The Affiliated Cancer Hospital of Nanjing Medical University, Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.
Jinling Hospital, Jinling School of Clinical Medicine, Nanjing Medical University, Nanjing, Jiangsu, China.
Hum Vaccin Immunother. 2023 Dec 15;19(3):2285902. doi: 10.1080/21645515.2023.2285902. Epub 2023 Nov 27.
This study aimed to investigate the relationship between complete pathological remission (PCR), tertiary lymphoid structure (TLS) maturation and expression and clinical outcomes of patients with resectable non-small cell lung cancer (NSCLC) receiving neoadjuvant chemoimmunotherapy. Totally 80 patients with resectable NSCLC (stage IB-IIIB) receiving neoadjuvant chemoimmunotherapy were analyzed. We used the Kaplan-Meier method to plot survival curves and the log-rank test to compare differences. Among all patients included, 45 patients (56.25%) achieved major pathological response (MPR), including 30 patients (37.50%) with PCR. The proportion of patients diagnosed with stage IB, II, IIIA and IIIB was 1.25%, 10.00%, 52.50% and 36.25%, respectively. We divided patients into PCR group and non-PCR group respectively according to whether they achieved PCR. We found that patients achieving PCR had significantly improved disease-free survival (DFS) (mDFS: NR vs. 20.24 months, = .020). TLS expression was low in 43 cases (53.75%) and high in 37 cases (46.25%). TLS maturation was low in 55 cases (68.75%) and high in 25 cases (31.25%). The DFS of patients with TLS high-maturation (34.07 vs. 22.30 months, = .024) and TLS high-expression (34.07 vs. 22.30 months, = .041) was significantly longer. In most subgroups, the PCR, TLS high-maturation and TLS high-expression group respectively achieved a better clinical outcome relative to the non-PCR, TLS low-maturation and TLS low-expression group. In patients with resectable NSCLC receiving neoadjuvant chemoimmunotherapy, the acquirement of PCR may predict better DFS. In addition, high expression and maturation of TLS may be prognostic factors.
本研究旨在探讨完全病理缓解(PCR)、三级淋巴结构(TLS)成熟度及其表达与接受新辅助化疗免疫治疗的可切除非小细胞肺癌(NSCLC)患者临床结局的关系。共分析了 80 例接受新辅助化疗免疫治疗的可切除 NSCLC(IB-III 期)患者。我们使用 Kaplan-Meier 方法绘制生存曲线,并用对数秩检验比较差异。在所有纳入的患者中,45 例(56.25%)患者获得主要病理缓解(MPR),其中 30 例(37.50%)患者获得 PCR。IB、II、IIIA 和 IIIB 期患者的比例分别为 1.25%、10.00%、52.50%和 36.25%。我们根据是否达到 PCR 将患者分为 PCR 组和非 PCR 组。我们发现,达到 PCR 的患者无病生存期(DFS)显著改善(mDFS:NR 与 20.24 个月, = .020)。TLS 表达低的患者有 43 例(53.75%),高的患者有 37 例(46.25%)。TLS 成熟度低的患者有 55 例(68.75%),高的患者有 25 例(31.25%)。TLS 高成熟(34.07 与 22.30 个月, = .024)和 TLS 高表达(34.07 与 22.30 个月, = .041)的患者 DFS 明显更长。在大多数亚组中,与非 PCR、TLS 低成熟和 TLS 低表达组相比,PCR、TLS 高成熟和 TLS 高表达组分别获得了更好的临床结局。在接受新辅助化疗免疫治疗的可切除 NSCLC 患者中,获得 PCR 可能预示着更好的 DFS。此外,TLS 的高表达和成熟度可能是预后因素。