Kwinta Łukasz, Konopka Kamil, Okoń Krzysztof, Łobacz Mateusz, Chłosta Piotr, Dudek Przemysław, Buda-Nowak Anna, Potocki Paweł, Wysocki Piotr J
Oncology Department, Faculty of Medicine, Jagiellonian University Medical College, 31-501 Krakow, Poland.
Clinical Department of Oncology, University Hospital in Krakow, 31-501 Kraków, Poland.
Cancers (Basel). 2025 Jan 14;17(2):258. doi: 10.3390/cancers17020258.
: Bladder cancer is a significant clinical problem with approximately 500,000 new cases worldwide annually. In approximately 25% of cases, disease is diagnosed at a stage of invasion of the muscle layer of the bladder. The current standard approach in this disease is preoperative chemotherapy followed by radical cystectomy. Dose-dense MVAC (ddMVAC), a two-day chemotherapy regimen, is the reference treatment protocol in this setting. The presented study evaluated the effectiveness and safety of accelerated MVAC (aMVAC) chemotherapy-a one-day regimen given before the resection of the bladder due to muscle-invasive disease. : A retrospective analysis included 119 consecutive patients diagnosed with urothelial muscle-invasive bladder cancer (MIBC) who underwent preoperative chemotherapy with the aMVAC regimen. The planned treatment included 4-6 cycles of preoperative chemotherapy. The analysis of the degree of histopathological response to treatment was based on the three-grade TRG (tumor regression grade) classification. : A complete pathological response (TRG1) was observed in 44 patients (36.7%), and a major pathologic response (<ypT2) was achieved in 58 patients (48.7%). A reduction in the cisplatin dose was associated with a statistically significant decrease in the chance of achieving complete pathologic responses (46.1% vs. 10%, RR for TRG1 = 0.69, = 0.00118). Patients who received at least 4 cycles (compared to ≤3 cycles) of neoadjuvant chemotherapy had a significantly higher chance of achieving a pathological response (partial or complete) to treatment (78.1% vs. 52.2%, RR 0.68, = 0.0374). Administration of at least five cycles of chemotherapy was associated (compared to four cycles) with a significantly higher likelihood of achieving a complete pathological response (63.2% vs. 33.8%, RR = 1.71, = 0.0221). The vast majority of adverse events were in grades 1 and 2, according to CTCAE version 5.0. Only five patients experienced grade 3-4 toxicities. The most common adverse event was anemia, which occurred in 66.3% of patients. : Our real-world data analysis confirms the activity, safety, and feasibility of the aMVAC regimen as neoadjuvant chemotherapy in patients with urothelial MIBC.
膀胱癌是一个重大的临床问题,全球每年约有50万新发病例。在大约25%的病例中,疾病在膀胱肌层浸润阶段被诊断出来。这种疾病目前的标准治疗方法是术前化疗,然后进行根治性膀胱切除术。剂量密集型MVAC(ddMVAC),一种为期两天的化疗方案,是这种情况下的参考治疗方案。本研究评估了加速MVAC(aMVAC)化疗的有效性和安全性,这是一种在因肌肉浸润性疾病而进行膀胱切除术前给予的为期一天的方案。
一项回顾性分析纳入了119例连续诊断为尿路上皮肌肉浸润性膀胱癌(MIBC)并接受aMVAC方案术前化疗的患者。计划的治疗包括4 - 6个周期的术前化疗。对治疗的组织病理学反应程度的分析基于三级TRG(肿瘤消退分级)分类。
44例患者(36.7%)观察到完全病理缓解(TRG1),58例患者(48.7%)实现了主要病理缓解(<ypT2)。顺铂剂量的减少与实现完全病理缓解的机会在统计学上显著降低相关(46.1%对10%,TRG1的RR = 0.69, = 0.00118)。接受至少4个周期(与≤3个周期相比)新辅助化疗的患者对治疗产生病理反应(部分或完全)的机会显著更高(78.1%对52.2%,RR 0.68, = 0.0374)。与4个周期相比,给予至少5个周期的化疗与实现完全病理缓解的可能性显著更高相关(63.2%对33.8%,RR = 1.71, = 0.0221)。根据CTCAE第5.0版,绝大多数不良事件为1级和2级。只有5例患者经历了3 - 4级毒性反应。最常见的不良事件是贫血,发生在66.3%的患者中。
我们的真实世界数据分析证实了aMVAC方案作为尿路上皮MIBC患者新辅助化疗的活性、安全性和可行性。