Belgian Health Care Knowledge Centre (KCE), Boulevard du Jardin Botanique 55, B-1000 Brussels, Belgium.
Belgian Cancer Registry, Rue Royale 215, B-1210 Brussels, Belgium.
Oral Oncol. 2020 Mar;102:104561. doi: 10.1016/j.oraloncology.2019.104561. Epub 2020 Jan 7.
This study aims to investigate the relationship between comorbidities and therapeutic delay, post-treatment mortality, overall and relative survival in patients diagnosed with squamous cell carcinoma of the head and neck (HNSCC).
9245 patients with a single HNSCC diagnosed between 2009 and 2014 were identified in the Belgian Cancer Registry. The Charlson Comorbidity Index (CCI) was calculated for 8812 patients (95.3%), distinguishing patients having none (0), mild (1-2), moderate (3-4) or severe comorbidity (>4). The relationship between CCI and therapeutic delay was evaluated using the Spearman correlation. Post-treatment mortality was modelled with logistic regression, using death within 30 days as the event. The association between comorbidity and survival was assessed using Cox proportional hazard models.
Among 8812 patients with a known CCI, 39.2% had at least one comorbidity. Therapeutic delay increased from 31 to 36 days when the CCI worsened from 0 to 4 (rho = 0.087). After case-mix adjustment, higher baseline comorbidity was associated with increased post-surgery mortality (mild, OR 3.52 [95% CI 1.91-6.49]; severe, OR 18.71 [95% CI 6.85-51.12]) and post-radiotherapy mortality (mild, OR 2.23 [95% CI 1.56-3.19]; severe, OR 9.33 [95% CI 4.83-18.01]) and with reduced overall survival (mild, HR 1.39, [95% CI 1.31-1.48]; severe, HR 2.41 [95% CI 2.00-2.90]). That was also the case for relative survival in unadjusted analyses (mild, EHR 1.77 [95% CI 1.64-1.92]; severe, EHR = 4.15 [95% CI 3.43-5.02]).
Comorbidity is significantly related to therapeutic delay, post-treatment mortality, 5-year overall and relative survival in HNSCC patients. Therapeutic decision support tools should optimally integrate comorbidity.
本研究旨在探讨合并症与治疗延迟、治疗后死亡率、头颈部鳞状细胞癌(HNSCC)患者的总生存率和相对生存率之间的关系。
在比利时癌症登记处,共确定了 9245 名 2009 年至 2014 年间确诊为单一 HNSCC 的患者。对 8812 名患者(95.3%)计算了 Charlson 合并症指数(CCI),并将患者分为无合并症(0)、轻度(1-2)、中度(3-4)或重度合并症(>4)。使用 Spearman 相关系数评估 CCI 与治疗延迟之间的关系。使用死亡发生在 30 天内作为事件,使用逻辑回归模型对治疗后死亡率进行建模。使用 Cox 比例风险模型评估合并症与生存之间的关联。
在 8812 名已知 CCI 的患者中,39.2%至少有一种合并症。当 CCI 从 0 增加到 4 时,治疗延迟从 31 天增加到 36 天(rho=0.087)。在病例组合调整后,基线合并症较高与术后死亡率增加相关(轻度,OR 3.52[95%CI 1.91-6.49];重度,OR 18.71[95%CI 6.85-51.12])和放疗后死亡率增加(轻度,OR 2.23[95%CI 1.56-3.19];重度,OR 9.33[95%CI 4.83-18.01])以及总生存率降低(轻度,HR 1.39[95%CI 1.31-1.48];重度,HR 2.41[95%CI 2.00-2.90])。在未调整分析中,相对生存率也存在这种情况(轻度,EHR 1.77[95%CI 1.64-1.92];重度,EHR=4.15[95%CI 3.43-5.02])。
合并症与 HNSCC 患者的治疗延迟、治疗后死亡率、5 年总生存率和相对生存率显著相关。治疗决策支持工具应最佳地整合合并症。