Gy 治疗的病变),2 年局部控制率、OS 和 PFS 分别为 93.4%、81.6%和 80.7%。对于Ⅳ期病变,如果生物有效剂量(10)> 100 Gy 或< 100 Gy,2 年局部控制率为 95.8/86.4%(=.03),2 年 OS 为 81.6/60.5%(=.006),2 年 PFS 为 38.9/17.9%(=.10)。总共有 16.2%(n=35)的病例出现迟发性毒性。
我们的结果表明,SBRT 在拉丁美洲的真实世界环境中治疗恶性肺部病变是有效的(高局部控制率和可接受的毒性)。