Wang Zhen, Wei Lingyun, Li Jing, Zhou Han, Li Si, Chen Dongsheng, Yu Yangyang, Zhao Lele, Zhu Xixu, Song Yong
Jinling Hospital, Southern Medical University, Guangzhou, China.
Department of Radiation Oncology, Jinling Hospital, Nanjing, China.
Transl Lung Cancer Res. 2021 Dec;10(12):4368-4379. doi: 10.21037/tlcr-21-682.
Immunotherapy has brought substantial benefit for patients with advanced non-small cell lung cancer (NSCLC); however, resistance may occur, of which oligoprogression is most common. There are no standard strategies to overcome acquired resistance, thus exploring potential effective approaches is critical. Our study evaluated the clinical outcome of combing stereotactic body radiotherapy (SBRT) with checkpoint inhibitors (CPIs) in oligoprogressive NSCLC.
We retrospectively reviewed patients with advanced NSCLC who received SBRT for oligoprogressive lesions after acquired resistance to CPIs in our hospital between January 2015 and January 2021. Acquired resistance was defined as initial complete/partial response (CR/PR) followed by progression/death. Oligo patterns of acquired resistance were defined as progression in ≤2 sites of disease. We evaluated the local control rate (LR), progression-free survival (PFS-PO), overall survival (OS-PO), and safety of combing SBRT after oligoprogression.
Among 177 patients reviewed, 24 patients were included. Fifteen (62.5%) were diagnosed with adenocarcinoma, and 20 (83.3%) were with stage IV. Before oligoprogression, immunotherapy was used as first-line treatment in 16 (66.7%) patients, and 4 (16.7%) received monotherapy. After combing SBRT with CPIs, the median PFS-PO and OS-PO were 11 months (95% CI: 8-NA) and 34 months (95% CI: 19-NA). The median LC of 34 oligoprogressed lesions was 43 months (95% CI: 7.7-78.3). The 1- and 2-year LC rates were 100% and 81.8%, respectively. Patients with adenocarcinoma, lung immune prognostic index (LIPI) (≥1), and positive PD-L1 tended to achieve favorable survival benefits.
We observed considerable benefit of local control and survival by combing SBRT in patients with oligoprogression after required resistance to CPIs in NSCLC. The adverse events are well managed. Our results suggest that combing SBRT with CPIs could be a potential strategy to overcome acquired resistance.
免疫疗法已为晚期非小细胞肺癌(NSCLC)患者带来了显著益处;然而,可能会出现耐药,其中寡进展最为常见。目前尚无克服获得性耐药的标准策略,因此探索潜在的有效方法至关重要。我们的研究评估了立体定向体部放疗(SBRT)联合检查点抑制剂(CPI)治疗寡进展性NSCLC的临床疗效。
我们回顾性分析了2015年1月至2021年1月在我院接受SBRT治疗的晚期NSCLC患者,这些患者在对CPI获得性耐药后出现寡进展性病变。获得性耐药定义为初始完全/部分缓解(CR/PR)后出现进展/死亡。获得性耐药的寡模式定义为疾病进展部位≤2个。我们评估了寡进展后联合SBRT的局部控制率(LR)、无进展生存期(PFS-PO)、总生存期(OS-PO)和安全性。
在177例接受评估的患者中,纳入了24例。15例(62.5%)诊断为腺癌,20例(83.3%)为IV期。在寡进展前,16例(66.7%)患者将免疫疗法作为一线治疗,4例(16.7%)接受单药治疗。SBRT与CPI联合治疗后,中位PFS-PO和OS-PO分别为11个月(95%CI:8-NA)和34个月(95%CI:19-NA)。34个寡进展性病变的中位局部控制时间为43个月(95%CI:7.7-78.3)。1年和2年局部控制率分别为100%和81.8%。腺癌患者、肺免疫预后指数(LIPI)(≥1)和PD-L1阳性患者倾向于获得良好的生存获益。
我们观察到,在NSCLC患者对CPI获得性耐药后出现寡进展时,联合SBRT在局部控制和生存方面有显著益处。不良事件得到了良好管理。我们的结果表明,SBRT与CPI联合可能是克服获得性耐药的一种潜在策略。