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首页> 外文期刊>Urologic oncology >Neoadjuvant chemotherapy with gemcitabine/cisplatin vs. methotrexate/vinblastine/doxorubicin/cisplatin for muscle-invasive urothelial carcinoma of the bladder: A retrospective analysis from the University of Southern California
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Neoadjuvant chemotherapy with gemcitabine/cisplatin vs. methotrexate/vinblastine/doxorubicin/cisplatin for muscle-invasive urothelial carcinoma of the bladder: A retrospective analysis from the University of Southern California

机译:吉西他滨/顺铂与甲氨蝶呤/长春碱/阿霉素/顺铂的新辅助化学疗法治疗肌肉侵袭性膀胱尿路上皮癌:南加州大学的回顾性分析

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Objectives: We evaluated pathologic and survival outcomes of GC (gemcitabine/cisplatin) and methotrexate/vinblastine/doxorubicin/cisplatin (M-VAC) neoadjuvant chemotherapy (NAC) in patients with muscle-invasive bladder cancer (MIBC). Materials and methods: A retrospective analysis of prospectively collected data on 116 patients who received NAC (GC: n = 58; M-VAC: n = 58) before radical cystectomy and superextended pelvic lymph node dissection for clinical stage T2-4N0M0 bladder cancer was performed. The outcomes were complete response rate (CRR; pT0N0), partial response rate (PRR; pT0N0, pTaN0, pT1N0, or pTisN0), overall mortality (OM), and recurrence. The Kaplan-Meier method and multivariable Cox regression analysis were used to analyze OM. The cumulative incidence method and Fine and Gray's competing risk regression analysis were used to analyze recurrence. Results: The median follow-up duration was 2.1 years for the GC group and 7.4 years for the M-VAC group (P < 0.001). There were no statistically significant differences between the GC and M-VAC groups with regard to CRR (27.3% vs. 17.1%, P = 0.419) or PRR (45.5% vs. 37.1%, P = 0.498). The predicted 5-year freedom from OM rate (P = 0.634) and cumulative incidence of recurrence rate (P = 0.891) did not differ between the GC and M-VAC groups. Multivariable analysis showed that there was no independent association between type of NAC and OM (P = 0.721) or recurrence (P = 0.065). Conclusions: Pathologic and survival outcomes did not differ in patients who received GC and M-VAC NAC. These data support the use of the GC regimen in the neoadjuvant setting.
机译:目的:我们评估了肌浸润性膀胱癌(MIBC)患者中GC(吉西他滨/顺铂)和甲氨蝶呤/长春碱/阿霉素/顺铂(M-VAC)新辅助化疗(NAC)的病理和生存结果。材料和方法:回顾性分析了116例行T2-4N0M0期膀胱癌根治性膀胱切除术和超长盆腔淋巴结清扫术前接受NAC(GC:n = 58; M-VAC:n = 58)的患者的前瞻性分析。执行。结果是完全缓解率(CRR; pT0N0),部分缓解率(PRR; pT0N0,pTaN0,pT1N0或pTisN0),总死亡率(OM)和复发。使用Kaplan-Meier方法和多变量Cox回归分析来分析OM。使用累积发生率方法和Fine和Gray的竞争风险回归分析来分析复发。结果:GC组中位随访时间为2.1年,M-VAC组中位随访时间为7.4年(P <0.001)。 GC组和M-VAC组之间在CRR(27.3%vs. 17.1%,P = 0.419)或PRR(45.5%vs. 37.1%,P = 0.498)方面无统计学差异。 GC和M-VAC组之间,预计的5年不受OM率影响(P = 0.634)和累积复发率(P = 0.891)没有差异。多变量分析显示,NAC类型与OM(P = 0.721)或复发(P = 0.065)之间没有独立的关联。结论:接受GC和M-VAC NAC的患者的病理学和生存结局无差异。这些数据支持在新辅助治疗中使用GC方案。

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