Yan Chang, Zhao Rong, Chen Kai-Hua, Chen Biao-You, Zhang Chao-Jun, Chen Xi, Meng Wan-Wan, Lai Lin, Qu Song, Zhu Xiao-Dong
Department of Radiation Oncology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530021, People's Republic of China.
Department of Oncology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, 530199, People's Republic of China.
J Cancer. 2023 Oct 9;14(17):3368-3377. doi: 10.7150/jca.87901. eCollection 2023.
To explore the prognostic value of clinical and serological risk factors for progression-free survival (PFS) in stage II and T3N0 nasopharyngeal carcinoma (NPC) and construct a nomogram based on these factors. Additionally, to investigate the long-term survival and short-term toxic reactions of patients in different risk stratification under different treatment modalities. The patients were randomly divided into training and validation cohorts in a 7:3 ratio. Independent prognostic factors were identified using Cox regression analysis, and a nomogram was constructed by combining these predictive factors with the TNM staging system. The nomogram was then validated in the validation cohort, and patients were classified into different risk groups based on the nomogram. The PFS, overall survival (OS), and acute toxicities were compared among different treatment modalities after balancing baseline characteristics. Multivariate Cox regression analysis indicated that pathological type, alkaline phosphatase (ALP) and lactate dehydrogenase (LDH) were independent prognostic factors(p<0.05) in this study. The nomogram showed good prognostic accuracy in both the training and validation cohorts (C-index of 0.73 and 0.70, respectively). In the different risk subgroups, there were no statistically significant differences in PFS and OS between radiotherapy and chemoradiotherapy groups(p>0.05). The treatment modality of combined chemotherapy was associated with more acute toxic reactions. We established and validated a nomogram for predicting PFS in patients with stage II/T3N0 NPC. Intensity-modulated radiation therapy (IMRT) combined with chemotherapy did not provide additional survival benefits for these patients and was associated with more chemotherapy-related side effects.
探讨临床和血清学危险因素对Ⅱ期和T3N0鼻咽癌(NPC)无进展生存期(PFS)的预后价值,并基于这些因素构建列线图。此外,研究不同治疗模式下不同风险分层患者的长期生存情况和短期毒性反应。患者按7:3的比例随机分为训练队列和验证队列。采用Cox回归分析确定独立预后因素,并将这些预测因素与TNM分期系统相结合构建列线图。然后在验证队列中对列线图进行验证,并根据列线图将患者分为不同风险组。在平衡基线特征后,比较不同治疗模式下的PFS、总生存期(OS)和急性毒性反应。多因素Cox回归分析表明,病理类型、碱性磷酸酶(ALP)和乳酸脱氢酶(LDH)是本研究中的独立预后因素(p<0.05)。列线图在训练队列和验证队列中均显示出良好的预后准确性(C指数分别为0.73和0.70)。在不同风险亚组中,放疗组和放化疗组之间的PFS和OS无统计学显著差异(p>0.05)。联合化疗的治疗模式与更多急性毒性反应相关。我们建立并验证了一个用于预测Ⅱ期/T3N0 NPC患者PFS的列线图。调强放射治疗(IMRT)联合化疗并未为这些患者带来额外的生存获益,且与更多化疗相关副作用相关。