De Cecco Loris, Bagnoli Marina, Chiodini Paolo, Pignata Sandro, Mezzanzanica Delia
Integrated Biology Platform, Department of Applied Research and Technology Development, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Molecular Therapies Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Cancers (Basel). 2021 Mar 27;13(7):1544. doi: 10.3390/cancers13071544.
Epithelial ovarian cancer (EOC) remains the second most common cause of gynecological cancer deaths. To improve patients' outcomes, we still need reliable biomarkers of early relapse, of which external independent validation is a crucial process. Our previously established prognostic signature, MiROvaR, including 35 microRNAs (miRNA) able to stratify EOC patients for their risk of relapse, was challenged on a new independent cohort of 197 EOC patients included in the Pelvic Mass Study whose miRNA profile was made publically available, thus resulting in the only accessible database aside from the EOC TCGA collection. Following accurate data matrix adjustment to account for the use of different miRNA platforms, MiROvaR confirmed its ability to discriminate early relapsing patients. The model's original cutoff separated 156 (79.2%) high- and 41 (20.8%) low-risk patients with median progression free survival (PFS) of 16.3 months and not yet reached (NYR), respectively (hazard ratio (HR): 2.42-95% Confidence Interval (CI) 1.49-3.93; Log-rank = 0.00024). The MiROvaR predictive accuracy (area under the curve (AUC) = 0.68; 95% Cl 0.57-0.79) confirms its prognostic value. This external validation in a totally independently collected, handled and profiled EOC cohort suggests that MiROvaR is a strong and reliable biomarker of EOC early relapse, warranting prospective validation.
上皮性卵巢癌(EOC)仍然是妇科癌症死亡的第二大常见原因。为了改善患者的治疗结果,我们仍然需要可靠的早期复发生物标志物,其中外部独立验证是一个关键过程。我们之前建立的预后特征MiROvaR,包括35种能够对EOC患者复发风险进行分层的微小RNA(miRNA),在盆腔肿块研究中纳入的197例EOC患者的新独立队列中进行了验证,该队列的miRNA谱已公开,这是除EOC TCGA数据集之外唯一可访问的数据库。在对数据矩阵进行准确调整以考虑不同miRNA平台的使用后,MiROvaR证实了其区分早期复发患者的能力。该模型的原始临界值将156例(79.2%)高危患者和41例(20.8%)低危患者区分开来,其无进展生存期(PFS)中位数分别为16.3个月和尚未达到(NYR)(风险比(HR):2.42 - 95%置信区间(CI)1.49 - 3.93;对数秩检验 = 0.00024)。MiROvaR的预测准确性(曲线下面积(AUC) = 0.68;95% CI 0.57 - 0.79)证实了其预后价值。在一个完全独立收集、处理和分析的EOC队列中的这种外部验证表明,MiROvaR是EOC早期复发的一个强大且可靠的生物标志物,值得进行前瞻性验证。