Neoadjuvant Chemotherapy with Gemcitabine plus Cisplatin in Patients with Locally Advanced Bladder Cancer

被引:27
|
作者
Niedersuess-Beke, Dora [1 ]
Puntus, Thomas [2 ]
Kunit, Thomas [5 ]
Gruenberger, Birgit [4 ]
Lamche, Michael [3 ]
Loidl, Wolfgang [6 ]
Bohm, Reinhard [3 ]
Kraischits, Nicole [3 ]
Kudlacek, Stefan [2 ]
Schramek, Paul [3 ]
Meran, Johannes G. [2 ]
机构
[1] Wilhelminenspital Stadt Wien, Ctr Oncol Haematol & Palliat Care, Dept Med 1, Montleartstr 36, AT-1160 Vienna, Austria
[2] Barmherzige Bruder Krankenhaus Wien, Dept Med, Vienna, Austria
[3] Barmherzige Bruder Krankenhaus Wien, Dept Urol & Androl, Vienna, Austria
[4] Landesklinikum Wiener Neustadt, Dept Oncol, Vienna, Austria
[5] Paracelsus Private Med Univ Salzburg, Dept Urol & Androl, Salzburg, Austria
[6] Ordensklinikum Linz Barmherzige Schwestern, Dept Urol, Linz, Austria
关键词
Bladder cancer; Neoadjuvant chemotherapy; Cisplatin and gemcitabine; INVASIVE UROTHELIAL CARCINOMA; METHOTREXATE; VINBLASTINE; DOXORUBICIN; MULTICENTER; GUIDELINES; CYSTECTOMY;
D O I
10.1159/000463389
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Neoadjuvant chemotherapy with methotrexate-vinblastine-doxorubicin-cisplatin (MVAC) is the standard of care for muscle-invasive urothelial bladder cancer. Gemcitabine plus cisplatin (GC) shows similar efficacy with less toxicity in the metastatic setting and has therefore often been used interchangeably with MVAC. We report on the efficacy and safety of neoadjuvant GC in patients with locally advanced urothelial cancer. Materials and Methods: We prospectively evaluated 87 patients in 2 centers. Their median age was 68 years. Treatment consisted of 3x GC prior to radical cystectomy. The primary endpoint was pathologic response. The secondary endpoints were safety, progression-free survival (PFS), and overall survival (OS). Results: In all, 83 patients finished chemotherapy; 80 patients were evaluable for the primary endpoint. Pathologic complete response (pCR) was achieved in 22.5% and near pCR was seen in 33.7% of the patients. The 1-year PFS rate was 79.5% among those achieving pCR or near pCR (p = 0.041). Five-year OS was 61.8% (95% CI 67.6 to NA). GC was well tolerated. Grade 3/4 toxicities occurred in 38% of the patients. There was no grade 3/4 renal toxicity, febrile neutropenia, or death. Conclusion: Neoadjuvant GC is a well-tolerated regimen. Although the pathologic response is lower than that reported with MVAC, our data support GC as a feasible option in the absence of a prospective randomized comparison, particularly for older patients, since its toxicity is lower than that of MVAC. (C) 2017 S. Karger AG, Basel
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收藏
页码:36 / 42
页数:7
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