[建立宫颈腺癌预后提名图并讨论最佳治疗方法:基于 SEER 数据库和中国单中心数据的回顾性研究]。

X Li, Y H Gao, Z Yang, Y Ma, C Liu, G C Liu, D B Wang
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引用次数: 0

摘要

目的基于监测、流行病学和最终结果(SEER)数据库和中国单中心数据,建立并验证宫颈腺癌的预测提名图,并探索宫颈腺癌的最佳治疗方法。研究方法本研究选择 SEER 数据库中的 2 478 例宫颈腺癌患者作为训练队列,选择大连理工大学附属肿瘤医院、辽宁肿瘤医院和研究所的 195 例宫颈腺癌患者作为外部验证队列。收集了两个队列的临床病理资料和随访数据。放疗组的定义是在初诊后接受以同步化学放疗为基础的综合治疗,而手术组的定义是接受以根治性手术为基础的综合治疗。采用对数秩检验和考克斯回归评估影响宫颈腺癌患者预后的因素。绘制了预测宫颈腺癌患者 3 年和 5 年总生存率的提名图,然后对 SEER 数据库的训练队列进行了内部验证,并对医院队列进行了外部验证。结果:(1)在 SEER 数据库训练队列中,放疗组有 385 名患者(15.54%,385/2 478),手术组有 2 093 名患者(84.46%,2 093/2 478)。放疗组患者的总生存时间为(55.8±51.3)个月,手术组患者的总生存时间为(94.4±61.7)个月,两组比较差异有统计学意义(χ2=256.44,PP50岁)、单身、肿瘤巨大(>4 cm)、病理分级高(G2、G3)、FIGO分期晚期(≥Ⅱa2期)是宫颈腺癌患者总生存时间的独立危险因素(全部PHR=0.619,95%CI:0.494-0.777;局部晚期P4~HR=0.414,95%CI:0.182-0.942;P=0.036)和Ⅲc T1~T2期(HR=0.473,95%CI:0.307-0.728;P=0.001)。(2)外部验证队列包括放疗组 39 名患者(20.00%,39/195)和手术组 156 名患者(80.00%,156/195)。放疗组患者的总生存时间为(51.7±34.3)个月,手术组患者的总生存时间为(63.1±26.6)个月(χ2=28.41,P4~HR=0.141,95%CI:0.023~0.843;P=0.032),Ⅲc T1~T2期(HR=0.184,95%CI:0.036~0.947;P=0.043)。(3)提名图的建立及内外部验证:根据多变量Cox回归模型筛选出的6个因素,建立了预测宫颈腺癌患者预后的提名图。内部和外部验证的一致性指数分别为 0.801 和 0.766,校正曲线与理想拟合线吻合良好。结论宫颈腺癌治疗的关键是对有条件根治性切除肿瘤的患者优先进行根治性手术。与同期化放疗相比,局部晚期(Ⅰb3、Ⅱa2)和Ⅲc(T1、T2)期宫颈腺癌患者可从以根治性手术为主的综合治疗中获益。本研究的提名图经内外部验证,对宫颈腺癌患者的生存预测效果良好。
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[Establishment of a prognostic nomogram and discussion on optimal treatment for cervical adenocarcinoma:a retrospective study based on SEER database and Chinese single-center data].

Objective: To establish and validate a predicting nomogram for cervical adenocarcinoma based on surveillance, epidemiology and end results (SEER) database and Chinese single-center data, and to explore the optimal treatment for cervical adenocarcinoma. Methods: This study selected 2 478 cervical adenocarcinoma patients from the SEER database as the training cohort, and 195 cervical adenocarcinoma patients from Cancer Hospital of Dalian University of Technology, Liaouing Cancer Hospital and Institute as an external validation cohort. Clinicopathological information and follow-up data of the two cohorts were collected. The radiotherapy group was defined as receiving comprehensive treatment based on concurrent chemoradiotherapy after initial diagnosis, while the surgery group was defined as receiving comprehensive treatment based on radical surgery. Log-rank test and cox regression were used to evaluate factors affecting the prognosis of cervical adenocarcinoma patients. A nomogram was drawn to predict the 3-year and 5-year overall survival rates of cervical adenocarcinoma patients, and then internal validation of the training cohort from SEER database and external validation of the hospital cohort were conducted. Results: (1) In the SEER database training cohort, there were 385 patients (15.54%, 385/2 478) in the radiotherapy group and 2 093 patients (84.46%, 2 093/2 478) in the surgery group. Overall survival time of the radiotherapy group was (55.8±51.3) months, while that of the surgery roup was (94.4±61.7) months, the difference between the two groups was statistically significant (χ2=256.44, P<0.001). Log-rank test showed that age, marital status, maximum of tumor diameters, pathological grade, International Federation of Gynecology and Obstetrics (FIGO) stage, and treatments were all significant factors affecting the overall survival time of cervical adenocarcinoma patients (all P<0.001). Multivariate Cox regression analysis showed that elder (>50 years old), single status, huge tumors (>4 cm), high pathological grades (G2, G3), and advanced FIGO stages (≥Ⅱa2 stage) were independent risk factors for the overall survival time of cervical adenocarcinoma patients (all P<0.05); compared with radiotherapy, surgery was a protective factor for the prognosis of cervical adenocarcinoma patients (HR=0.619, 95%CI: 0.494-0.777; P<0.001). Further analysis of locally advanced stage and Ⅲc stage of patients showed that surgery was a protective factor for the prognosis of cervical adenocarcinoma patients with a maximum tumor diameter >4 to <6 cm (HR=0.414, 95%CI: 0.182-0.942; P=0.036) in locally advanced stage and Ⅲc T1 to T2 stage (HR=0.473, 95%CI: 0.307-0.728; P=0.001). (2) The external validation cohort consisted of 39 patients (20.00%, 39/195) in the radiotherapy group and 156 patients (80.00%, 156/195) in the surgery group. The overall survival time of patients in the radiotherapy group was (51.7±34.3) months, while that of the surgery group was (63.1±26.6) months (χ2=28.41, P<0.001). Further analysis was conducted on locally advanced stage and Ⅲc stage patients, and multivariate Cox regression analysis was performed after propensity score matching, which showed that surgery was a protective factor for the prognosis of cervical adenocarcinoma patients with a maximum tumor diameter >4 to <6 cm in locally advanced stage (HR=0.141, 95%CI: 0.023-0.843; P=0.032) and Ⅲc T1 to T2 stage (HR=0.184, 95%CI: 0.036-0.947; P=0.043). (3) Establishment and internal and external validation of nomogram: based on the six factors screened out by the multivariate Cox regression model, the nomogram was developed to predict the prognosis of cervical adenocarcinoma patients. The consistency index of the internal and external validation were 0.801 and 0.766, respectively, and the calibration curves matched well with the ideal fitting line. Conclusions: The key to the treatment of cervical adenocarcinoma is to prioritize radical surgery for patients with conditions for radical tumor resection. Compared with concurrent chemoradiotherapy, patients with locally advanced stages (Ⅰb3, Ⅱa2), and Ⅲc (T1, T2) stages cervical adenocarcinoma could benefit from comprehensive treatment based on radical surgery. The nomogram of this study has been validated internally and externally, and show good survival prediction efficacy for cervical adenocarcinoma patients.

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