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首页> 外文期刊>Breast Cancer Research >Safety and efficacy of vinorelbine in combination with pertuzumab and trastuzumab for first-line treatment of patients with HER2-positive locally advanced or metastatic breast cancer: VELVET Cohort 1 final results
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Safety and efficacy of vinorelbine in combination with pertuzumab and trastuzumab for first-line treatment of patients with HER2-positive locally advanced or metastatic breast cancer: VELVET Cohort 1 final results

机译:Vinorelbine与Pertuzumab和Trastuzumab组合的安全性和疗效与患有Her2阳性局部晚期或转移性乳腺癌患者的一线治疗:天鹅绒队队列1最终结果

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Pertuzumab, trastuzumab, and docetaxel is standard of care for first-line treatment of HER2-positive metastatic breast cancer (MBC). However, alternative chemotherapy partners are required to align with patient/physician preferences and to increase treatment flexibility. We report VELVET Cohort 1 results in which the efficacy and safety of pertuzumab and trastuzumab, administered sequentially in separate infusions, followed by vinorelbine, were evaluated. Cohort 2, where pertuzumab and trastuzumab were administered in a single infusion, followed by vinorelbine, recruited after Cohort 1 was fully enrolled, will be reported later. In this multicenter, two-cohort, open-label, phase II study, patients with HER2-positive locally advanced or MBC who had not received chemotherapy or biological therapy for their advanced disease received 3-weekly pertuzumab (840?mg loading, 420?mg maintenance doses) and trastuzumab (8?mg/kg loading, 6?mg/kg maintenance doses), followed by vinorelbine (25?mg/m2 initial dose, 30–35?mg/m2 maintenance doses) on days 1 and 8 or 2 and 9 of each 3-weekly cycle. Study treatment was given until investigator-assessed disease progression or unacceptable toxicity. The primary endpoint was investigator-assessed objective response rate (ORR) in patients with measurable disease at baseline per RECIST v1.1. Secondary endpoints included progression-free survival (PFS) and safety. Cohort 1 enrolled 106 patients. Investigator-assessed ORR was 74.2% (95% CI 63.8–82.9) in intent-to-treat patients with measurable disease (89/106 [84.0%]). Median PFS was 14.3?months (95% CI 11.2–17.5) in the intent-to-treat population. Treatment was reasonably well tolerated, with no unexpected toxicities. Diarrhea (61/106 patients [57.5%]) and neutropenia (54/106 [50.9%]) were the most common adverse events (AEs); neutropenia (33/106 [31.1%]) and leukopenia (14/106 [13.2%]) were the most common grade ≥3 AEs. Serious AEs were reported in 32/106 (30.2%) patients. AEs led to study drug discontinuation in 36/106 patients (34.0%). Eighteen of 106 patients (17.0%) had AEs suggestive of congestive heart failure; however, there were no confirmed cases. The vinorelbine, pertuzumab, and trastuzumab combination is active and reasonably well tolerated. This regimen offers an alternative for patients who cannot receive docetaxel for first-line treatment of HER2-positive locally advanced or MBC. ClinicalTrials.gov: NCT01565083 , registered on 26 March 2012.
机译:培妥珠单抗,曲妥珠单抗,和多西紫杉醇是护理标准为一线治疗HER2阳性转移性乳腺癌(MBC)的。然而,备选化疗伙伴必须与患者/医生的偏好和增加治疗灵活性对齐。我们报告丝绒队列1分的结果,其中的功效和帕妥珠单抗和曲妥单抗的安全性,在分开的输注依次施用,随后长春瑞滨,进行了评价。队列2,其中培妥珠单抗和曲妥单抗的单次输注施用,接着长春瑞滨,招募组1被完全登记后,将在后面的报道。在这个多,两队列,开放标签,II期临床研究中,患者为HER2阳性的局部晚期或MBC谁没有接受化疗或生物治疗进展性疾病接受3周帕妥珠单抗(840?mg负荷,420?毫克维持剂量)和曲妥珠单抗(8β毫克/千克加载,6?毫克/公斤的维持剂量),随后通过在1和8天长春瑞滨(25?毫克/米2的初始剂量,30-35?毫克/米2的维持剂量)或2,各3周周期的9。研究治疗给予直到研究者评估的疾病进展或不可接受的毒性。主要终点是在患者以每RECIST v1.1的基线可测量疾病研究者评估的客观响应率(ORR)。次要终点包括无进展生存期(PFS)和安全性。队列1登记106名患者。研究者评估的ORR为74.2%(95%CI 63.8-82.9)在意向治疗患有可测量的疾病(106分之89[84.0%])。中位PFS为在意向治疗人群14.3?个月(95%CI 11.2-17.5)。治疗合理的耐受性良好,没有意外的毒性。腹泻(61/106例[57.5%])和中性粒细胞减少(54/106 [50.9%])是最常见的不良事件(AE);中性粒细胞减少(106分之33[31.1%])和白细胞减少(106分之14[13.2%])是最常见的等级≥3的AEs。严重不良事件的报道中106分之32(30.2%)患者。 AE导致研究药物停药一百零六分之三十六例(34.0%)。的106例(17.0%)十八有不良暗示充血性心脏衰竭的;然而,没有确诊病例。长春瑞滨,帕妥珠单抗,曲妥珠单抗的组合是积极和合理的耐受性良好。该方案提供了患者的替代谁也不会收到一线治疗HER2阳性的多西他赛的局部晚期或MBC。 ClinicalTrials.gov:NCT01565083,2012年3月注册了26。

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