Tian Yang, Cheng Xiankui, Li Yanqing
Department of Oncology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Department of Pathology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
J Cancer Res Ther. 2020 Sep;16(5):1177-1181. doi: 10.4103/jcrt.JCRT_589_20.
Desmoplastic small round cell tumor (DSRCT) is a type of soft-tissue sarcoma with poor prognosis. Current treatments include multidisciplinary treatment options such as surgery, chemotherapy, and radiotherapy. Apatinib is an oral, small-molecule, anti-tumor, angiogenesis-targeted drug, which acts mainly on the intracellular binding site of vascular endothelial growth factor receptor-2. In this study, we administered apatinib in combination with chemotherapy to achieve good disease control. This is a 31-year-old male who presented with upper abdominal pain, nausea, and anorexia for over a month. Imaging revealed multiple solid masses and ascites in the liver and abdominal cavity. He was diagnosed as having cholangiocarcinoma with metastasis to the liver, both lungs, bone, and multiple lymph nodes in the neck, abdominal and pelvic cavity, retroperitoneum, and palpitate angle, based on a percutaneous biopsy of the liver and an abdominal mass, and other examinations. Computed tomography revealed disease progression after two cycles of gemcitabine combined with nedaplatin chemotherapy. Next-generation sequencing detection based on the Illumina high-throughput sequencing platform suggested EWSR1 exon7- Wilms tumor 1 exon8 fusion. The pathology was verified and diagnosed as DSRCT. The chemotherapy regimen was changed to cyclophosphamide, epirubicin, vincristine, and oral apatinib for two cycles. The lesions were mostly reduced, and partial response was evaluated. This case is the first report of the efficacy of apatinib combined with systemic chemotherapy in the treatment of DSRCT, which can become an alternative treatment for this disease.
促结缔组织增生性小圆细胞肿瘤(DSRCT)是一种预后较差的软组织肉瘤。目前的治疗方法包括多学科治疗方案,如手术、化疗和放疗。阿帕替尼是一种口服的小分子抗肿瘤血管生成靶向药物,主要作用于血管内皮生长因子受体-2的细胞内结合位点。在本研究中,我们给予阿帕替尼联合化疗以实现良好的疾病控制。这是一名31岁男性,出现上腹部疼痛、恶心和厌食一个多月。影像学检查显示肝脏和腹腔内有多个实性肿块及腹水。根据肝脏和腹部肿块的经皮活检及其他检查,他被诊断为胆管癌伴肝、双肺、骨转移,以及颈部、腹腔和盆腔、腹膜后及锁骨上多个淋巴结转移。计算机断层扫描显示吉西他滨联合奈达铂化疗两个周期后疾病进展。基于Illumina高通量测序平台的二代测序检测提示EWSR1外显子7-肾母细胞瘤1外显子8融合。病理检查确诊为DSRCT。化疗方案改为环磷酰胺、表柔比星、长春新碱及口服阿帕替尼,共两个周期。病变大多缩小,评估为部分缓解。该病例是阿帕替尼联合全身化疗治疗DSRCT疗效的首例报道,可为该病提供一种替代治疗方法。