Department of Oral and Maxillofacial-Head and Neck Oncology, Beijing Stomatological Hospital, Capital Medical University, Beijing, 100050, China.
Department of Oral and Maxillofacial-Head and Neck Oncology, Beijing Stomatological Hospital, Capital Medical University, Beijing, 100050, China.
J Craniomaxillofac Surg. 2024 Feb;52(2):260-268. doi: 10.1016/j.jcms.2023.12.011. Epub 2024 Jan 3.
This study aimed to reveal the underlying mechanisms linking advanced oral squamous cell carcinoma (OSCC) with its comorbidities. Data extracted from the POROMS database included 448 advanced OSCC patients in stage III or IV (AJCC 8th) with primary tumors between August 2015 and August 2021. Time to diagnosis delay increased from 4.5, 5.3-6.5 months when the Adult Comorbidity Evaluation-27 (ACE-27) worsened from none, mild (RR: 1.155, 1.043-1.279; P = 0.006) to moderate-severe (RR: 1.431, 1.251-1.636; P < 0.001). With the number of comorbidities increased from 0, 1-2 (RR: 1.188, 1.078-1.310; P = 0.001) to 3 (RR: 1.563, 1.296-1.885; P < 0.001), the time to diagnosis delay increased from 4.5, 5.4-7.1 months. As the level and number of comorbidities increased, the likelihood of treatment completion gradually declined, especially in those older than 65 years (P = 0.003). The presence of comorbidity was an independent prognostic factor for disease-free survival (HR: 1.431, 1.022-2.005; P = 0.037). Comorbidities may lead to poorer prognosis by directly causing delays in diagnosis, limiting treatment options, and increasing the risk of death in advanced OSCC patients.
本研究旨在揭示晚期口腔鳞状细胞癌(OSCC)与其合并症之间的潜在机制。POROMS 数据库中提取的数据包括 448 名处于 III 期或 IV 期(第 8 版 AJCC)的晚期 OSCC 患者,其原发肿瘤在 2015 年 8 月至 2021 年 8 月之间。当成人合并症评估-27(ACE-27)从无、轻度(RR:1.155,1.043-1.279;P=0.006)恶化至中度-重度(RR:1.431,1.251-1.636;P<0.001)时,诊断延迟时间从 4.5 个月增加至 5.3-6.5 个月。随着合并症数量从 0、1-2(RR:1.188,1.078-1.310;P=0.001)增加至 3(RR:1.563,1.296-1.885;P<0.001),诊断延迟时间从 4.5 个月增加至 5.4-7.1 个月。随着合并症水平和数量的增加,治疗完成的可能性逐渐降低,尤其是 65 岁以上的患者(P=0.003)。合并症的存在是无病生存的独立预后因素(HR:1.431,1.022-2.005;P=0.037)。合并症可能通过直接导致诊断延迟、限制治疗选择以及增加晚期 OSCC 患者死亡风险,从而导致较差的预后。