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在先前接受基于顺铂的围手术期治疗后,基于顺铂的一线治疗用于晚期尿路上皮癌。

Cisplatin-based first-line therapy for advanced urothelial carcinoma after previous perioperative cisplatin-based therapy.

作者信息

Necchi Andrea, Pond Gregory R, Giannatempo Patrizia, Di Lorenzo Giuseppe, Eigl Bernhard J, Locke Jenn, Pal Sumanta K, Agarwal Neeraj, Poole Austin, Vaishampayan Ulka N, Niegisch Guenter, Hussain Syed A, Singh Parminder, Bellmunt Joaquim, Sonpavde Guru

机构信息

Department of Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Department of Statistics, McMaster University, Hamilton, Ontario, Canada.

出版信息

Clin Genitourin Cancer. 2015 Apr;13(2):178-84. doi: 10.1016/j.clgc.2014.08.010. Epub 2014 Sep 23.

Abstract

BACKGROUND

Outcomes with cisplatin-based first-line therapy for advanced UC after previous perioperative cisplatin-based chemotherapy are unclear. In this study we evaluated outcomes with a focus on the effect of time from previous cisplatin-based perioperative chemotherapy.

PATIENTS AND METHODS

Data were collected for patients who received cisplatin-based first-line therapy for advanced UC after previous perioperative cisplatin-based therapy. Cox proportional hazards models were used to investigate the prognostic ability of visceral metastasis, ECOG PS, TFPC, anemia, leukocytosis, and albumin on overall survival (OS).

RESULTS

Data were available for 41 patients from 8 institutions including 31 men (75.6%). The median age was 61 (range, 41-77) years, most received gemcitabine plus cisplatin (n = 26; 63.4%), and the median number of cycles was 4 (range, 1-8). The median OS was 68 weeks (95% confidence interval [CI], 48.0-81.0). Multivariable Cox regression analysis results showed an independent prognostic effect on OS for PS > 0 versus 0 (hazard ratio [HR], 4.56 [95% CI, 1.66-12.52]; P = .003) and TFPC ≥ 78 weeks versus < 78 weeks (HR, 0.48 [95% CI, 0.21-1.07]; P = .072). The prognostic model for OS was internally validated with c-index = 0.68. Patients with TFPC < 52 weeks, 52 to 104 weeks, and ≥ 104 weeks had median survival of 42, 70, and 162 weeks, respectively.

CONCLUSION

Longer TFPC ≥ 78 weeks and ECOG PS = 0 were independently prognostic for better survival with cisplatin-based first-line chemotherapy for advanced UC after previous perioperative cisplatin-based chemotherapy. The data support using TFPC ≥ 52 weeks to rechallenge with cisplatin-based first-line chemotherapy for metastatic disease.

摘要

背景

对于既往接受过基于顺铂的围手术期化疗后的晚期尿路上皮癌(UC)患者,采用基于顺铂的一线治疗的疗效尚不清楚。在本研究中,我们评估了疗效,并重点关注距既往基于顺铂的围手术期化疗的时间的影响。

患者与方法

收集了既往接受过基于顺铂的围手术期化疗后接受基于顺铂的一线治疗的晚期UC患者的数据。采用Cox比例风险模型研究内脏转移、东部肿瘤协作组(ECOG)体能状态(PS)、距既往顺铂围手术期化疗的时间(TFPC)、贫血、白细胞增多和白蛋白对总生存期(OS)的预后能力。

结果

来自8家机构的41例患者的数据可用,其中男性31例(75.6%)。中位年龄为61岁(范围41 - 77岁),大多数患者接受吉西他滨联合顺铂治疗(n = 26;63.4%),中位周期数为4个周期(范围1 - 8个周期)。中位OS为68周(95%置信区间[CI],48.0 - 81.0)。多变量Cox回归分析结果显示,PS>0对比PS = 0对OS有独立的预后影响(风险比[HR],4.56[95%CI,1.66 - 12.52];P = 0.003),TFPC≥78周对比<78周(HR,0.48[95%CI,0.21 - 1.07];P = 0.072)。OS的预后模型经内部验证,c指数 = 0.68。TFPC<52周、52至104周和≥104周的患者中位生存期分别为42周、70周和162周。

结论

对于既往接受过基于顺铂的围手术期化疗后的晚期UC患者,基于顺铂的一线化疗中,较长的TFPC≥78周和ECOG PS = 0对更好的生存具有独立的预后意义。数据支持对于转移性疾病,使用TFPC≥52周再次接受基于顺铂的一线化疗。

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本文引用的文献

1
Patient eligibility and trial design for the salvage therapy of advanced urothelial carcinoma.
Clin Genitourin Cancer. 2014 Dec;12(6):395-8. doi: 10.1016/j.clgc.2014.03.016. Epub 2014 Jun 10.
3
Adjuvant chemotherapy for invasive bladder cancer: a 2013 updated systematic review and meta-analysis of randomized trials.
Eur Urol. 2014 Jul;66(1):42-54. doi: 10.1016/j.eururo.2013.08.033. Epub 2013 Aug 28.
5
A new approach to second-line therapy for urothelial cancer?
Lancet Oncol. 2013 Jul;14(8):682-4. doi: 10.1016/S1470-2045(13)70175-X. Epub 2013 May 22.
6
Prognostic model for predicting survival of patients with metastatic urothelial cancer treated with cisplatin-based chemotherapy.
J Natl Cancer Inst. 2013 Apr 3;105(7):499-503. doi: 10.1093/jnci/djt015. Epub 2013 Feb 14.
9
Accelerated MVAC chemotherapy in patients with advanced bladder cancer previously treated with a platinum-gemcitabine regimen.
Eur J Cancer. 2012 May;48(8):1141-6. doi: 10.1016/j.ejca.2012.01.022. Epub 2012 Feb 22.

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