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

机译:多中心II期研究,每周使用苯达莫司汀和紫杉醇作为转移性乳腺癌患者的一线或后线治疗:RiTa II试验

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摘要

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 (Cl): 5.5-10.9) and 14.9 months (95% Cl: 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.
机译:在先前的RiTa I试验中已评估了苯达莫司汀(B)和紫杉醇(P)在晚期乳腺癌患者中作为无蒽环类药物的治疗选择的组合。建立每周B 70 mg / m〜2和P 90 mg / m〜2的方案,每4周暂停一次,是一种低毒的有效方案。本RiTa II研究的目的是研究BP作为无蒽环类联合疗法的潜力。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)。一共有26例患者,其中一线接受了15例血压,一线治疗后有11例接受了血压。 27%的患者患有三阴性乳腺癌(TNBC)。中位PFS和OS分别为7.3个月(95%置信区间(Cl):5.5-10.9)和14.9个月(95%Cl:9.9-22.9)。 1年PFS率为20.3%,1年OS率为71.2%。 ORR为42.3%,包括4个完全缓解和7个部分缓解。 TNBC患者的ORR达到71.4%。接受蒽环类药物治疗的患者的ORR为43.8%,证实苯达莫司汀对蒽环类药物缺乏交叉耐药性。 BP是治疗转移性乳腺癌的中毒性反应的理想选择,为蒽环类药物预处理和TNBC患者的应用提供了可能性。

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