Saboya Luciana, Buosi Keini, Silva Tiago, Candido Elaine, Morari Josiane, Velloso Licio A, Shariat Shahrokh F, Sadi Marcus V, Reis Leonardo O
UroScience, School of Medical Sciences, University of Campinas, Campinas, 13083-887, Brazil.
Department of Urology, Federal University of São Paulo, EPM, São Paulo, 04023-062, Brazil.
Oncol Res. 2025 May 29;33(6):1495-1503. doi: 10.32604/or.2025.061812. eCollection 2025.
To determine the safety and the role of modulating cytokines and proteases in the immune response to intravesical Bacillus Calmette-Guérin (BCG) when primed with systemic intradermal BCG.
Phase 1 and mechanistic longitudinal, prospective, single-blind randomized study (NCT04806178). Twenty-one non-muscle invasive urothelial bladder cancer patients undergoing intravesical adjuvant BCG after transurethral resection of bladder tumor (TURBT) in a teaching hospital between September 2021 and April 2023 were randomized to 0.1 mL of intradermal BCG vaccine or placebo (0.9% saline) administered 15 days before the start of intravesical BCG therapy. Blood samples were evaluated mechanistically regarding eight cytokines serum levels interferon-induced transmembrane protein 3 Gene (IFITM3), Interleukin 1 beta (IL1-BETA), interleukin-2 receptor alpha chain (IL2 RA), Interleukin 6 (IL 6), Interleukin 10 (IL 10), Tumor necrosis factor alpha (TNF-α), Interferon-β, AXL, and one protease CASPASE 8.
After 1 exclusion, twenty patients were randomized to intradermal BCG (n = 11) and intradermal placebo (n = 9). There was no difference in adverse effects emerging from the intravesical Onco-BCG therapy, and no difference in the expression of the cytokines and proteases analyzed between control and intervention, and over time.
Intradermal BCG administration before intravesical application was safe, with no increase in adverse effects. It also does not seem to change the analyzed targets during the intravesical induction-phase BCG. Other immune targets should be explored in the future. The Brazilian tuberculosis-endemic status, where BCG vaccination is mandatory, might have affected the results.
确定在全身皮内注射卡介苗(BCG)启动免疫后,调节细胞因子和蛋白酶在膀胱内卡介苗免疫反应中的安全性及作用。
1期、机制性纵向、前瞻性、单盲随机研究(NCT04806178)。2021年9月至2023年4月期间,在一家教学医院接受经尿道膀胱肿瘤切除术(TURBT)后膀胱内辅助卡介苗治疗的21例非肌层浸润性尿路上皮膀胱癌患者,被随机分为在膀胱内卡介苗治疗开始前15天给予0.1 mL皮内卡介苗疫苗或安慰剂(0.9%生理盐水)。对血液样本进行机制性评估,检测8种细胞因子血清水平,即干扰素诱导跨膜蛋白3基因(IFITM3)、白细胞介素1β(IL1-BETA)、白细胞介素-2受体α链(IL2 RA)、白细胞介素6(IL 6)、白细胞介素10(IL 10)、肿瘤坏死因子α(TNF-α)、干扰素-β、AXL,以及1种蛋白酶半胱天冬酶8(CASPASE 8)。
排除1例患者后,20例患者被随机分为皮内卡介苗组(n = 11)和皮内安慰剂组(n = 9)。膀胱内Onco-BCG治疗产生的不良反应无差异,对照组和干预组之间以及随时间推移,所分析的细胞因子和蛋白酶表达也无差异。
膀胱内应用卡介苗前皮内注射卡介苗是安全的,不良反应未增加。在膀胱内卡介苗诱导期,它似乎也不会改变所分析的靶点。未来应探索其他免疫靶点。巴西作为卡介苗接种强制实施的结核病流行地区,可能影响了研究结果。