Multicenter Phase II Study with Weekly Bendamustine and Paclitaxel as First- or Later-Line Therapy in Patients with Metastatic Breast Cancer: RiTa II Trial.

Breast care (Basel, Switzerland) Pub Date : 2011-12-01 Epub Date: 2011-12-15 DOI:10.1159/000335199
Sibylle Loibl, Gabriele Doering, Lothar Müller, Albert Grote-Metke, Roberto Müller, Oliver Tomé, Wolfgang Wiest, Andrea Maisch, Valentina Nekljudova, Gunter von Minckwitz
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引用次数: 1

Abstract

The combination of bendamustine (B) and paclitaxel (P) as anthracycline-free treatment option in patients with advanced breast cancer has been evaluated in the previous RiTa I trial. The regimen of weekly B 70 mg/m(2) and P 90 mg/m(2) with a pause every 4th week was established as an effective regimen with low toxicity. The aim of the present RiTa II study was to investigate the potential of BP as anthracycline-free combination therapy. The primary objective was to determine the progression-free survival (PFS); secondary endpoints were safety, tolerability, overall response rate (ORR) and overall survival (OS). 26 patients were available, 15 received BP as first-line, 11 as beyond first-line treatment. 27% patients had triple-negative breast cancer (TNBC). Median PFS and OS were 7.3 months (95% confidence interval (CI): 5.5-10.9) and 14.9 months (95% CI: 9.9-22.9), respectively. The 1-year PFS rate was 20.3% and the 1-year OS rate 71.2%. The ORR was 42.3%, including 4 complete and 7 partial remissions. TNBC patients reached an ORR of 71.4%. Anthracycline-pretreated patients showed an ORR of 43.8%, confirming bendamustine's lack of cross-resistance to anthracycline agents. BP represents a favorable option with moderate toxicity in pretreated metastatic breast cancer and offers a possibility for application in anthracycline-pretreated and TNBC patients.

每周一次苯达莫司汀和紫杉醇作为转移性乳腺癌患者一线或后期治疗的多中心II期研究:RiTa II试验。
苯达莫司汀(B)联合紫杉醇(P)作为无蒽环类药物治疗晚期乳腺癌患者的选择已经在之前的RiTa I试验中进行了评估。每周给予B 70 mg/m(2)和P 90 mg/m(2),每4周暂停一次,是一种低毒性的有效方案。目前RiTa II研究的目的是探讨BP作为无蒽环类药物联合治疗的潜力。主要目的是确定无进展生存期(PFS);次要终点是安全性、耐受性、总缓解率(ORR)和总生存期(OS)。26例患者,15例接受一线BP治疗,11例接受超一线治疗。27%的患者为三阴性乳腺癌(TNBC)。中位PFS和OS分别为7.3个月(95%可信区间(CI): 5.5-10.9)和14.9个月(95% CI: 9.9-22.9)。1年PFS为20.3%,1年OS为71.2%。ORR为42.3%,其中完全缓解4例,部分缓解7例。TNBC患者的ORR达到71.4%。蒽环类药物预处理患者的ORR为43.8%,证实苯达莫司汀对蒽环类药物缺乏交叉耐药。BP是治疗前转移性乳腺癌的一种有利选择,毒性适中,并为蒽环类药物治疗前和TNBC患者提供了应用的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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