Department of Surgical Oncology (Urology), Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Int J Cancer. 2022 Dec 1;151(11):2004-2011. doi: 10.1002/ijc.34125. Epub 2022 Jun 10.
Despite treatment with cisplatin-based chemotherapy and surgical resection, clinical outcomes of patients with locally advanced urothelial carcinoma (UC) remain poor. We compared neoadjuvant/induction platinum-based combination chemotherapy (NAIC) with combination immune checkpoint inhibition (cICI). We identified 602 patients who attended our outpatient bladder cancer clinic in 2018 to 2019. Patients were included if they received NAIC or cICI for cT3-4aN0M0 or cT1-4aN1-3M0 UC. NAIC consisted of cisplatin-based chemotherapy or gemcitabine-carboplatin in case of cisplatin-ineligibility. A subset of patients (cisplatin-ineligibility or refusal of NAIC) received ipilimumab plus nivolumab in the NABUCCO-trial (NCT03387761). Treatments were compared using the log-rank test and propensity score-weighted Cox regression models. We included 107 Stage III UC patients treated with NAIC (n = 83) or cICI (n = 24). NAIC was discontinued in 11 patients due to progression (n = 6; 7%) or toxicity (n = 5; 6%), while cICI was discontinued in 6 patients (25%) after 2 cycles due to toxicity (P = .205). After NAIC, patients had surgical resection (n = 50; 60%), chemoradiation (n = 26; 30%), or no consolidating treatment due to progression (n = 5; 6%) or toxicity (n = 2; 2%). After cICI, all patients underwent resection. After resection (n = 74), complete pathological response (ypT0N0) was achieved in 11 (22%) NAIC-patients and 11 (46%) cICI-patients (P = .056). Median (IQR) follow-up was 26 (20-32) months. cICI was associated with superior progression-free survival (P = .003) and overall survival (P = .003) compared to NAIC. Our study showed superior survival in Stage III UC patients pretreated with cICI if compared to NAIC. Our findings provide a strong rationale for validation of cICI for locally advanced UC in a comparative phase-3 trial.
尽管接受了基于顺铂的化疗和手术切除,局部晚期尿路上皮癌 (UC) 患者的临床结局仍然不佳。我们比较了新辅助/诱导铂类联合化疗 (NAIC) 与联合免疫检查点抑制 (cICI)。我们确定了 2018 年至 2019 年在我们的膀胱癌门诊就诊的 602 名患者。如果患者患有 cT3-4aN0M0 或 cT1-4aN1-3M0 UC,则接受 NAIC 或 cICI。NAIC 包括基于顺铂的化疗或吉西他滨-卡铂,如果不适合顺铂。一组患者(顺铂不耐受或拒绝 NAIC)在 NABUCCO 试验中接受了 ipilimumab 加 nivolumab(NCT03387761)。使用对数秩检验和倾向评分加权 Cox 回归模型比较治疗。我们纳入了 107 名接受 NAIC(n=83)或 cICI(n=24)治疗的 III 期 UC 患者。由于进展(n=6;7%)或毒性(n=5;6%),11 名患者停止了 NAIC,而由于毒性(n=6;25%),6 名患者在 2 个周期后停止了 cICI(P=0.205)。接受 NAIC 后,患者接受了手术切除(n=50;60%)、放化疗(n=26;30%)或由于进展(n=5;6%)或毒性(n=2;2%)而未进行巩固治疗。接受 cICI 后,所有患者均接受了切除。在切除后(n=74),11 名 NAIC 患者(22%)和 11 名 cICI 患者(46%)达到完全病理缓解(ypT0N0)(P=0.056)。中位(IQR)随访时间为 26(20-32)个月。与 NAIC 相比,cICI 与无进展生存期(P=0.003)和总生存期(P=0.003)的改善相关。我们的研究表明,与 NAIC 相比,预处理接受 cICI 的 III 期 UC 患者的生存获益更高。我们的研究结果为在比较性 III 期试验中验证局部晚期 UC 的 cICI 提供了强有力的理由。