Université de Paris, Institut du Cancer Paris CARPEM, F-75006 Paris, France; Department of medical oncology, APHP.Centre, Hopital Cochin, Paris, France.
Université de Paris, Institut du Cancer Paris CARPEM, F-75006 Paris, France; Department of gynecological surgery, APHP.Centre, Hopital Cochin, Paris, France; Centre de Recherche des Cordeliers, « Equipe labélisée Ligue Contre le Cancer », Sorbonne Université, Université de Paris, INSERM UMR1138, Paris, France.
Gynecol Oncol. 2022 Aug;166(2):269-276. doi: 10.1016/j.ygyno.2022.05.016. Epub 2022 May 26.
Adjuvant therapeutic decisions in older endometrial carcinoma (EC) patients are challenged by a balance between more frequent aggressive EC and comorbidities. We assessed whether EC and comorbidities are competing or cumulative risks in older EC patients.
All consecutive patients treated for FIGO stage I-IV EC in two University Hospitals in Paris between 2010 and 2017 were retrospectively included. Patients were categorized as: <70 years (y), >70y without comorbidity (fit), and > 70y with a Charlson comorbidity index>3 (comorbid). Association between high-risk EC (2021-ESGO-ETRO-ESP) or comorbidity, and disease-specific-survival (DSS), was evaluated using Cox model (estimation of cause-specific hazard ratio (CSHR), and Fine-Gray model (subdistribution HR) to account for competing events (death unrelated with EC).
Overall, 253 patients were included (median age = 67y, IQR[59-77], median follow-up = 61.5 months, [44.4-76.8]). Among them, 109 (43%) were categorized at high-risk (proportion independent of age), including 67 (26%) who had TP53-mutated tumors. Comorbidity and high-risk group were both associated with all-cause mortality (HR = 4.09, 95%CI[2.29; 7.32] and HR = 3.21, 95%CI [1.69; 6.09], respectively). By multivariate analysis, patients with high-risk EC exhibited poorer DSS, regardless of age/comorbidity (Adjusted-CSHR = 6.62, 95%CI[2.53;17.3]; adjusted-SHR = 6.62 95%CI[2.50;17.5]). Patients>70y-comorbid with high-risk EC had 5-years cumulative incidences of EC-related and EC-unrelated death of 29% and 19%, respectively. In patients <70y, 5-years cumulative incidence of EC-related and EC-unrelated death were 25% and < 1% (one event), respectively.
High-risk EC patients are exposed to poorer DSS regardless of age/comorbidities, comorbidities and cancer being two cumulative rather than competing risks. Our results suggest that age/comorbidity alone should not lead to underestimate EC-specific survival.
在老年子宫内膜癌(EC)患者中,辅助治疗决策面临着更频繁的侵袭性 EC 和合并症之间的平衡。我们评估了 EC 和合并症是否是老年 EC 患者的竞争或累积风险。
回顾性纳入 2010 年至 2017 年期间在巴黎两家大学医院接受 FIGO 分期 I-IV 期 EC 治疗的所有连续患者。患者分为:<70 岁(y),>70y 无合并症(fit),>70y 合并 Charlson 合并症指数>3(合并症)。使用 Cox 模型(估计特定原因的危险比(CSHR)和 Fine-Gray 模型(亚分布 HR)来评估高危 EC(2021-ESGO-ETRO-ESP)或合并症与疾病特异性生存(DSS)之间的关联,以考虑竞争事件(与 EC 无关的死亡)。
总体而言,纳入了 253 名患者(中位年龄=67y,IQR[59-77],中位随访=61.5 个月,[44.4-76.8])。其中,109 名(43%)患者被归类为高危(与年龄无关的比例),包括 67 名(26%)肿瘤存在 TP53 突变。合并症和高危组均与全因死亡率相关(HR=4.09,95%CI[2.29;7.32]和 HR=3.21,95%CI [1.69;6.09])。通过多变量分析,无论年龄/合并症如何,患有高危 EC 的患者 DSS 较差(调整后的 CSHR=6.62,95%CI[2.53;17.3];调整后的 SHR=6.62 95%CI[2.50;17.5])。>70y 岁合并高危 EC 的患者 5 年 EC 相关和 EC 无关死亡的累积发生率分别为 29%和 19%。在<70y 岁的患者中,5 年 EC 相关和 EC 无关死亡的累积发生率分别为 25%和<1%(1 例)。
无论年龄/合并症如何,高危 EC 患者的 DSS 均较差,合并症和癌症是两个累积而非竞争的风险。我们的结果表明,年龄/合并症本身不应导致低估 EC 特异性生存率。