Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Collaborative Innovation Center for Cancer Medicine, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China.
Department of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Int J Cancer. 2025 Jan 1;156(1):174-185. doi: 10.1002/ijc.35139. Epub 2024 Aug 26.
Hepatic metachronous oligometastatic nasopharyngeal carcinoma (hmoNPC) exhibits distinct clinical characteristics compared to other types of metastatic NPC. We investigated the optimal therapy for hmoNPC. 160 patients with hmoNPC treated in Sun Yat-sen University Cancer Center between 2010 and 2021 were retrospectively recruited. A total of 56 patients were classified into the local therapy (LT) cohort, 23 into the systemic therapy (ST) cohort and 81 into the combination therapy (LT + ST) cohort. The median PFS was 7.9 months (95% confidence interval [CI]: 4.1-11.9 months) in the LT cohort, 15.5 months (95% CI: 10.5-32.3 months) in the ST cohort, and 31.3 months (95% CI: 20.3 to NA months) in the LT + ST cohort. The median OS was 41.1 months (95% CI: 30.0-54.0 months) in the LT cohort, 50.4 months (95% CI: 41.5 to NA months) in the ST cohort and not reached (NR) (95% CI: 77.3 to NA months) in the LT + ST cohort. Cox analysis was used to construct nomograms to predict patient outcomes. Among patients with no evidence of disease status after LT, the prognosis was significantly better in the LT + ST cohort than LT cohort (median PFS: NR [95% CI: 29.0 to NA months] vs. 20.0 months [95% CI: 10.4 to NA months]). More survival benefits were achieved with platinum-based chemotherapy than oral monotherapy (median PFS: NR [95% CI: 21.7 to NA months] vs. 17.2 months [95% CI: 10.2 to NA months]). Fewer postoperative early progression events were observed in neoadjuvant chemotherapy cohort than in adjuvant chemotherapy cohort (2.78% vs. 18.81%, P = .013). In conclusion, combining neoadjuvant platinum-based chemotherapy and local therapy was the best strategy for patients with hmoNPC.
肝转移同期寡转移鼻咽癌(hmoNPC)与其他转移性 NPC 相比具有明显的临床特征。我们研究了 hmoNPC 的最佳治疗方法。
回顾性招募了 2010 年至 2021 年在中山大学肿瘤防治中心治疗的 160 例 hmoNPC 患者。共有 56 例患者归入局部治疗(LT)组,23 例归入系统治疗(ST)组,81 例归入联合治疗(LT+ST)组。LT 组的中位无进展生存期(PFS)为 7.9 个月(95%CI:4.1-11.9 个月),ST 组为 15.5 个月(95%CI:10.5-32.3 个月),LT+ST 组为 31.3 个月(95%CI:20.3-NR 个月)。LT 组的中位总生存期(OS)为 41.1 个月(95%CI:30.0-54.0 个月),ST 组为 50.4 个月(95%CI:41.5-NR 个月),LT+ST 组未达到(NR)(95%CI:77.3-NR 个月)。Cox 分析用于构建预测患者结局的列线图。在 LT 后无疾病状态的患者中,LT+ST 组的预后明显优于 LT 组(中位 PFS:NR[95%CI:29.0-NR 个月]vs.20.0 个月[95%CI:10.4-NR 个月])。与口服单药治疗相比,铂类化疗具有更好的生存获益(中位 PFS:NR[95%CI:21.7-NR 个月]vs.17.2 个月[95%CI:10.2-NR 个月])。新辅助化疗组术后早期进展事件少于辅助化疗组(2.78%vs.18.81%,P=0.013)。
总之,新辅助铂类化疗联合局部治疗是 hmoNPC 患者的最佳治疗策略。