Puty Taynah C, França Tiago G, Oliveira Paula B T, Carvalho Luís Eduardo W, Yamaguchi Nise H
Education and Research Department, Oncológica Brasil - Education and Research, Belém, Pará 66053-000, Brazil.
Biological and Health Sciences Department, University of Para, Belém, Pará 66087-662, Brazil.
Mol Clin Oncol. 2020 Aug;13(2):191-194. doi: 10.3892/mco.2020.2067. Epub 2020 Jun 10.
Sarcomas are an unusual group of tumors, accounting for ~1% of cancer in adults. Immunotherapy has been shown to be a potential therapeutic option for the management of patients with cancer. However, there is still insufficient information on the action of immunotherapy on sarcomas. A 16-year-old male patient, diagnosed in December 2013 with grade III soft-tissue sarcoma in the right arm, was admitted to a private oncology service after relapse following surgical treatment. The patient underwent chemotherapy with ifosfamide plus adriamycin for 4 cycles, associated with adjuvant radiotherapy, followed by a new resection to remove the residual lesion. A year later, imaging tests identified pulmonary micronodules, and a new resection was performed. After immunohistochemical evaluation of biopsy, a large presence of programmed cell death 1 ligand 1 (PD-L1) marker was identified in tumor tissue and immunotherapy with nivolumab was performed. At present, the patient is in immunotherapeutic treatment (42 cycles), presenting an excellent general condition and without any symptoms, and a decrease in neoplastic lung masses. The literature recommends three cycles of anthracycline plus ifosfamide as adjuvant therapy to surgical treatment. Combined surgery plus adjuvant therapy has shown benefits in malignant tumors. Immunotherapy is an important therapeutic option for soft-tissue sarcomas with high programmed cell death protein 1 (PD-1)/PD-L1 expression. Treatment for high grade soft tissue sarcoma (STS) is still limited, due to tumor heterogeneity, and further studies are needed to consolidate the possibility of using immunotherapy to treat these neoplasms. When significant levels of specific biomarkers are present in tumor tissue, immunotherapy may be beneficial as shown by the present case report.
肉瘤是一类特殊的肿瘤,约占成人癌症的1%。免疫疗法已被证明是治疗癌症患者的一种潜在治疗选择。然而,关于免疫疗法对肉瘤作用的信息仍然不足。一名16岁男性患者,于2013年12月被诊断为右臂III级软组织肉瘤,在手术治疗后复发,入住一家私立肿瘤科室。该患者接受了异环磷酰胺加阿霉素化疗4个周期,并联合辅助放疗,随后再次切除以清除残留病灶。一年后,影像学检查发现肺部微小结节,遂再次进行切除。活检经免疫组化评估后,在肿瘤组织中发现大量程序性细胞死亡1配体1(PD-L1)标志物,并对患者进行了纳武单抗免疫治疗。目前,该患者正在接受免疫治疗(42个周期),总体状况良好,无任何症状,肺部肿瘤肿块缩小。文献推荐蒽环类药物加异环磷酰胺三个周期作为手术治疗的辅助疗法。手术联合辅助疗法已显示出对恶性肿瘤有益。免疫疗法是治疗程序性细胞死亡蛋白1(PD-1)/PD-L1高表达软组织肉瘤的重要治疗选择。由于肿瘤异质性,高级别软组织肉瘤(STS)的治疗仍然有限,需要进一步研究以巩固使用免疫疗法治疗这些肿瘤的可能性。如本病例报告所示,当肿瘤组织中存在显著水平的特定生物标志物时,免疫疗法可能有益。