Senguttuvan Rosemary Noel, Wei Christina, Raoof Mustafa, Dellinger Thanh H, Wang Edward Wenge
Department of Surgery, City of Hope Comprehensive Cancer Center (COH), Duarte, CA 91010, USA.
Department of Pathology, City of Hope Comprehensive Cancer Center (COH), Duarte, CA 91010, USA.
J Clin Med. 2023 Jun 4;12(11):3839. doi: 10.3390/jcm12113839.
Treatment for endometrial cancer is rapidly evolving with the increased use and integration of somatic tumor RNA sequencing in clinical practice. There is a paucity of data regarding PARP inhibition in endometrial cancer given that mutations in homologous recombination genes are rare, and currently no FDA approval exists. A 50-year-old gravida 1 para 1 woman with a diagnosis of stage IVB poorly differentiated endometrioid endometrial adenocarcinoma presented to our comprehensive cancer center. Following surgical staging, she was placed on adjuvant chemotherapy with carboplatin/paclitaxel which was held multiple times due to poor performance status and complications. CT scan of the abdomen and pelvis following cycles 3 of adjuvant chemotherapy showed recurrent progressive disease. She received one cycle of liposomal doxorubicin but discontinued it due to severe cutaneous toxicity. Based on the BRIP1 mutation identified, the patient was placed on compassionate use of Olaparib in January 2020. Imaging during this surveillance period showed a significant decrease in hepatic, peritoneal, and extraperitoneal metastases, and eventually the patient had a clinical complete response in a year. The most recent CT A/P in December 2022 showed no sites of active recurrent or metastatic disease in the abdomen or pelvis. We present a unique case of a patient with recurrent stage IVB poorly differentiated endometrioid endometrial adenocarcinoma with multiple somatic gene mutations including BRIP1, who had a pathologic complete response following compassionate use of Olaparib for 3 years. To our knowledge, this is the first reported case of high grade endometrioid endometrial cancer that has shown a pathologic complete response to a PARP inhibitor.
随着体细胞肿瘤RNA测序在临床实践中的更多应用和整合,子宫内膜癌的治疗正在迅速发展。鉴于同源重组基因的突变很少见,关于PARP抑制在子宫内膜癌中的数据很少,目前FDA尚未批准。一名50岁、孕1产1的女性被诊断为IVB期低分化子宫内膜样腺癌,就诊于我们的综合癌症中心。手术分期后,她接受了卡铂/紫杉醇辅助化疗,但由于身体状况差和并发症,化疗多次中断。辅助化疗第3周期后进行的腹部和盆腔CT扫描显示疾病复发进展。她接受了一个周期的脂质体阿霉素治疗,但由于严重的皮肤毒性而停药。基于所发现的BRIP1突变,该患者于2020年1月开始接受奥拉帕利的同情用药。在此监测期的影像学检查显示肝脏、腹膜和腹膜外转移灶显著减少,最终患者在一年内实现了临床完全缓解。2022年12月的最新CT A/P显示腹部或盆腔无活动性复发或转移病灶。我们报告了一例独特的病例,一名IVB期复发的低分化子宫内膜样腺癌患者,有包括BRIP1在内的多个体细胞基因突变,在同情使用奥拉帕利3年后实现了病理完全缓解。据我们所知,这是首例报道的高级别子宫内膜样腺癌对PARP抑制剂显示出病理完全缓解的病例。