Department 8-Clinical Medicine, Carol Davila University of Medicine and Pharmacy, 8 Sanitary Heroes Boulevard, 050474 Bucharest, Romania.
Department of Medical Oncology, Elias Emergency University Hospital, 17 Bd. Marasti, 011461 Bucharest, Romania.
Medicina (Kaunas). 2024 Aug 9;60(8):1290. doi: 10.3390/medicina60081290.
Ovarian cancer, including tubal and peritoneal cancer, is the third most common gynecological cancer and the leading cause of death from gynecological malignancies in developed countries. This study explores the prognostic value of the neutrophil-to-lymphocyte ratio (NLR) in determining the optimal duration of neoadjuvant chemotherapy (NACT) for advanced ovarian cancer. It also investigates the correlation between NLR dynamics and the KELIM score, a chemosensitivity marker, to enhance individualized therapeutic strategies. A total of 79 patients underwent NACT followed by interval debulking surgery (IDS) or palliative care. The data collected included demographic information, tumor characteristics, treatment modalities, and laboratory parameters. The baseline NLR (NLR-T0) and post-therapeutic NLR (NLR-T1) were calculated, and their variation (NLR∆) was analyzed. The KELIM score was determined using CA-125 values. Patients with a high baseline NLR (≥2.5) had significantly worse progression-free survival (PFS) and overall survival (OS) compared to those with a low NLR (<2.5). A negative NLR∆ was associated with poorer PFS and OS. The KELIM score indicated a more effective treatment response, with higher scores correlating with better outcomes. The majority of patients achieved R0 resection, and those with favorable KELIM scores showed improved survival rates. The NLR is a valuable prognostic marker for assessing treatment response and guiding NACT duration in advanced ovarian cancer.
卵巢癌包括输卵管癌和腹膜癌,是第三大常见妇科癌症,也是发达国家妇科恶性肿瘤死亡的主要原因。本研究探讨中性粒细胞与淋巴细胞比值(NLR)在确定晚期卵巢癌新辅助化疗(NACT)最佳持续时间中的预后价值。它还研究了 NLR 动态与化疗敏感性标志物 KELIM 评分之间的相关性,以增强个体化治疗策略。
共有 79 名患者接受了 NACT 治疗,随后进行了间隔减瘤手术(IDS)或姑息治疗。收集的数据包括人口统计学信息、肿瘤特征、治疗方式和实验室参数。计算了基线 NLR(NLR-T0)和治疗后 NLR(NLR-T1),并分析了它们的变化(NLR∆)。使用 CA-125 值确定 KELIM 评分。
基线 NLR 较高(≥2.5)的患者与 NLR 较低(<2.5)的患者相比,无进展生存期(PFS)和总生存期(OS)明显更差。NLR∆为负与较差的 PFS 和 OS 相关。KELIM 评分表明治疗反应更有效,得分越高,结果越好。大多数患者达到了 R0 切除,KELIM 评分良好的患者生存率提高。
NLR 是评估治疗反应和指导晚期卵巢癌 NACT 持续时间的有价值的预后标志物。