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循环游离肿瘤人乳头瘤病毒 DNA 是宫颈癌有前途的生物标志物。

Circulating cell-free tumor human papillomavirus DNA is a promising biomarker in cervical cancer.

机构信息

Department of Molecular Medicine and Surgery, Karolinska Institutet, 171 76 Stockholm, Sweden.

Department of Women's and Children's Health, Karolinska Institutet, Department of Gynaecologic Cancer, Theme Cancer, Karolinska University Hospital, SE-17176 Stockholm, Sweden.

出版信息

Gynecol Oncol. 2022 Oct;167(1):107-114. doi: 10.1016/j.ygyno.2022.07.028. Epub 2022 Jul 30.

Abstract

OBJECTIVES

Tumor cells release fragments of their DNA into the circulation, so called cell-free tumor DNA (ctDNA) or liquid biopsy. Here, we analyze if cell-free human papillomavirus DNA (ctHPV DNA) is detectable before, during and after treatment, in patients with cervical cancer or pre-malignant lesions that may develop into cervical cancer, and whether ctHPV DNA levels were correlated to patient or tumor characteristics and outcome. Furthermore, total cell-free DNA load is studied using cfAlbumin DNA as a surrogate marker.

METHODS

18 patients with locally advanced CC (LACC), 15 patients with early stage CC (ESCC) and 21 patients with pre-malignant lesions, all with verified HPV16, 18 or 45-positive lesions, were included. Pre- during- and post-treatment plasma were tested for HPV16, 18 & 45 and total cfDNA load using droplet digital PCR.

RESULTS

ctHPV DNA was found in 94.4% and 26.7% of pre-treatment plasma of patients with LACC and ESCC respectively, while all samples from patients with pre-malignant lesions were negative. Higher levels of ctHPV DNA were correlated to higher FIGO2018 stage. Patients with LACC and persistent ctHPV DNA at end-of-treatment had significantly worse progression-free survival (PFS) than patients who had cleared the ctHPV DNA (p = 0.007). Patients with total ctDNA-levels above median in pre-treatment plasma had a worse PFS (p = 0.026), compared to patients with total ctDNA-levels below median.

CONCLUSION

ctHPV DNA is a promising prognostic biomarker in locally advanced cervical cancer that should be studied further for clinical use.

摘要

目的

肿瘤细胞会将其 DNA 的片段释放到血液中,即所谓的无细胞肿瘤 DNA(ctDNA)或液体活检。在此,我们分析了在患有宫颈癌或可能发展为宫颈癌的癌前病变的患者中,治疗前、治疗中和治疗后是否可检测到游离人乳头瘤病毒 DNA(ctHPV DNA),以及 ctHPV DNA 水平是否与患者或肿瘤特征和结果相关。此外,还使用 cfAlbumin DNA 作为替代标志物来研究总游离 DNA 负荷。

方法

纳入 18 例局部晚期宫颈癌(LACC)患者、15 例早期宫颈癌(ESCC)患者和 21 例癌前病变患者,所有患者均经证实 HPV16、18 或 45 阳性病变。使用液滴数字 PCR 检测治疗前、治疗中和治疗后血浆中的 HPV16、18 和 45 以及总 cfDNA 负荷。

结果

LACC 和 ESCC 患者治疗前血浆中的 ctHPV DNA 分别有 94.4%和 26.7%检出,而所有癌前病变患者的样本均为阴性。较高水平的 ctHPV DNA 与较高的 FIGO2018 分期相关。治疗结束时持续存在 ctHPV DNA 的 LACC 患者与清除 ctHPV DNA 的患者相比,无进展生存期(PFS)显著更差(p = 0.007)。治疗前血浆中总 ctDNA 水平高于中位数的患者 PFS 更差(p = 0.026),而总 ctDNA 水平低于中位数的患者则不然。

结论

ctHPV DNA 是局部晚期宫颈癌有前途的预后生物标志物,应进一步研究用于临床。

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