Kuş Tülay, Aktaş Gökmen
Department of Medical Oncology, Gaziantep University School of Medicine, Gaziantep, Turkey.
Turk J Urol. 2017 Sep;43(3):273-278. doi: 10.5152/tud.2017.24478. Epub 2017 Jul 31.
To investigate the effects of gemcitabine maintenance treatment on survival in patients with metastatic bladder cancer.
Gemcitabine maintenance monotherapy was administered following the standard platinum-gemcitabine therapy in patients with metastatic bladder cancer. Patients who had responded to standard treatment received maintenance gemcitabine therapy as 1000 mg/m on days 1 and 8 every three weeks until progression or development of unacceptable toxicity. The following clinical factors were noted: performance status, age, sex, stage, site of metastasis, choice of cisplatin-gemcitabine or carboplatin-gemcitabine, response rates to the initial chemotherapy. Progression-free survival (PFS) and overall survival (OS) for standard treatment, and following gemcitabine monotreatment and for maintenance gemcitabine therapy were calculated using Kaplan-Meier method.
A total of 88 patients with metastatic bladder cancer treated between February 2009 to October 2015 were evaluated retrospectively and 23 patients (26.1%) who had responded to six cycles of platinum-gemcitabine treatment were included in this study. Maintenance gamcitabine was administered for a median of 7 times (range 3-14 times). Grade 3 hematotoxicity according to the criteria of the Common Terminology Criteria of Adverse Events was observed in 7 (30.4%) patients. Median PFS of patients was 46 (range: 30-82) weeks for platinum-based treatment plus maintenance gemcitabine therapy. A higher median PFS was obtained in patients who were <65 year-olds, without organ metastasis with objective response rate, however, it was statistically insignificant.
Gemcitabine maintenance therapy in metastatic bladder cancer patients who did not shown progression after the standard platinum-gemcitabine treatment contributes to survival and presents low toxicity profile, when compared to historical controls.
探讨吉西他滨维持治疗对转移性膀胱癌患者生存的影响。
在转移性膀胱癌患者中,标准铂类-吉西他滨治疗后给予吉西他滨维持单药治疗。对标准治疗有反应的患者接受维持吉西他滨治疗,剂量为1000mg/m²,每三周的第1天和第8天给药,直至病情进展或出现不可接受的毒性反应。记录以下临床因素:体能状态、年龄、性别、分期、转移部位、顺铂-吉西他滨或卡铂-吉西他滨的选择、初始化疗的缓解率。使用Kaplan-Meier方法计算标准治疗、吉西他滨单药治疗及维持吉西他滨治疗后的无进展生存期(PFS)和总生存期(OS)。
回顾性评估了2009年2月至2015年10月期间治疗的88例转移性膀胱癌患者,其中23例(26.1%)对六个周期的铂类-吉西他滨治疗有反应的患者纳入本研究。维持吉西他滨治疗的中位次数为7次(范围3 - 14次)。根据不良事件通用术语标准,7例(30.4%)患者出现3级血液学毒性。铂类治疗加维持吉西他滨治疗患者的中位PFS为46周(范围:30 - 82周)。年龄<65岁、无器官转移且有客观缓解率的患者获得了较高的中位PFS,但差异无统计学意义。
与历史对照相比,标准铂类-吉西他滨治疗后未出现进展的转移性膀胱癌患者接受吉西他滨维持治疗有助于生存,且毒性较低。