Huang Xiaotong, Wang Xuan, He Zihe, Huang Yishu, Hu Bing, Chen Weiying, Du Haifang
Second Affiliated Hospital (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou University of Chinese Medicine, Guangzhou, China.
Zhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan, China.
Cancer Med. 2025 Sep;14(18):e71243. doi: 10.1002/cam4.71243.
Bacillus Calmette-Guérin (BCG) is the standard adjuvant therapy for high-risk non-muscle invasive bladder cancer (NMIBC), yet treatment failure occurs in 30% to 40% of patients. Those with BCG-unresponsive disease face a high risk of progression and represent a critical unmet need in urologic oncology. This review summarizes the mechanisms of BCG failure and evaluates emerging therapies for BCG-unresponsive NMIBC.
We conducted a comprehensive literature review of clinical trials and preclinical studies through August 2025, focusing on therapeutic strategies for BCG-unresponsive NMIBC. Mechanisms of BCG resistance, regulatory definitions, and results from recent Phase II/III trials were analyzed.
Multiple novel therapies have demonstrated efficacy in BCG-unresponsive patients. Immune checkpoint inhibitors (e.g., pembrolizumab) achieved complete response (CR) rates of 41% in carcinoma in situ (CIS) patients. Gene therapies such as nadofaragene firadenovec and CG0070 induced CR rates of 51% and 75%, respectively. Device-assisted therapies including hyperthermic intravesical chemotherapy (HIVEC) showed 24-month recurrence-free survival of 57.4%. The IL-15 superagonist Anktiva (nogapendekin alfa inbakicept), recently FDA-approved, achieved a 71% CR rate with a median duration of 26.6 months when combined with BCG.
The treatment landscape for BCG-unresponsive NMIBC is rapidly evolving, with immune checkpoint inhibitors, gene therapies, targeted agents, and advanced drug delivery systems showing promising efficacy. These innovations provide bladder-preserving options for patients ineligible for radical cystectomy. Future directions include biomarker-driven therapy selection, combination regimens, and optimized intravesical delivery platforms to improve long-term outcomes.
卡介苗(BCG)是高危非肌层浸润性膀胱癌(NMIBC)的标准辅助治疗方法,但30%至40%的患者会出现治疗失败。那些对BCG无反应的疾病患者面临着很高的进展风险,是泌尿外科肿瘤学中一个关键的未满足需求。本综述总结了BCG治疗失败的机制,并评估了针对对BCG无反应的NMIBC的新兴疗法。
我们对截至2025年8月的临床试验和临床前研究进行了全面的文献综述,重点关注对BCG无反应的NMIBC的治疗策略。分析了BCG耐药机制、监管定义以及近期II/III期试验的结果。
多种新型疗法已在对BCG无反应的患者中显示出疗效。免疫检查点抑制剂(如帕博利珠单抗)在原位癌(CIS)患者中的完全缓解(CR)率达到41%。诸如纳多福韦基因腺病毒载体和CG0070等基因疗法分别诱导出51%和75%的CR率。包括热灌注膀胱内化疗(HIVEC)在内的设备辅助疗法显示24个月无复发生存率为57.4%。最近获得美国食品药品监督管理局(FDA)批准的IL-15超级激动剂Anktiva(诺加彭德金α因巴克西普)与BCG联合使用时,CR率达到71%,中位持续时间为26.6个月。
对BCG无反应的NMIBC的治疗格局正在迅速演变,免疫检查点抑制剂、基因疗法、靶向药物和先进的给药系统显示出有前景的疗效。这些创新为不符合根治性膀胱切除术条件的患者提供了保留膀胱的选择。未来的方向包括生物标志物驱动的治疗选择、联合方案以及优化的膀胱内给药平台,以改善长期疗效。