Yoneyama Takahiro, Tobisawa Yuki, Yoneyama Tohru, Yamamoto Hayato, Imai Atsushi, Hatakeyama Shingo, Hashimoto Yasuhiro, Koie Takuya, Ohyama Chikara
Department of Urology, Hirosaki University Graduate School of Medicine, 5 Zaifucho, Hirosaki, Aomori, 036-8562, Japan.
Int J Clin Oncol. 2015 Apr;20(2):369-74. doi: 10.1007/s10147-014-0706-2. Epub 2014 May 29.
We evaluated retrospectively the feasibility and effectiveness of carboplatin-based combination chemotherapy in elderly patients with advanced bladder cancer.
Forty-seven patients with advanced bladder cancer (33 men and 14 women) and treated at our hospital between August 2004 and December 2011 were enrolled. The average age was 77.1 years (range 70-86 years), the average creatinine clearance was 37.0 ml/min (range 14.5-113.0 ml/min), and the average follow-up period was 17.4 months (range 10-55 months). Twenty-nine patients (61.7 %) were unfit for cisplatin-based chemotherapy. There were 15 recurrent cases after radical surgery and 32 inoperable cases. In this study, the first-line therapy was gemcitabine and carboplatin (GCarbo), with two courses as a set. The second-line therapy was GCarbo and docetaxel (GCarboD) if there was an insufficient response to the first-line therapy.
Of the 47 patients who underwent GCarbo therapy, the response rate was 38.3 % (complete response plus partial response), with 5 and 13 patients exhibiting a complete response and a partial response, respectively. The average response duration was 15.7 months (range 2-42 months). The response rate of the nine patients who received GCarboD was 11.1 %, and the overall median survival was 15.0 months. Adverse events occurred in 30 patients (63.8 %) who underwent GCarbo therapy. Bone marrow suppression was observed in 30 patients (61.7 %), and digestive symptoms were observed in three patients (9.0 %).
Our study demonstrates that GCarbo is a safe and effective combination chemotherapy in elderly patients with advanced bladder cancer. However, the GCarboD regimen appears to have limited effectiveness for nonresponders to GCarbo therapy.
我们回顾性评估了以卡铂为基础的联合化疗在老年晚期膀胱癌患者中的可行性和有效性。
纳入2004年8月至2011年12月在我院接受治疗的47例晚期膀胱癌患者(33例男性和14例女性)。平均年龄为77.1岁(范围70 - 86岁),平均肌酐清除率为37.0 ml/min(范围14.5 - 113.0 ml/min),平均随访期为17.4个月(范围10 - 55个月)。29例患者(61.7%)不适合基于顺铂的化疗。有15例根治性手术后复发病例和32例不可手术病例。在本研究中,一线治疗为吉西他滨和卡铂(GCarbo),以两个疗程为一组。如果对一线治疗反应不足,二线治疗为GCarbo和多西他赛(GCarboD)。
在接受GCarbo治疗的47例患者中,缓解率为38.3%(完全缓解加部分缓解),分别有5例和13例患者表现出完全缓解和部分缓解。平均缓解持续时间为15.7个月(范围2 - 42个月)。接受GCarboD治疗的9例患者的缓解率为11.1%,总体中位生存期为15.0个月。30例接受GCarbo治疗的患者发生了不良事件(63.8%)。30例患者(61.7%)观察到骨髓抑制,3例患者(9.0%)观察到消化系统症状。
我们的研究表明,GCarbo对老年晚期膀胱癌患者是一种安全有效的联合化疗。然而,GCarboD方案对GCarbo治疗无反应者的有效性似乎有限。