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 Radiation Oncology, National Cancer Center/ Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Thorac Cancer. 2021 Mar;12(6):814-823. doi: 10.1111/1759-7714.13816. Epub 2021 Jan 27.
Concurrent epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKI) with radiotherapy in patients with EGFR-mutant unresectable stage III non-small cell lung cancer (NSCLC) might improve survival. However, both treatments carry a potential risk of pneumonitis.
Between May 2012 and December 2017, patients with unresectable stage III NSCLC treated with concurrent radiotherapy and EGFR-TKI were enrolled in this retrospective study. The baseline characteristics were evaluated to determine correlations with toxicity development.
Among 45 eligible patients, 20 (44.4%) had an EGFR mutation and 44 (97.8%) received 50-66 Gy of radiotherapy. The median follow-up was 62.7 months. The median progression free survival (PFS) and overall survival (OS) for patients with EGFR-mutations were 27.9 (95% CI: 18.7-37.2) and 49.7 (95% CI: 27.7-71.8) months, and 13.8 (95% CI: 8.8-18.9) and 31.1 (95% CI: 9.8-52.4) months for EGFR wild-type/unknown patients. A total of 17 patients (37.7%) developed radiation pneumonitis/pneumonitis (14 grade 2, 3 grade 3). In 16 patients, pneumonitis occurred within the radiation field and one patient had bilateral pneumonitis. The median time from the initial radiotherapy to pneumonitis was 74 days. Logistic regression analysis revealed a trend between the time of EGFR-TKI and the development of G2+ pneumonitis. For late toxicity, only two patients had G2+ fibrosis. The daily dyspnea symptoms of patients with G2+ pneumonitis recovered significantly after the phase of pneumonitis (P = 0.007).
Combined EGFR-TKI and radiotherapy showed favorable survival in EGFR-mutant patients with inoperable stage III NSCLC, with a 6.7% incidence of grade 3 radiation pneumonitis/pneumonitis, despite a higher incidence of mild-to-moderate radiation pneumonitis.
SIGNIFICANT FINDINGS OF THE STUDY: We evaluated the outcomes and radiation pneumonitis after EGFR-TKI during interval radiotherapy. EGFR-TKI plus radiotherapy increased survival in patients with EGFR-mutant inoperable stage III NSCLC. The mild-to-moderate radiation pneumonitis incidence increased but no grade 4--5 adverse events occurred.
The combination of EGFR-TKI and radiotherapy might carry a risk of pneumonitis; however, there are limited data concerning dose constraints. Our results showed a slightly higher incidence of mild or moderate radiation pneumonitis by strict dose limitation.
表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)与放疗联合应用于表皮生长因子受体(EGFR)突变的不可切除 III 期非小细胞肺癌(NSCLC)患者可能会改善生存。然而,这两种治疗方法都有发生肺炎的潜在风险。
2012 年 5 月至 2017 年 12 月,本回顾性研究纳入了接受不可切除 III 期 NSCLC 同步放疗和 EGFR-TKI 治疗的患者。评估基线特征以确定与毒性发展的相关性。
45 例符合条件的患者中,20 例(44.4%)存在 EGFR 突变,44 例(97.8%)接受 50-66 Gy 的放疗。中位随访时间为 62.7 个月。EGFR 突变患者的无进展生存期(PFS)和总生存期(OS)分别为 27.9(95%CI:18.7-37.2)和 49.7(95%CI:27.7-71.8)个月,EGFR 野生型/未知患者的 PFS 和 OS 分别为 13.8(95%CI:8.8-18.9)和 31.1(95%CI:9.8-52.4)个月。17 例(37.7%)发生放射性肺炎/肺炎(14 例 2 级,3 例 3 级)。16 例患者在放疗野内发生肺炎,1 例患者发生双侧肺炎。从初始放疗到肺炎的中位时间为 74 天。Logistic 回归分析显示,EGFR-TKI 开始时间与 G2+肺炎的发生呈趋势相关。对于晚期毒性,只有 2 例患者出现 G2+纤维化。G2+肺炎患者的每日呼吸困难症状在肺炎期后显著恢复(P=0.007)。
对于不可切除的 III 期 EGFR 突变 NSCLC 患者,EGFR-TKI 联合放疗显示出良好的生存结果,3 级放射性肺炎/肺炎的发生率为 6.7%,尽管轻度至中度放射性肺炎的发生率较高。
研究的重要发现:我们评估了 EGFR-TKI 期间间隔放疗期间的疗效和放射性肺炎。EGFR-TKI 联合放疗增加了 EGFR 突变不可切除 III 期 NSCLC 患者的生存。轻度至中度放射性肺炎的发生率增加,但未发生 4-5 级不良事件。
EGFR-TKI 和放疗联合应用可能有发生肺炎的风险,但关于剂量限制的数据有限。我们的结果表明,通过严格的剂量限制,轻度或中度放射性肺炎的发生率略高。