Department of Urology, University of California San Francisco, San Francisco, CA 94143, USA.
Urol Oncol. 2010 Sep-Oct;28(5):510-4. doi: 10.1016/j.urolonc.2008.11.019. Epub 2009 Jan 26.
Currently, there are few options other than cystectomy for the management of BCG refractory non-muscle invasive bladder cancer. We report our experience with intravesical combination chemotherapy using gemcitabine and MMC in such patients.
We identified all patients with non-muscle invasive bladder cancer who were BCG refractory or intolerant and had been treated with intravesical gemcitabine and MMC at our institution. Patients were treated with a combination of intravesical gemcitabine (1000 mg in 50 ml sterile water) followed sequentially by intravesical MMC (40 mg in 20 ml sterile water) every week for 6 weeks (induction). Induction therapy was followed by a maintenance regimen using the same dose of gemcitabine and MMC once a month for 12 months. Data regarding patient demographics and disease information such as previous intravesical therapy, previous cystoscopy, cytology results, time to recurrence, and side effect profile were collected.
A total of 10 patients (6 male and 4 female) aged 48 to 85 years (median 67 years) underwent treatment with a median follow-up of 26.5 months (4-34 months). Six patients were recurrence free and have maintained their response at a median of 14 months (4-34 months). Four patients had biopsy proven recurrence. Median time to recurrence was 6 months (range 4-13 months). The therapy was well tolerated in all patients. There were no major complications. Two patients experienced irritative lower urinary tract symptoms, which did not require cessation of therapy and one experienced a maculopapillary rash that improved with benadryl.
In patients with recurrent BCG refractory bladder cancer, intravesical combination chemotherapy with gemcitabine and MMC appears to be well tolerated and yields a response in a good proportion number of patients.
目前,除了膀胱切除术之外,对于卡介苗难治性非肌肉浸润性膀胱癌患者,几乎没有其他选择。我们报告了在这些患者中使用吉西他滨和丝裂霉素 C 进行膀胱内联合化疗的经验。
我们确定了所有在我们机构接受过卡介苗难治性或不耐受性非肌肉浸润性膀胱癌治疗且接受过膀胱内吉西他滨和丝裂霉素 C 治疗的患者。患者每周接受一次膀胱内吉西他滨(1000mg 溶于 50ml 无菌水中)联合丝裂霉素 C(40mg 溶于 20ml 无菌水中),共 6 周(诱导期)。诱导治疗后,采用相同剂量的吉西他滨和丝裂霉素 C 每月 1 次进行维持治疗 12 个月。收集患者的人口统计学和疾病信息,如既往膀胱内治疗、既往膀胱镜检查、细胞学结果、复发时间和副作用情况。
共有 10 名患者(6 名男性和 4 名女性),年龄 48 至 85 岁(中位年龄 67 岁),中位随访时间为 26.5 个月(4-34 个月)。6 名患者无复发,中位缓解时间为 14 个月(4-34 个月)。4 名患者活检证实复发。中位复发时间为 6 个月(范围 4-13 个月)。所有患者均能耐受该治疗,无严重并发症。2 名患者出现刺激性下尿路症状,但无需停止治疗,1 名患者出现斑丘疹皮疹,用苯海拉明后改善。
对于复发的卡介苗难治性膀胱癌患者,膀胱内联合化疗使用吉西他滨和丝裂霉素 C 似乎具有良好的耐受性,并能使相当比例的患者获得缓解。