Department of Respiratory Medicine, Second Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, China.
Department of Respiratory and Critical Care Medicine, The Fourth Affiliated Hospital, International Institutes of Medicine, Zhejiang University School of Medicine, Yiwu, China.
Clin Respir J. 2024 May;18(5):e13761. doi: 10.1111/crj.13761.
In order to improve survival outcomes in resectable non-small cell lung cancer (NSCLC), strategies for neoadjuvant therapy need to be revisited. We evaluated and compared the efficacy of different neoadjuvant therapeutic modalities in a real-world setting.
A total of 258 patients with clinical stage IIA to IIIB NSCLC was included. All the patients underwent surgical resection after one to four cycles of neoadjuvant treatment consisting of chemotherapy (83), immunotherapy (23), and immunotherapy plus chemotherapy (152).
The radiologic response rate in the combined immunochemotherapy group was 67.8%, higher than that of 48.2% in the chemotherapy group and 4.3% in the immunotherapy group (p < 0.001). An improved major pathological response (MPR) was also achieved in the combined therapy group compared with the chemotherapy group and the immunotherapy group (53.9% vs. 10.8% vs. 8.7%, p < 0.001). Patients in the combined therapy group had a significant trend toward longer disease-free survival than those in the chemotherapy alone group (3-year disease-free survival [DFS] of 68.79% vs. 50.81%; hazard ratio [HR] for progression or death, 0.477; p = 0.003). Multivariate Cox analysis identified radical surgery (HR, 0.328; p = 0.033), ypN0-1 stage (HR, 0.591; p = 0.038) and MPR result (HR, 0.362; p = 0.007) to be independent prognostic factors for DFS.
Neoadjuvant treatment with a combination of immunotherapy plus chemotherapy appears to achieve higher radiological and pathological responses than monotherapy for IIA-IIIB NSCLC. Log-rank analysis showed that a better outcome could be expected in patients with the addition of immunotherapy to neoadjuvant chemotherapy if compared with patients with chemotherapy alone in terms of DFS.
为了提高可切除非小细胞肺癌(NSCLC)的生存结果,需要重新审视新辅助治疗策略。我们在真实环境中评估和比较了不同新辅助治疗方式的疗效。
共纳入 258 例临床 IIA 期至 IIIB 期 NSCLC 患者。所有患者在接受一至四个周期的新辅助治疗后接受手术切除,新辅助治疗方案包括化疗(83 例)、免疫治疗(23 例)和免疫联合化疗(152 例)。
联合免疫化疗组的影像学缓解率为 67.8%,高于化疗组的 48.2%和免疫治疗组的 4.3%(p<0.001)。与化疗组和免疫治疗组相比,联合治疗组也实现了更好的主要病理缓解(MPR)(53.9%比 10.8%比 8.7%,p<0.001)。联合治疗组患者的无病生存期明显长于单纯化疗组(3 年无病生存率[DFS]为 68.79%比 50.81%;进展或死亡的风险比[HR]为 0.477;p=0.003)。多因素 Cox 分析确定根治性手术(HR,0.328;p=0.033)、ypN0-1 期(HR,0.591;p=0.038)和 MPR 结果(HR,0.362;p=0.007)是 DFS 的独立预后因素。
与单独化疗相比,免疫治疗联合化疗新辅助治疗似乎能为 IIA-IIIB NSCLC 患者带来更高的影像学和病理学缓解率。对数秩分析显示,与单独化疗相比,如果新辅助化疗中加入免疫治疗,DFS 方面可能会有更好的结果。