不同组织学亚型宫颈癌患者生存率的比较:回顾性倾向评分匹配分析

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.7150/jca.100653
Yugu Zhang, Pei Shu, Xin Wang, Ganlu Ouyang, Jitao Zhou, Yaqin Zhao, Zhiping Li, Yongsheng Wang, Yalin Shen
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引用次数: 0

摘要

研究目的研究不同组织学亚型(腺鳞癌、腺癌和鳞癌)与宫颈癌预后的相关性。材料与方法:在这项回顾性队列分析中,纳入了2009年至2018年间在四川大学华西医院接受根治术后同时接受化放疗(CCRT)或放疗(RT)的宫颈癌患者。研究纳入了病理确诊为宫颈腺鳞癌(ASC)、腺癌(AC)和鳞癌(SCC)的患者。为确保均衡代表性,在宫颈腺鳞癌(ASC)或腺癌(AC)和鳞状细胞癌(SCC)之间进行了 1:3 倾向评分匹配(PSM)。评估了不同病理亚型的预后,包括5年总生存期(OS)、5年无病生存期(DFS)以及复发和转移方面的治疗失败模式。研究结果该研究在2009年至2018年间共纳入714名患者,其中614人(86%)被确诊为SCC。在1:3比例倾向得分配对中,34例ASC与102例SCC配对,而66例AC与另外198例SCC配对。各治疗组的基线人口统计学特征和疾病特征非常均衡。在中位 41 个月(14 至 122 个月)的随访期间,共有 40 例患者复发。复发的主要模式是远处转移,40 例中有 36 例。在这些病例中,28 例(9.3%)确诊为 SCC 的患者、10 例(15.2%)确诊为 AC 的患者和 2 例(5.9%)确诊为 ASC 的患者出现了复发。在 AC 组中,分别有 2% 和 12% 的病例出现局部失败和远处失败。相比之下,配对 SCC 组的相应比例分别为 0.6% 和 8.7%。AC组的5年OS和DFS率分别为82.1%和79.2%,而配对SCC组的5年OS和DFS率分别为95.2%和92.8%(P结论:通过比较不同组织学亚型的预后结果,我们得出结论:AC组织学与预后不良和远处复发风险增加有关。ASC组织学与SCC组织学的预后相似,而非AC。鉴于在调整预后因素后,确诊为 AC 的患者预后较差,因此,除了目前的常规治疗方法外,探索其他治疗方案已成为当务之急。
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Comparison of Survival Between Different Histological Subtypes in Cervical Cancer Patients: A Retrospective and Propensity Score-matched Analysis.

Objective: To investigate the correlation between different histological subtypes (adenosquamous carcinoma, adenocarcinoma, and squamous cell carcinoma) and the prognosis of cervical cancer. Materials and Methods: In this retrospective cohort analysis, patients with cervical cancer who underwent radical surgery followed by either concurrent chemoradiotherapy (CCRT) or radiotherapy (RT) at West China Hospital of Sichuan University between 2009 and 2018 were enrolled. The study included patients with confirmed pathological diagnoses of cervical adenosquamous carcinoma (ASC), adenocarcinoma (AC), and squamous cell carcinoma (SCC). To ensure a balanced representation, 1:3 propensity score matching (PSM) between cervical adenosquamous carcinoma (ASC) or adenocarcinoma (AC) and squamous cell carcinoma (SCC) was performed. The prognosis of different pathological subtypes, including 5-year overall survival (OS), 5-year disease-free survival (DFS), and treatment failure patterns in terms of recurrence and metastasis, were evaluated between groups. Results: This study enrolled a total of 714 patients between 2009 and 2018, of whom 614 (86%) were diagnosed with SCC. In a 1:3 ratio propensity score matching, 34 cases of ASC were matched with 102 cases of SCC, while 66 cases of AC were paired with another 198 cases of SCC. Baseline demographic and disease characteristics were well-balanced among the treatment groups. During a median follow-up period of 41 months (range: 14 to 122 months), a total of 40 patients experienced disease recurrence. The primary recurrence pattern was distant metastasis, observed in 36 out of 40 cases. Among these cases, recurrence occurred in 28 patients (9.3%) diagnosed with SCC, 10 patients (15.2%) with AC, and 2 patients (5.9%) with ASC. In the AC group, local failure and distant failure were observed in 2% and 12% of cases, respectively. In comparison, the corresponding rates in the paired SCC group were 0.6% and 8.7%. The 5-year OS and DFS rates in the AC group were 82.1% and 79.2%, respectively, compared to the paired SCC group, which had rates of 95.2% and 92.8% respectively (p<0.05). Conversely, in the ASC group, the 5-year OS and DFS rates were 96.3% and 92.6%, while the paired SCC group displayed OS and DFS rates of 93.4% and 81.2% respectively, with no statistically significant difference observed. Conclusions: By comparing the prognostic outcomes of different histological subtypes, we concluded that AC histology was linked to a poor prognosis and an increased risk of distant recurrence. ASC histology had a similar outcome to SCC histology rather than AC. Given the poor prognosis for patients diagnosed with AC after adjusting for prognostic factors, it becomes imperative to explore alternative treatment options beyond the current conventional therapy for this condition.

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