Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Front Immunol. 2022 Jun 20;13:918787. doi: 10.3389/fimmu.2022.918787. eCollection 2022.
Whilst survival benefits of thoracic radiotherapy (TRT) followed by immune checkpoint inhibitor (ICI) have been reported in patients with lung cancer, the potential high risk of treatment-related pneumonitis remains a concern. Asians may be more sensitive to lung toxicity than other races. This retrospective study intended to provide a comprehensive pneumonitis profile of TRT followed by ICI and investigate the risk factors from a Chinese cohort of lung cancer.
From January 2016 to July 2021, 196 patients with lung cancer who received TRT prior to ICI were retrospectively analyzed. Treatment-related pneumonitis, including checkpoint inhibitor pneumonitis (CIP), radiation pneumonitis (RP), and radiation recall pneumonitis (RRP), were recorded and graded through medical records and chest computed tomography. Characteristics predictive of pneumonitis were assessed using logistic regression models, and the receiver operating characteristic analyses were performed to identify optimal cut points for quantitative variables.
With a median follow-up of 18 months, a total of 108 patients (55.1%) developed treatment-related pneumonitis during ICI therapy, with an incidence of 25.5% for grade 2 or higher (G2+) and 4.1% for G3+. The overall rates of CIP, RP and RRP were 8.2% (n=16), 46.9% (n=92) and 7.1% (n=14), respectively. With a total mortality rate of 1.5%, vast majority of the patients recovered from pneumonitis or remained stable. No patients died of RRP. Half of the patients with G2+ RP who withheld ICI therapy restarted ICI safely after resolution of RP. The history of chronic pulmonary diseases (=0.05), mean lung dose (MLD, =0.038), percent volume of lung receiving ≥5 Gy (V5, =0.012) and percent volume of lung receiving ≥20 Gy (V20, =0.030) predicted the occurrence of RRP in univariate analyses. Interval between TRT and ICI less than 3 months was an independent predictor for G2+ treatment-related pneumonitis in a multivariate model (Odds ratio OR=2.787, =0.004).
Treatment-related pneumonitis, especially RRP, is acceptable and manageable in the setting of TRT followed by ICI in this Asian population. Dosimetric parameters MLD, V5 and V20 may improve the predictions of RRP in clinical practice.
虽然已有研究表明,对于肺癌患者,接受胸部放疗(TRT)后再接受免疫检查点抑制剂(ICI)治疗可带来生存获益,但治疗相关肺炎的潜在高风险仍然令人担忧。亚洲人可能比其他种族更容易发生肺毒性。本回顾性研究旨在为接受 TRT 后再接受 ICI 治疗的肺癌患者提供全面的肺炎概况,并从中国肺癌患者队列中探讨相关风险因素。
从 2016 年 1 月至 2021 年 7 月,共对 196 例接受 TRT 治疗后再接受 ICI 治疗的肺癌患者进行回顾性分析。通过病历和胸部 CT 记录并分级治疗相关肺炎,包括检查点抑制剂肺炎(CIP)、放射性肺炎(RP)和放射性肺炎再发(RRP)。使用逻辑回归模型评估预测肺炎的特征,并进行受试者工作特征分析,以确定定量变量的最佳截断值。
中位随访 18 个月期间,共有 108 例(55.1%)患者在接受 ICI 治疗期间发生治疗相关肺炎,其中 2 级或以上(G2+)发生率为 25.5%,3 级发生率为 4.1%。CIP、RP 和 RRP 的总发生率分别为 8.2%(n=16)、46.9%(n=92)和 7.1%(n=14)。总死亡率为 1.5%,大多数患者肺炎缓解或保持稳定,无患者死于 RRP。半数 G2+RP 患者在 RP 缓解后停用 ICI 治疗,重新安全地开始 ICI 治疗。有慢性肺部疾病史(=0.05)、平均肺剂量(MLD,=0.038)、接受≥5 Gy 的肺体积百分比(V5,=0.012)和接受≥20 Gy 的肺体积百分比(V20,=0.030)在单因素分析中预测了 RRP 的发生。TRT 和 ICI 之间的时间间隔小于 3 个月是多因素模型中 G2+治疗相关肺炎的独立预测因素(优势比 OR=2.787,=0.004)。
在该亚洲人群中,TRT 后再接受 ICI 治疗的患者中,治疗相关肺炎,尤其是 RRP,是可接受且可管理的。MLD、V5 和 V20 等剂量学参数可能会提高 RRP 在临床实践中的预测效果。