Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, OH.
Cleveland Clinic Lerner College of Medicine, Cleveland, OH.
Urology. 2022 Oct;168:137-142. doi: 10.1016/j.urology.2022.06.012. Epub 2022 Jun 28.
To compare pathologic and survival outcomes between primary muscle invasive (pMIBC) and secondary muscle invasive (sMIBC) bladder cancer patients who were treated with or without cisplatin-based neoadjuvant chemotherapy (NAC) followed by radical cystectomy (RC).
We reviewed cT2-T4/N0 MIBC patients at our institution between 2010-2019. pMIBC was defined as presenting with > cT2 disease on initial or restaging TURBT with no prior history of bladder cancer. sMIBC was defined as prior history of NMIBC that was treated with at least one induction course of BCG that progressed to MIBC. Outcomes analyzed included pathologic downstaging rates defined as <pT2/N0, pathologic complete response rates (pT0/N0), and survival outcomes (RFS, CSS, OS). Survival outcomes were analyzed using the Kaplan-Meier Method or Gray's test with log rank. Cox Proportional Hazards and semiparametric hazards models proposed by Fine and Gray were constructed to identify predictors of oncologic outcomes.
333 patients were included in the analysis (sMIBC: 48 vs pMIBC: 285). There were no differences in pathologic downstaging (sMIBC: 54% vs pMIBC: 51%, P = .67) or pathologic complete response (sMIBC: 33% vs pMIBC: 28, P = .46). Survival analysis showed no differences when patients were treated with NAC+RC in oncologic outcomes. On regression analysis, only >pT2 and N+ disease were predictors of poorer CSS and OS. Separate analysis of sMIBC patients whom underwent RC only (N = 61), demonstrated inferior oncologic outcomes to other cohorts (P < .01).
There were no differences in pathologic response or survival between pMIBC and sMIBC patients when managed with NAC and RC.
比较接受顺铂为基础的新辅助化疗(NAC)联合根治性膀胱切除术(RC)治疗的原发性肌层浸润性膀胱癌(pMIBC)和继发性肌层浸润性膀胱癌(sMIBC)患者的病理和生存结果。
我们回顾了 2010 年至 2019 年期间我院的 cT2-T4/N0 MIBC 患者。pMIBC 的定义为初始或重新分期 TURBT 时表现为>cT2 疾病,且无膀胱癌病史。sMIBC 的定义为既往接受过至少一次 BCG 诱导治疗的非肌层浸润性膀胱癌(NMIBC),进展为肌层浸润性膀胱癌。分析的结果包括病理降期率(定义为<pT2/N0)、病理完全缓解率(pT0/N0)和生存结果(RFS、CSS、OS)。使用 Kaplan-Meier 方法或 Gray 检验对数秩进行生存分析。构建 Cox 比例风险和 Fine 和 Gray 提出的半参数风险模型,以确定肿瘤学结果的预测因素。
共纳入 333 例患者进行分析(sMIBC:48 例,pMIBC:285 例)。两组患者在病理降期(sMIBC:54% vs pMIBC:51%,P=0.67)或病理完全缓解(sMIBC:33% vs pMIBC:28%,P=0.46)方面无差异。生存分析显示,接受 NAC+RC 治疗的患者在肿瘤学结果方面无差异。回归分析显示,仅>pT2 和 N+疾病是 CSS 和 OS 较差的预测因素。对仅接受 RC 治疗的 sMIBC 患者(N=61)进行单独分析,发现其肿瘤学结果较其他队列差(P<0.01)。
在接受 NAC 和 RC 治疗时,pMIBC 和 sMIBC 患者的病理反应和生存结果无差异。