RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
英文原题:Short- and long-term efficacy of olaparib combined with chemotherapy in advanced triple-negative breast cancer.
Short- and long-term efficacy of olaparib combined with chemotherapy in advanced triple-negative breast cancer.
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奥拉帕利联合化疗增强了晚期 TNBC 的短期和长期疗效,改善了免疫功能,并延长了生存期,且未增加治疗相关毒性,支持其临床应用。
评估奥拉帕利联合化疗作为辅助治疗对晚期三阴性乳腺癌(TNBC)患者的短期和长期疗效。
这项回顾性队列研究纳入274例晚期TNBC患者,分为观察组(olaparib + 化疗,n = 116)和对照组(单纯化疗,n = 158)。主要结局指标包括客观缓解率(ORR)、疾病控制率(DCR)、免疫功能指标(CD3+、CD4+/CD8+比值、自然杀伤T细胞)、细胞因子水平(干扰素-γ、白细胞介素-2、白细胞介素-6)、肿瘤标志物[癌胚抗原、糖类抗原153、人附睾蛋白4]、Karnofsky功能状态评分(KPS)、无进展生存期(PFS)、总生存期(OS)及不良事件发生率。
观察组ORR和DCR均显著高于对照组(均P < 0.05)。观察组免疫功能和细胞因子水平显著改善(均P < 0.05)。相比之下,对照组IL-6水平显著升高(P < 0.05)。观察组肿瘤标志物水平较低(均P < 0.001)。观察组治疗后1、3、6个月KPS评分显著较高(均P < 0.05)。观察组PFS和OS均延长(均P < 0.05)。
To evaluate the short- and long-term efficacy of olaparib combined with chemotherapy as adjuvant therapy in patients with advanced triple-negative breast cancer (TNBC).
This retrospective cohort study included 274 patients with advanced TNBC, divided into an observation group (olaparib + chemotherapy, n = 116) and a control group (chemotherapy alone, n = 158). Primary outcome measures included Objective Response Rate (ORR), Disease Control Rate (DCR), immune function indicators (CD3+, CD4+/CD8+ ratio, Natural Killer T cells), cytokine levels (Interferon-gamma, Interleukin-2, Interleukin-6), tumor markers [Carcinoembryonic Antigen, Carbohydrate Antigen 153, Human Epididymis Protein 4], Karnofsky Performance Status (KPS), Progression-Free Survival (PFS), Overall Survival (OS), and adverse event incidence.
The observation group showed significantly higher ORR and DCR (both P < 0.05) than the control group. Immune function and cytokine levels improved significantly in the observation group (both P < 0.05). In contrast, IL-6 levels increased significantly in the control group (P < 0.05). Tumor marker levels were lower in the observation group (all P < 0.001). KPS scores were significantly higher in the observation group at 1, 3, and 6 months post-treatment (all P < 0.05). The observation group exhibited prolonged PFS and OS (both P < 0.05).
Olaparib combined with chemotherapy enhances short- and long-term efficacy, improves immune function, and prolongs survival in advanced TNBC without increasing treatment-related toxicity, supporting its clinical utility.
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