Wu Yinhang, Gao Yongsheng, Dou Xue, Yue Jinbo
Department of Radiation Oncology, Shandong Cancer Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, People's Republic of China.
Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.
Onco Targets Ther. 2020 Aug 12;13:8049-8054. doi: 10.2147/OTT.S264347. eCollection 2020.
A 63-year-old man with a significantly high prostate-specific antigen level was diagnosed via pathology to have advanced prostate adenocarcinoma due to multiple lung metastases. He was then treated with androgen deprivation therapy (ADT) comprising bicalutamide and goserelin. Only after 6 months of stable disease, the cancer progressed and the drug was changed to abiraterone; however, no significant therapeutic effect was observed and the disease was considered as castration-resistant prostate cancer. The histopathologic analysis of the biopsied metastatic lymph node confirmed small-cell neuroendocrine carcinoma, and genetic testing revealed BRCA1 germ-line mutation. The oral PARP inhibitor olaparib was used and achieved a partial tumor response over a period of 2.5 months. Meanwhile, palliative radiotherapy was performed for pain control in the sacrococcygeal region with complete symptom relief. The combination chemotherapy strategy of etoposide and cisplatin was used after the failure of olaparib and achieved pain alleviation in the left leg. The patient received one cycle of this chemotherapy strategy and eventually died of a rapid tumor progression, respiratory failure, and heart failure on April 27, 2019.
一名63岁男性,前列腺特异性抗原水平显著升高,经病理诊断为晚期前列腺腺癌伴多发肺转移。随后他接受了由比卡鲁胺和戈舍瑞林组成的雄激素剥夺治疗(ADT)。仅在疾病稳定6个月后,癌症进展,药物更换为阿比特龙;然而,未观察到明显治疗效果,疾病被认为是去势抵抗性前列腺癌。对活检的转移淋巴结进行组织病理学分析证实为小细胞神经内分泌癌,基因检测显示BRCA1种系突变。使用口服PARP抑制剂奥拉帕利,在2.5个月的时间内实现了部分肿瘤缓解。同时,为控制骶尾部疼痛进行了姑息性放疗,症状完全缓解。奥拉帕利治疗失败后,采用依托泊苷和顺铂联合化疗方案,左腿疼痛得到缓解。患者接受了一个周期的该化疗方案,最终于2019年4月27日死于肿瘤快速进展、呼吸衰竭和心力衰竭。