Sui Chengxu, Wu Jie, Mei Dan, Pan Evenki, Yang Peng, Wu Tingting, Ma Yutong, Ou Qiuxiang, Song Lei
Department of Intervention Therapy, The Second Hospital of Dalian Medical University, Dalian, China.
Geneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, China.
Front Oncol. 2022 Jul 28;12:797275. doi: 10.3389/fonc.2022.797275. eCollection 2022.
Perivascular epithelioid cell tumors (PEComas) are extremely rare mesenchymal neoplasms for which the uterus is the most common site. The prognosis of malignant PEComa is poor as it is characterized by resistance to classical chemotherapies. Both mTOR inhibitors and VEGFR inhibitors exhibited clinical utility in treating malignant PEComas, but the combination of these two regimens has rarely been reported. In the present case, a uterine PEComa patient developed lung and bone metastases after the failure of chemotherapies and derived benefit from the combination regimen of an mTOR inhibitor (everolimus) and a VEGFR inhibitor (apatinib), achieving a 15-month progression-free survival. Targeted NGS revealed and mutations in the patient's primary uterine tumors and plasma ctDNA at disease progression. Plasma ctDNA clearance was consistent with a radiologic partial response determined by RECIST 1.1 and a reduction of neuron-specific enolase (NSE) and cancer antigen 125 (CA125) levels. Thus, we provided clinical evidence supporting the administration of combined therapy of mTOR and VEGFR inhibitors to metastatic uterine PEComa patients and highlighted the application of serial plasma ctDNA profiling for dynamic disease monitoring.
血管周上皮样细胞肿瘤(PEComas)是极为罕见的间质性肿瘤,其中子宫是最常见的发病部位。恶性PEComa的预后较差,其特点是对传统化疗耐药。mTOR抑制剂和VEGFR抑制剂在治疗恶性PEComas中均显示出临床应用价值,但这两种治疗方案的联合应用鲜有报道。在本病例中,一名子宫PEComa患者在化疗失败后出现肺和骨转移,并从mTOR抑制剂(依维莫司)和VEGFR抑制剂(阿帕替尼)的联合治疗方案中获益,实现了15个月的无进展生存期。靶向二代测序(NGS)显示,在疾病进展时,患者原发性子宫肿瘤和血浆循环肿瘤DNA(ctDNA)中存在 和 突变。血浆ctDNA清除与根据实体瘤疗效评价标准(RECIST)1.1确定的放射学部分缓解以及神经元特异性烯醇化酶(NSE)和癌抗原125(CA125)水平降低相一致。因此,我们提供了临床证据,支持对转移性子宫PEComa患者采用mTOR和VEGFR抑制剂联合治疗,并强调了连续血浆ctDNA分析在动态疾病监测中的应用。