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多西他赛每周给药作为转移性尿路上皮癌患者二线化疗的II期研究

A Phase II Study of Weekly Docetaxel as Second-Line Chemotherapy in Patients With Metastatic Urothelial Carcinoma.

作者信息

Kim Young Saing, Lee Soon Il, Park Se Hoon, Park Silvia, Hwang In Gyu, Lee Sang-Cheol, Sun Jong-Mu, Lee Jeeyun, Lim Ho Yeong

机构信息

Division of Hematology and Oncology, Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Republic of Korea.

Division of Hematology-Oncology, Department of Medicine, Dankook University Hospital, Dankook University College of Medicine, Cheonan, Republic of Korea.

出版信息

Clin Genitourin Cancer. 2016 Feb;14(1):76-81. doi: 10.1016/j.clgc.2015.09.008. Epub 2015 Sep 25.

Abstract

UNLABELLED

The present multicenter phase II study evaluated the efficacy and safety of weekly docetaxel as second-line chemotherapy for metastatic urothelial carcinoma. Weekly docetaxel was well tolerated but demonstrated modest activity, with a response rate of 6%, a median progression-free survival (PFS) of 1.4 months, and a median overall survival (OS) of 8.3 months. The dichotomy between PFS and OS was likely associated with subsequent platinum-based chemotherapy received by 58% of the patients.

BACKGROUND

Docetaxel is commonly used for second-line therapy for metastatic urothelial carcinoma (UC). However, myelosuppression is a substantial concern when the traditional 3-week docetaxel cycle is used. The present multicenter phase II study evaluated the efficacy and safety of weekly docetaxel as second-line chemotherapy for metastatic UC.

PATIENTS AND METHODS

Patients with progression after previous platinum-based chemotherapy for advanced or metastatic disease were treated with docetaxel 30 mg/m(2) on days 1 and 8 every 21 days. The primary endpoint was the response rate.

RESULTS

The study enrolled 31 patients. Their median age was 64 years (range, 40-79 years). An Eastern Cooperative Oncology Group performance status of 1, liver metastasis, and a hemoglobin level < 10 g/dL were observed in 100%, 32%, and 23% of patients, respectively. Previous platinum-based chemotherapy had been administered for metastatic disease in 29 patients (94%). Although fatigue (13%) and anorexia (6%) were the most frequently observed grade 3 to 4 toxicities, the safety profiles were generally mild and manageable. Two patients (6%) achieved an objective response, which was maintained for 3.0 to 7.8 months. Eight patients experienced disease stabilization (disease control rate, 32%). The median progression-free survival (PFS) and overall survival (OS) were 1.4 months (95% confidence interval [CI], 1.3-1.6) and 8.3 months (95% CI, 5.9-10.6), respectively. A relatively long OS was associated with further salvage platinum-based chemotherapy (n = 18, 58%) showing an encouraging activity (response rate, 44%; median PFS, 4.0 months).

CONCLUSION

Second-line chemotherapy with weekly docetaxel was well tolerated but demonstrated modest activity in patients with metastatic UC. A platinum-based combination as second-line treatment might be considered for selected patients.

摘要

未标注

本多中心II期研究评估了每周一次多西他赛作为转移性尿路上皮癌二线化疗的疗效和安全性。每周一次多西他赛耐受性良好,但活性一般,缓解率为6%,中位无进展生存期(PFS)为1.4个月,中位总生存期(OS)为8.3个月。PFS和OS之间的差异可能与58%的患者随后接受铂类化疗有关。

背景

多西他赛常用于转移性尿路上皮癌(UC)的二线治疗。然而,使用传统的每3周一次多西他赛周期时,骨髓抑制是一个重大问题。本多中心II期研究评估了每周一次多西他赛作为转移性UC二线化疗的疗效和安全性。

患者和方法

先前接受铂类化疗后出现晚期或转移性疾病进展的患者,每21天在第1天和第8天接受30mg/m²多西他赛治疗。主要终点是缓解率。

结果

该研究纳入了31例患者。他们的中位年龄为64岁(范围40 - 79岁)。分别有100%、32%和23%的患者东部肿瘤协作组体能状态评分为1、有肝转移且血红蛋白水平<10g/dL。29例(94%)患者先前接受过铂类化疗用于转移性疾病。尽管疲劳(13%)和厌食(6%)是最常观察到的3 - 4级毒性,但安全性总体较轻且可控。2例患者(6%)达到客观缓解,缓解持续3.0至7.8个月。8例患者病情稳定(疾病控制率32%)。中位无进展生存期(PFS)和总生存期(OS)分别为1.4个月(95%置信区间[CI],1.3 - 1.6)和8.3个月(95%CI,5.9 - 10.6)。相对较长的OS与进一步的挽救性铂类化疗(n = 18,58%)有关,后者显示出令人鼓舞的活性(缓解率44%;中位PFS,4.0个月)。

结论

每周一次多西他赛二线化疗耐受性良好,但在转移性UC患者中活性一般。对于部分患者,可考虑铂类联合方案作为二线治疗。

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