Combination of Gemcitabine and Doxorubicin in Rapidly Progressive Metastatic Renal Cell Carcinoma and/or Sarcomatoid Renal Cell Carcinoma

被引:19
|
作者
Roubaud, G. [1 ]
Gross-Goupil, M. [1 ]
Wallerand, H. [2 ]
de Clermont, H. [3 ]
Dilhuydy, M. S. [1 ]
Ravaud, A. [1 ]
机构
[1] Bordeaux Univ Hosp, Dept Med Oncol, Hop St Andre, FR-33075 Bordeaux, France
[2] Bordeaux Univ Hosp, Grp Hosp Pellegrin, Dept Urol Androl & Renal Transplantat, FR-33075 Bordeaux, France
[3] Bordeaux Univ Hosp, Grp Hosp Pellegrin, Dept Nucl Med, FR-33075 Bordeaux, France
关键词
Metastatic renal cell carcinoma; Chemotherapy; Doxorubicin; Gemcitabine; National Comprehensive Cancer Network guidelines; PROGNOSTIC-FACTORS; PHASE-II; CHEMOTHERAPY; SURVIVAL; CANCER; RARE;
D O I
10.1159/000329078
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aims: Metastatic renal cell carcinoma (mRCC) can be rapidly progressive when tumors exhibit sarcomatoid or Fuhrman grade 4 features. Efficacy of gemcitabine (Gem) with doxorubicin (Dox) in sarcomatoid or rapidly progressive mRCC has been reported. We retrospectively evaluated Gem + Dox in a consecutive cohort of this particular patient population. Patients and Methods: Patients had an Eastern Cooperative Oncology Group performance status of 2 or more and rapidly progressive mRCC or mRCC with sarcomatoid features. Gem (1,500 mg/m(2)) and Dox (50 mg/m(2)) were given every 2 weeks with granulocyte colony-stimulating factor. Results: Twenty-nine patients were treated. Sarcomatoid features were predominant in 6 patients, while 14 tumors were Fuhrman grade 4. All patients had progressive mRCC within 4 months. No grade 4 toxicity or drug-related death was reported. One partial response (7 months), 1 mixed response, and 14 stable diseases (>= 4 months for 9 patients) were observed and no response was seen in sarcomatoid tumors. The median disease-free survival was 3.7 months (>= 6 months for 8 patients) and the median overall survival was 4.8 months (>12 months for 5 patients). Conclusion : This study showed a lower response rate than previously reported. Nevertheless, some patients had prolonged survival outcomes. This combination could be an option in sarcomatoid histology (NCCN guidelines) or rapidly progressive disease, but this population represents an unmet medical need. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:214 / 218
页数:5
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