University of British Columbia, Vancouver, Canada.
SWOG Statistical Center, Seattle, WA, USA.
Eur Urol. 2023 Dec;84(6):536-544. doi: 10.1016/j.eururo.2023.08.004. Epub 2023 Aug 16.
Although radical cystectomy (RC) is the standard of care for patients with bacillus Calmette-Guérin (BCG)-unresponsive high-risk non-muscle-invasive bladder cancer (NMIBC), many patients are ineligible for surgery or elect bladder preservation.
To evaluate the efficacy and safety of atezolizumab in BCG-unresponsive high-risk NMIBC.
DESIGN, SETTING, AND PARTICIPANTS: This was a single-arm phase 2 trial in patients with BCG-unresponsive high-risk NMIBC who were ineligible for or declined RC.
Intravenous atezolizumab every 3 wk for 1 yr.
The primary endpoint was the pathological complete response (CR) rate for patients with carcinoma in situ (CIS) determined via mandatory biopsy at 6 mo. Event-free survival (EFS) at 18 mo for patients with non-CIS tumors and treatment-related adverse events (TRAEs) were key secondary endpoints.
Of 172 patients enrolled in the trial, 166 received at least one dose of atezolizumab (safety analysis) and 129 were eligible (efficacy analysis). Of the 74 patients with CIS, 20 (27%) experienced a CR at 6 mo. The median duration of response was 17 mo, and 56% (95% confidence interval [CI] 34-77%) of the responses were durable to at least 12 mo. The 18-mo actuarial EFS rate among 55 patients with Ta/T1 disease was 49% (90% CI 38-60%). Twelve of 129 eligible patients experienced progression to muscle-invasive or metastatic disease. Grade 3-5 TRAEs occurred in 26 patients (16%), including three treatment-related deaths. The study was limited by the small sample size and a high rate of patient ineligibility.
The efficacy of atezolizumab observed among patients with BCG-unresponsive NMIBC is similar to results from similar trials with other agents, but did not meet the prespecified efficacy threshold. Modest efficacy needs to be balanced with a significant rate of TRAEs and the risk of disease progression when considering systemic immunotherapy in early-stage bladder cancer.
We tested intravenous immunotherapy (atezolizumab) in patients with high-risk non-muscle-invasive bladder cancer that recurred after BCG (bacillus Calmette-Guérin) treatment. Although we found similar outcomes to previous trials, the benefit of this therapy is modest and needs to be carefully balanced with the significant risk of side effects. This trial is registered on ClinicalTrials.gov as NCT02844816.
尽管根治性膀胱切除术(RC)是卡介苗(BCG)无应答高危非肌肉浸润性膀胱癌(NMIBC)患者的标准治疗方法,但许多患者不符合手术条件或选择保留膀胱。
评估阿替利珠单抗在 BCG 无应答高危 NMIBC 中的疗效和安全性。
设计、地点和参与者:这是一项在不符合 RC 条件或拒绝 RC 的 BCG 无应答高危 NMIBC 患者中进行的单臂 2 期试验。
静脉注射阿替利珠单抗,每 3 周 1 次,共 1 年。
主要终点是 6 个月时通过强制性活检确定的原位癌(CIS)患者的病理完全缓解(CR)率。非 CIS 肿瘤患者的无事件生存(EFS)和治疗相关不良事件(TRAEs)为关键次要终点。
在这项试验中,172 名患者中,166 名至少接受了 1 剂阿替利珠单抗(安全性分析),129 名符合条件(疗效分析)。在 74 名 CIS 患者中,20 名(27%)在 6 个月时发生 CR。中位缓解持续时间为 17 个月,56%(95%置信区间[CI]34-77%)的缓解至少持续 12 个月。55 例 Ta/T1 疾病患者的 18 个月估计 EFS 率为 49%(90%CI38-60%)。129 名符合条件的患者中有 12 名进展为肌层浸润或转移性疾病。26 名患者(16%)发生 3-5 级 TRAE,包括 3 例与治疗相关的死亡。该研究受到样本量小和患者不符合条件率高的限制。
在 BCG 无应答 NMIBC 患者中观察到的阿替利珠单抗疗效与其他药物类似试验的结果相似,但未达到预设的疗效阈值。在考虑早期膀胱癌的全身免疫治疗时,适度的疗效需要与 TRAE 的发生率和疾病进展的风险相平衡。
我们在卡介苗(BCG)治疗后复发的高危非肌肉浸润性膀胱癌患者中测试了静脉免疫治疗(阿替利珠单抗)。尽管我们发现了与以前的试验相似的结果,但这种疗法的益处是适度的,需要与显著的副作用风险仔细平衡。这项试验在 ClinicalTrials.gov 上注册为 NCT02844816。