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.
Gynecol Oncol. 2022 Oct;167(1):107-114. doi: 10.1016/j.ygyno.2022.07.028. Epub 2022 Jul 30.
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.
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.
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.
ctHPV DNA is a promising prognostic biomarker in locally advanced cervical cancer that should be studied further for clinical use.
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。
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。
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。
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。