Han Yaqian, Zhou Yujuan, Wu Zheng, Liu Lin, Han Chen
Department of Radiation Oncology, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, PR China.
Heliyon. 2024 Sep 26;10(19):e38518. doi: 10.1016/j.heliyon.2024.e38518. eCollection 2024 Oct 15.
Urothelial carcinoma with trophoblastic differentiation represents an uncommon and aggressive malignancy for which there is currently no established standard treatment. Systemic chemotherapy as the main treatment has limited efficacy. However, recent research has demonstrated significant improvements in patient survival with the use of immune checkpoint inhibitors and antibody-drug conjugates. To our knowledge, this case represents the first successful application of an immune checkpoint inhibitor (Tislelizumab) combined with human epidermal growth factor receptor 2-targeting antibody-drug conjugate (Disitamab vedotin) in the treatment of advanced urothelial carcinoma with trophoblastic differentiation.
We describe the case of a 36-year-old male patient diagnosed with urothelial carcinoma with trophoblastic differentiation, showing high expression of programmed death-ligand 1. Tumor progression occurred after six cycles of Tislelizumab combined with chemotherapy (gemcitabine and cisplatin) followed by five cycles of Tislelizumab monotherapy. Re-biopsy confirmed metastatic urothelial carcinoma with trophoblastic differentiation, now with epidermal growth factor receptor 2 overexpression. Treatment with Disitamab vedotin in combination with Tislelizumab resulted in a biochemical and imaging complete response, leading to an overall survival exceeding 24 months. Notably, no grade 3 or 4 adverse events were observed during treatment.
The prognosis of advanced urothelial carcinoma with trophoblastic differentiation is unfavorable, and the available therapeutic options are limited. Combining Tislelizumab with Disitamab vedotin presents a promising anti-tumor strategy that warrants further investigation.
具有滋养层分化的尿路上皮癌是一种罕见且侵袭性强的恶性肿瘤,目前尚无既定的标准治疗方法。以全身化疗为主的治疗效果有限。然而,最近的研究表明,使用免疫检查点抑制剂和抗体药物偶联物可显著提高患者生存率。据我们所知,本病例代表了免疫检查点抑制剂(替雷利珠单抗)联合人表皮生长因子受体2靶向抗体药物偶联物(迪西他单抗维泊妥珠单抗)首次成功应用于治疗晚期具有滋养层分化的尿路上皮癌。
我们描述了一名36岁男性患者的病例,该患者被诊断为具有滋养层分化的尿路上皮癌,程序性死亡配体1高表达。在替雷利珠单抗联合化疗(吉西他滨和顺铂)六个周期后,接着进行五个周期的替雷利珠单抗单药治疗后出现肿瘤进展。再次活检证实为转移性具有滋养层分化的尿路上皮癌,此时表皮生长因子受体2过表达。迪西他单抗维泊妥珠单抗联合替雷利珠单抗治疗导致生化和影像学完全缓解,总生存期超过24个月。值得注意的是,治疗期间未观察到3级或4级不良事件。
晚期具有滋养层分化的尿路上皮癌预后不佳,可用的治疗选择有限。替雷利珠单抗与迪西他单抗维泊妥珠单抗联合使用是一种有前景的抗肿瘤策略,值得进一步研究。