Medical Oncology Department, Kisla Campus, Adana Baskent University, Adana 01120, Turkey.
Adana State Hospital, Adana 01150, Turkey.
Medicina (Kaunas). 2023 Sep 8;59(9):1625. doi: 10.3390/medicina59091625.
: This study evaluated the relationship between microsatellite status (MSI) and pan-immune-inflammation score (PIV) in tumor response to neoadjuvant chemotherapy (NAC) in patients with clinical stage III gastric cancer (cStage III GC). : Microsatellite instability (MSI) status was evaluated based on pathology preparations. Pan-immune-inflammation score (PIV) was obtained from pre-treatment blood tests. The relationship of both parameters with pathological complete response (pCR) was evaluated. : A total of 104 patients were included in this study. All the patients were stage III GC patients receiving perioperative treatment. There were 13 patients in total who achieved a pCR response. While CNS was detected in 11 of the patients who achieved a pCR, the MSI status of the other two patients was unknown. No pCR was observed in any patient with MSI-H. According to the cut-off value for PIV, 25 (24%) patients were in the PIV-low (≤53.9) group, while 79 (76%) were in the PIV-high (>53.9) group. Based on univariate analysis, a higher PIV was associated with worse outcomes for pathological response, disease recurrence, and survival ( < 0.05). : In patients with clinically stage III GC, the presence of MSI-H may predict no benefit from perioperative treatment. Conversely, a pre-treatment PIV score using specific cut-off values may provide a positive prediction of pathological response and survival.
本研究评估了微卫星状态(MSI)和泛免疫炎症评分(PIV)与临床 III 期胃癌(cStage III GC)患者新辅助化疗(NAC)肿瘤反应之间的关系。微卫星不稳定性(MSI)状态基于病理标本进行评估。泛免疫炎症评分(PIV)从治疗前的血液检查中获得。评估了这两个参数与病理完全缓解(pCR)的关系。
共有 104 名患者纳入本研究。所有患者均为接受围手术期治疗的 III 期 GC 患者。共有 13 例患者达到 pCR 反应。在达到 pCR 的 11 例患者中检测到 CNS,但另外 2 例患者的 MSI 状态未知。任何 MSI-H 患者均未观察到 pCR。根据 PIV 的截止值,25 例(24%)患者为 PIV 低(≤53.9)组,79 例(76%)患者为 PIV 高(>53.9)组。基于单因素分析,较高的 PIV 与病理反应、疾病复发和生存不良相关(<0.05)。
在临床 III 期 GC 患者中,MSI-H 的存在可能预示着围手术期治疗无益。相反,使用特定截止值的治疗前 PIV 评分可能对病理反应和生存提供积极预测。