Sullivan Mackenzie W, Graves Stephen, Adkoli Anusha, Zhou Qin, Iasonos Alexia, Ellenson Lora H, Chi Dennis S, Aghajanian Carol, Liu Ying L, Sonoda Yukio, O'Cearbhaill Roisin E, Weigelt Britta, Grisham Rachel N
Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Department of Obstetrics and Gynecology, Robert Wood Johnson University Hospital, New Brunswick, New Jersey, USA.
Cancer. 2025 Jan 1;131(1):e35523. doi: 10.1002/cncr.35523. Epub 2024 Aug 16.
Homologous recombination deficiency (HRD) testing is used to determine the appropriateness of poly ADP-ribose polymerase inhibitors for patients with epithelial ovarian cancer and no germline/somatic BRCA1/2 alterations. Myriad MyChoice CDx reports a genomic instability score (GIS) to quantify the level of HRD, with a positive score defined as ≥42. The authors sought to define factors associated with obtaining an inconclusive HRD test result.
GIS was retrieved for patients at their institution with epithelial ovarian cancer without germline/somatic BRCA1/2 deleterious alterations who underwent HRD testing from April 2020-August 2023. Clinical data were abstracted from the medical record.
Of 477 HRD test results identified, 57 (12%) were inconclusive. High-grade serous ovarian cancers had higher GIS than other histologic types (median 29 vs. 21, p < .001). Most HRD cases were of high-grade serous histology; no cases with clear cell or endometrioid histology were HRD-positive. On univariate analysis, interval versus primary cytoreductive surgery, other specimen sources versus surgical specimens, and chemotherapy exposure were risk factors for inconclusive HRD testing. On multivariable analysis, chemotherapy exposure, and tissue source were associated with an inconclusive test result, with surgical specimens more likely to yield a conclusive result than other sources (biopsy, cytology, other). Age, stage, self-reported race, and histology were not associated with an inconclusive result.
Surgical tissue was more likely to yield a conclusive HRD test result versus other sources of epithelial ovarian cancer tissue acquisition. When feasible, laparoscopic biopsy before initiation of neoadjuvant chemotherapy may increase the likelihood of obtaining interpretable HRD test results.
同源重组缺陷(HRD)检测用于确定聚ADP核糖聚合酶抑制剂对上皮性卵巢癌且无胚系/体细胞BRCA1/2改变患者的适用性。Myriad MyChoice CDx报告一个基因组不稳定评分(GIS)以量化HRD水平,阳性评分定义为≥42。作者试图确定与获得不确定的HRD检测结果相关的因素。
检索2020年4月至2023年8月在其机构接受HRD检测的无胚系/体细胞BRCA1/2有害改变的上皮性卵巢癌患者的GIS。临床数据从病历中提取。
在477个HRD检测结果中,57个(12%)为不确定结果。高级别浆液性卵巢癌的GIS高于其他组织学类型(中位数29对21,p<0.001)。大多数HRD病例为高级别浆液性组织学;无透明细胞或子宫内膜样组织学的病例为HRD阳性。单因素分析显示,间隔期与初次细胞减灭术、其他标本来源与手术标本以及化疗暴露是HRD检测结果不确定的危险因素。多因素分析显示,化疗暴露和组织来源与检测结果不确定相关,手术标本比其他来源(活检、细胞学、其他)更可能产生确定性结果。年龄、分期、自我报告的种族和组织学与不确定结果无关。
与其他获取上皮性卵巢癌组织的来源相比,手术组织更可能产生确定性的HRD检测结果。在可行的情况下,在新辅助化疗开始前进行腹腔镜活检可能会增加获得可解释的HRD检测结果的可能性。