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Protracted low dose of oral vinorelbine and temozolomide with whole-brain radiotherapy in the treatment for breast cancer patients with brain metastases

机译:长期低剂量口服长春瑞滨和替莫唑胺全脑放疗治疗乳腺癌脑转移患者

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Purpose The management of brain metastases (BM) from breast cancer (BC) needs to be improved, and new therapeutic strategies are urgently requested. In this view, we have evaluated the efficacy, tolerability, and safety of concurrent low protracted dose of temozolomide (TMZ), metronomic oral vinorelbine (VNB), and radiotherapy in BC women with previously untreated BM. Methods Thirty-six patients with newly diagnosed BM were treated with TMZ orally administered at a dose of 75 mg/m 2 during whole-brain radiotherapy, followed by 4 weeks off-therapy and a subsequent administration of oral 70 mg/m 2 VNB fractionated in days 1, 3, and 5, weekly for three consecutive weeks plus TMZ at 75 mg/m 2 on days 1-21, all every 4 weeks for up to 12 additional cycles. The primary end point was the evaluation of the objective response rate (ORR). Results Three complete responses and 16 partial responses have been achieved with an ORR of 52 % (95 % CI 38-67 %) that exceeded the target activity per study design. The median progression-free survival and overall survival were 8 and 11 months, respectively. The schedule appeared to be well tolerated, and side effects were generally mild. The functional assessment of cancer therapybreast (FACT-B) analysis showed a significant positive change during the study. Conclusions In conclusion, the treatment was safe and a significant number of objective responses were observed with a significant improvement in quality of life demonstrated by FACT-B. On the basis of the present results, a large randomized trial is warranted in BC patients with previously untreated BM.
机译:目的需要改善乳腺癌(BC)引起的脑转移瘤(BM)的管理,迫切需要新的治疗策略。根据这种观点,我们评估了替莫唑胺(TMZ),节律性口服长春瑞滨(VNB)和放疗的同时低长期剂量替莫唑胺(BCZ)先前未经治疗的BM妇女的疗效,耐受性和安全性。方法对36例新诊断为BM的患者在全脑放疗期间口服TMZ口服,剂量为75 mg / m 2,停药4周,随后口服70 mg / m 2的VNB分级在第1、3和5天,连续三周每周一次,以及在1-21天以75 mg / m 2的TMZ剂量,每4周一次,最多连续12个周期。主要终点是客观反应率(ORR)的评估。结果根据研究设计,ORR达到52%(95%CI 38-67%)的情况下,已经完成了三个完全缓解和16个部分缓解。中位无进展生存期和总生存期分别为8个月和11个月。时间表似乎耐受良好,且副作用一般较轻。乳腺癌治疗功能评估(FACT-B)在研究期间显示出显着的积极变化。结论总之,该治疗是安全的,并且观察到大量客观反应,FACT-B证实生活质量显着改善。根据目前的结果,必须对先前未接受过BM治疗的BC患者进行大型随机试验。

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