Department of Medical Oncology, Hôpital Saint André, Bordeaux, France.
Oncology. 2011;80(3-4):214-8. doi: 10.1159/000329078. Epub 2011 Jul 1.
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 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.
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).
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.
背景/目的:当肿瘤表现出肉瘤样或 Fuhrman 分级 4 特征时,转移性肾细胞癌(mRCC)可能会迅速进展。已经报道了吉西他滨(Gem)联合多柔比星(Dox)在肉瘤样或快速进展性 mRCC 中的疗效。我们回顾性评估了 Gem + Dox 在这一特定患者人群中的连续队列中的疗效。
患者的东部合作肿瘤学组表现状态为 2 级或更高级别,且患有快速进展性 mRCC 或具有肉瘤样特征的 mRCC。Gem(1500mg/m²)和 Dox(50mg/m²)每 2 周给予一次,并给予粒细胞集落刺激因子。
29 名患者接受了治疗。6 名患者的肉瘤样特征占主导地位,而 14 名患者的肿瘤为 Fuhrman 分级 4。所有患者在 4 个月内均出现进展性 mRCC。未报告 4 级毒性或与药物相关的死亡。观察到 1 例部分缓解(7 个月)、1 例混合反应和 14 例稳定疾病(9 例患者≥4 个月),而肉瘤样肿瘤未见反应。无疾病进展生存期的中位数为 3.7 个月(8 例患者≥6 个月),总生存期的中位数为 4.8 个月(5 例患者>12 个月)。
本研究的缓解率低于先前报道的结果。然而,一些患者的生存时间延长。该联合方案可用于肉瘤样组织学(NCCN 指南)或快速进展性疾病,但该人群代表了未满足的医疗需求。