The utility of the novel biomarker HE4 for monitoring epithelial ovarian cancer during PARP inhibitor treatment.

IF 4.7 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Alexandra Morell, Anne Stoklosa, Alexandra Blackman, Youngeun Armbuster, Rachael Rowswell-Turner, M Craig Miller, Richard G Moore
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引用次数: 0

Abstract

Objective: Poly(ADP-ribose) polymerase (PARP) inhibitor maintenance therapy is commonly used in patients with ovarian cancer. Prior studies have reported that serum cancer antigen 125 (CA125) poorly predicts disease progression for patients on PARP inhibitors. Human epididymal protein 4 (HE4) is a serum biomarker cleared by the United States (US) Food and Drug Administration (FDA) for monitoring disease in patients with ovarian cancer. The objective of this study was to assess the utility of serum HE4 levels as a biomarker for monitoring patients on PARP inhibitors and to compare HE4 performance parameters to those of serum CA125 levels.

Methods: A retrospective chart review was performed evaluating patients on PARP inhibitors for ovarian cancer. Patients were included if they received a PARP inhibitor for at least 2 months and had at least 3 serial serum HE4 measurements during treatment. Changes in the serum CA125 and HE4 levels between measurements and over time were calculated and correlated with disease status. The null hypothesis was that HE4 was inferior to CA125.

Results: A total of 102 patients with 103 treatment periods and 1554 evaluable serum samples were evaluated. Of these patients, 55 (53.9%) experienced a change in disease status while receiving PARP inhibitor treatment. An analysis using increases from serum baselines of ≥25.0% for HE4 and ≥15.0% for CA125 to indicate a change in disease status showed the accuracy of HE4 was 89.4% compared to 79.1% for CA125 (p < .001), indicating HE4 is not inferior to CA125 for monitoring disease status. Concordance comparison of HE4 accuracy over CA125 was 1.130 (McNemar's test p < .001), again indicating HE4 was not inferior to CA125. HE4 was shown not to be inferior to CA125 for monitoring patients with ovarian cancer on PARP inhibitors. An analysis using an increase from baseline of ≥25% for HE4 provided the highest accuracy for monitoring patients on PARP inhibitors.

新型生物标志物HE4在PARP抑制剂治疗期间监测上皮性卵巢癌的效用。
目的:聚(adp -核糖)聚合酶(PARP)抑制剂维持治疗是卵巢癌患者常用的治疗方法。先前的研究报道,血清癌抗原125 (CA125)不能预测PARP抑制剂患者的疾病进展。人附睾蛋白4 (HE4)是美国食品和药物管理局(FDA)批准用于卵巢癌患者疾病监测的血清生物标志物。本研究的目的是评估血清HE4水平作为监测PARP抑制剂患者的生物标志物的效用,并将HE4性能参数与血清CA125水平进行比较。方法:回顾性分析卵巢癌患者使用PARP抑制剂的情况。如果患者接受PARP抑制剂治疗至少2个月,并且在治疗期间至少有3次连续血清HE4测量,则纳入患者。计算血清CA125和HE4水平在测量之间和随时间的变化,并与疾病状态相关。原假设为HE4低于CA125。结果:共评估102例患者,103个治疗期,1554份可评估血清样本。在这些患者中,55例(53.9%)在接受PARP抑制剂治疗时经历了疾病状态的改变。一项使用血清基线HE4≥25.0%和CA125≥15.0%来指示疾病状态变化的分析显示,HE4的准确率为89.4%,而CA125的准确率为79.1% (p < 0.001),表明HE4在监测疾病状态方面并不低于CA125。HE4准确度与CA125的一致性比较为1.130 (McNemar检验p < .001),再次表明HE4并不逊于CA125。在监测PARP抑制剂治疗的卵巢癌患者时,HE4并不逊于CA125。一项使用HE4从基线增加≥25%的分析为监测PARP抑制剂患者提供了最高的准确性。
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来源期刊
CiteScore
6.60
自引率
10.40%
发文量
280
审稿时长
3-6 weeks
期刊介绍: The International Journal of Gynecological Cancer, the official journal of the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology, is the primary educational and informational publication for topics relevant to detection, prevention, diagnosis, and treatment of gynecologic malignancies. IJGC emphasizes a multidisciplinary approach, and includes original research, reviews, and video articles. The audience consists of gynecologists, medical oncologists, radiation oncologists, radiologists, pathologists, and research scientists with a special interest in gynecological oncology.
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