Apolo Andrea B, Atiq Saad, Kydd Andre R, Chelluri Raju, Millan Braden, Gurram Sandeep, Chandran Elias, Simon Nicholas
Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Cancer. 2025 Aug 15;131(16):e70020. doi: 10.1002/cncr.70020.
Looking back at 2024, the authors highlight the top five clinical advances in bladder cancer (urothelial carcinoma), from: (1) novel drug-delivery mechanisms in intravesical therapy for nonmuscle-invasive bladder cancer and muscle-invasive bladder cancer (MIBC); (2) immune checkpoint inhibition (ICI) as adjuvant and (3) perioperative therapy in MIBC; (4) circulating tumor DNA as a biomarker in MIBC; to (5) a new standard of care in first-line metastatic urothelial carcinoma. TAR-200 is a new intravesical drug-delivery system that enables controlled release of gemcitabine but may be used with other anticancer drugs to treat nonmuscle-invasive bladder cancer and MIBC. Two phase 3 studies of adjuvant ICI (nivolumab and pembrolizumab) have both reported a doubling of disease-free survival in patients with high-risk MIBC receiving therapy. Perioperative durvalumab, including neoadjuvant therapy plus gemcitabine and cisplatin before radical cystectomy followed by adjuvant durvalumab, demonstrated an improvement in event-free survival and overall survival for patients with MIBC. Circulating tumor DNA is a promising biomarker to select patients with MIBC for adjuvant ICI therapy. Finally, the combination of enfortumab vedotin, an antibody-drug conjugate, plus pembrolizumab doubled overall survival compared with standard gemcitabine plus platinum in patients with metastatic urothelial carcinoma and has been implemented in treatment guidelines in the United States, Europe, and Asia as the new standard of care in this setting, transforming the treatment landscape for bladder cancer.
回顾2024年,作者重点介绍了膀胱癌(尿路上皮癌)的五大临床进展,包括:(1)非肌层浸润性膀胱癌和肌层浸润性膀胱癌(MIBC)膀胱内治疗中的新型药物递送机制;(2)免疫检查点抑制(ICI)作为辅助治疗以及(3)MIBC的围手术期治疗;(4)循环肿瘤DNA作为MIBC的生物标志物;以及(5)一线转移性尿路上皮癌的新护理标准。TAR-200是一种新型膀胱内药物递送系统,可实现吉西他滨的控释,但也可与其他抗癌药物联合使用,用于治疗非肌层浸润性膀胱癌和MIBC。两项辅助ICI(纳武单抗和帕博利珠单抗)的3期研究均报告称,接受治疗的高危MIBC患者无病生存期翻倍。围手术期使用度伐利尤单抗,包括在根治性膀胱切除术前行新辅助治疗加吉西他滨和顺铂,术后再行辅助度伐利尤单抗治疗,结果显示MIBC患者的无事件生存期和总生存期均有所改善。循环肿瘤DNA是一种很有前景的生物标志物,可用于选择适合接受辅助ICI治疗的MIBC患者。最后,抗体药物偶联物恩杂鲁胺与帕博利珠单抗联合使用,与标准的吉西他滨加铂类药物相比,转移性尿路上皮癌患者的总生存期翻倍,并且在美国、欧洲和亚洲的治疗指南中已将其作为这种情况下的新护理标准,改变了膀胱癌的治疗格局。