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人乳头瘤病毒(HPV)非相关型与HPV相关型宫颈腺癌的差异分析

Analysis of the differences between HPV-independent and HPV-related cervical adenocarcinoma.

作者信息

He Jing, Tu Lu Weng Jiang Gulixian, Zeng Lin

机构信息

Department of Pathology, The Third Hospital of Mianyang, Mianyang, China.

Department of Critical Care Medicine, Cancer Hospital Affiliated to Xinjiang Medical University, Urumqi, China.

出版信息

Front Oncol. 2025 Apr 17;15:1544207. doi: 10.3389/fonc.2025.1544207. eCollection 2025.

Abstract

BACKGROUND

No prognostic evaluation criteria have been established for either human papillomavirus (HPV)-related cervical adenocarcinoma (HPV-CA) or HPV-independent cervical adenocarcinoma (HPV-Ind-CA). We aimed to compare and analyze the clinicopathological features and survival prognosis of patients with HPV-related and HPV-independent cervical adenocarcinoma to facilitate clinical diagnosis, treatment and survival prognosis of patients with cervical adenocarcinoma.

METHODS

Clinical data were collected from 47 patients with HPV-Ind-CA (HPV-Ind-CA group) and 285 patients with HPV-CA (HPV-CA group), who were diagnosed at the Oncology Hospital affiliated with Xinjiang Medical University between October 2012 and July 2023. A retrospective analysis was performed to compare the clinical characteristics (including age, ethnicity, fundamental diseases, initial symptoms, gynecological examination findings such as contact bleeding, menstrual history with regard to menopausal status, history of pregnancy and abortion, coexisting benign uterine lesions, etc.), tumor markers (CEA, CA125, CA199), HPV-infection(HPVI), treatment regimens (surgery, radiotherapy and chemotherapy), and pathological results (specific pathological subtype, maximum lesion diameter, degree of tumor differentiation, International Federation of Gynecology and Obstetrics [FIGO] stage) between the two groups. All patients were followed up until July 30, 2023 and differences in therapeutic efficacy (complete response, stable disease, progressive disease) and survival outcomes (progression-free survival [PFS] and overall survival [OS]) were compared between the two patient groups following treatment.

RESULTS

The proportions of patients in the HPV-Ind-CA and HPV-CA groups were 14.2% and 85.8%, respectively. Most patients presented with irregular vaginal bleeding, and a significant number experienced contact bleeding. The patients in the HPV-Ind-CA group were older (≥50 years), had a lower degree of differentiation, a later FIGO stage (> I stage), higher CA125 levels, and constituted a greater number of postmenopausal patients (P < 0.05) than those in the HPV-CA group. The median PFS and OS in the HPV-Ind-CA group were 12 ± 25.5 and 21 ± 25.1 months, respectively; the 3-year OS and PFS rates were 70.21%, and 59.57%, respectively. In contrast, the median PFS in the HPV-CA group was significantly longer at 26 ± 32.3 months, with a corresponding median OS of 35 ± 31.9 months; their respective 3-year OS and PFS rates were 80.70% and 73.68%. The HPV-Ind-CA group demonstrated significantly shorter PFS and OS than the HPV-CA group (P < 0.05). In the HPV-Ind-CA cohort, low cervical adenocarcinoma differentiation (HR=152.673, 95% CI: 1.777-13117.314, P=0.027) and high CA199 levels (HR=104.888, 95%CI: 2.420-4546.373, P=0.016) were independent prognostic factors for OS. Conversely, in the HPV-CA cohort, the FIGO stage (> stage I), absence of HPVI, and high CA125 levels were independent prognostic factors influencing both OS and PFS outcomes; additionally, older age ≥ 50 years and high CA199 levels were independent risk factors for OS and PFS, respectively. Thus, greater than stage I FIGO stage and high CA125 and CA199 levels were identified as independent prognostic factors for PFS and OS in cervical adenocarcinoma. Furthermore, the absence of HPVI and older age of ≥50 years also constituted as independent risk factors for OS in this patient population.

CONCLUSIONS

Compared with HPV-CA, HPV-Ind-CA is associated with inferior clinicopathological characteristics and survival outcomes. For patients who are HPV-negative and have elevated levels of CA125 and CA199, with a FIGO stage of I or higher, it is advisable to contemplate an intensified treatment protocol. This approach aims to enhance the opportunity for curative surgical resection when the patient's physical condition permits it, thereby improving the overall prognosis.

摘要

背景

目前尚未建立针对人乳头瘤病毒(HPV)相关宫颈腺癌(HPV-CA)或HPV非依赖性宫颈腺癌(HPV-Ind-CA)的预后评估标准。我们旨在比较和分析HPV相关和HPV非依赖性宫颈腺癌患者的临床病理特征及生存预后,以促进宫颈腺癌患者的临床诊断、治疗及生存预后评估。

方法

收集2012年10月至2023年7月在新疆医科大学附属肿瘤医院确诊的47例HPV-Ind-CA患者(HPV-Ind-CA组)和285例HPV-CA患者(HPV-CA组)的临床资料。进行回顾性分析,比较两组患者的临床特征(包括年龄、种族、基础疾病、初始症状、妇科检查结果如接触性出血、绝经状态的月经史、妊娠和流产史、并存的良性子宫病变等)、肿瘤标志物(癌胚抗原、糖类抗原125、糖类抗原199)、HPV感染情况(HPVI)、治疗方案(手术、放疗和化疗)以及病理结果(具体病理亚型、最大病变直径、肿瘤分化程度、国际妇产科联盟[FIGO]分期)。对所有患者进行随访至2023年7月30日,比较两组患者治疗后的疗效差异(完全缓解、病情稳定、病情进展)及生存结局(无进展生存期[PFS]和总生存期[OS])。

结果

HPV-Ind-CA组和HPV-CA组患者的比例分别为14.2%和85.8%。大多数患者表现为不规则阴道出血,相当一部分患者有接触性出血。与HPV-CA组相比,HPV-Ind-CA组患者年龄较大(≥50岁)、分化程度较低、FIGO分期较晚(>I期)、CA125水平较高,绝经后患者比例更大(P<0.05)。HPV-Ind-CA组的中位PFS和OS分别为12±25.5个月和21±25.1个月;3年OS率和PFS率分别为70.21%和59.57%。相比之下,HPV-CA组的中位PFS显著更长,为26±32.3个月,相应的中位OS为35±31.9个月;其3年OS率和PFS率分别为80.70%和73.68%。HPV-Ind-CA组的PFS和OS明显短于HPV-CA组(P<0.05)。在HPV-Ind-CA队列中,宫颈腺癌低分化(HR=152.673,95%CI:1.777 - 13117.314,P=0.027)和CA199水平高(HR=104.888,95%CI:2.420 - 4546.373,P=0.016)是OS的独立预后因素。相反,在HPV-CA队列中,FIGO分期(>I期)、无HPVI以及CA125水平高是影响OS和PFS结局的独立预后因素;此外,年龄≥50岁和CA199水平高分别是OS和PFS的独立危险因素。因此,FIGO分期>I期以及CA125和CA199水平高被确定为宫颈腺癌PFS和OS的独立预后因素。此外,无HPVI和年龄≥50岁也是该患者群体OS的独立危险因素。

结论

与HPV-CA相比,HPV-Ind-CA的临床病理特征和生存结局较差。对于HPV阴性、CA125和CA199水平升高且FIGO分期为I期或更高的患者,建议考虑强化治疗方案。该方法旨在当患者身体状况允许时增加根治性手术切除的机会,从而改善总体预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d55/12043462/216850bc4358/fonc-15-1544207-g001.jpg

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