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Gemcitabine Single Agent for Recurrent Post Bladder Preservation Therapy and in Metastatic Transitional Cell Carcinoma of Urinary Bladder in Elderly Patients with Renal Impairment

机译:吉西他滨单药用于老年肾功能不全患者的复发性膀胱术后保存和膀胱转移性移行细胞癌的治疗

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Purpose : The objectives of the study are to evaluate efficacy (ORR, PFS, & OS) and toxicity of single-agent gemcitabine in recurrent post conservative therapy and in the metastatic transitional cell carcinoma of the urinary bladder in elderly patients with a renal impairment. Patients and Methods: Between March 2014 and September 2016 , Fourteen patients have recurrent post conservative therapy & in metastatic transitional cell cancer of the urinary bladder in elderly patients with renal impairment were included to receive single-agent gemcitabine (1,000 mg/m~(2)) administered weekly times three on a 4-week cycle. The median age was 74.5 years. The majority of patients (57.2%) have metastatic disease at diagnosis also a majority of patients (57.2%) have a solitary metastatic disease. The median overall treatment period was 14 weeks (range: 4-24 weeks). Results: Overall response rate was 35.7% (CR 7.1% + PR 28.6%). Median-Progression Free Survival was 20 weeks (95% CI: 95% CI: 8.313- 31.687). Median Overall survival rates were 40 weeks (95% CI: 28.313-51.687). 50% of patients experienced at least one grade 1 or 2 neutropenia and 71.5% of patients developed thrombocytopenia and no patient (0%) required hospitalization during therapy for neutropenic fever or dehydration . 50% patients required treatment delayed at least one week due to treatment toxicity. Conclusion: The single agent Gemcitabine had significant improvement in response rate, progression-free survival and overall survival with good tolerance and manageable toxicity.
机译:目的:该研究的目的是评估保守治疗后的复发和老年肾功能不全患者膀胱转移性移行细胞癌中吉西他滨单药的疗效(ORR,PFS和OS)和毒性。患者与方法:2014年3月至2016年9月,保守治疗后复发的14例患者和患有肾功能不全的老年膀胱转移性移行细胞癌患者均接受吉西他滨单药(1,000 mg / m〜(2 ))每周3次,每4周一次。中位年龄是74.5岁。大多数患者(57.2%)在诊断时患有转移性疾病,大多数患者(57.2%)患有孤立性转移性疾病。中位总体治疗期为14周(范围:4-24周)。结果:总体回应率为35.7%(CR 7.1%+ PR 28.6%)。中位数无进展生存期为20周(95%CI:95%CI:8.313-31.687)。中位总生存率为40周(95%CI:28.313-51.687)。 50%的患者至少经历过1级或2级中性粒细胞减少症,而71.5%的患者出现血小板减少症,在中性粒细胞减少或发热的治疗过程中无需住院(0%)。由于治疗毒性,需要治疗的患者中有50%至少延迟了一周。结论:吉西他滨单药具有显着改善的缓解率,无进展生存期和总生存期,耐受性好,毒性可控。

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