Background: VELVET Cohort 1 demonstrated the applicability of pertuzumab, trastuzumab, and vinorelbine as an alternative first-line treatment regimen for patients with HER2-positive locally advanced or metastatic breast cancer (MBC) who cannot receive docetaxel. Co-infusion of pertuzumab and trastuzumab may reduce clinic time and medical resource utilization. We report results from Cohort 2, in which pertuzumab and trastuzumab were co-infused, followed by vinorelbine.
Patients and methods: During cycle 1, patients with HER2-positive locally advanced or MBC received loading doses of pertuzumab (840 mg) and trastuzumab (8 mg/kg) on consecutive days, followed by vinorelbine (25 mg/m2) on days two and nine. From cycle 2 onwards, patients received a co-infusion of pertuzumab (420 mg) and trastuzumab (6 mg/kg) on day one, followed by vinorelbine (30-35 mg/m2) on days one and eight (or days two and nine). The primary endpoint was objective response rate (ORR) in patients with measurable disease. Secondary endpoints included progression-free survival (PFS) and safety.
Results: Cohort 2 enrolled 107 patients. The ORR was 63.7% (95% confidence interval [CI] 53.0-73.6) in patients with measurable disease (91/107; 85.0%). Median PFS was 11.5 months (95% CI 10.3-15.8). The most common adverse events [AEs] were diarrhea (57.9%), neutropenia (57.0%), and nausea (41.1%). Grade ≥3 AEs occurred in 85 patients (79.4%) and serious AEs in 44 patients (41.1%). Eighteen patients (16.8%) had AEs suggestive of congestive heart failure.
Conclusion: These results support the feasibility of pertuzumab and trastuzumab co-infusion from a safety perspective and support Cohort 1 conclusions that vinorelbine offers an alternative chemotherapy companion for pertuzumab and trastuzumab. The Oncologist 2017;22:1160-1168 IMPLICATIONS FOR PRACTICE: Combined treatment with pertuzumab, trastuzumab, and docetaxel is the standard of care for first-line HER2-positive metastatic breast cancer. However, some patients cannot, or choose not to, receive docetaxel. VELVET Cohort 2 results support the results from Cohort 1 that suggest that pertuzumab plus trastuzumab and vinorelbine is a suitable alternative for these patients. In addition to this, results from Cohort 2 support the feasibility of administering pertuzumab and trastuzumab together in a single infusion bag, which has the potential to offer greater patient convenience and reduce active health care professional time and medical resource utilization compared with administering them separately.
摘要
背景. VELVET队列1证明, 无法接受多西他赛的HER2阳性局部晚期或转移性乳腺癌(MBC)患者可以使用帕妥珠单抗、曲妥珠单抗和长春瑞滨作为替代一线治疗方案。帕妥珠单抗和曲妥珠单抗联合输注可节约门诊时间并减少医疗资源利用。本文报告了队列2的结果;该队列联合输注帕妥珠单抗与曲妥珠单抗, 随后注射长春瑞滨。
患者和方法. 在第1周期, HER2阳性局部晚期或MBC患者在连续2天内先后接受负荷剂量的帕妥珠单抗(840 mg)和曲妥珠单抗(8 mg/kg), 随后分别于第2天和第9天接受长春瑞滨(25 mg/m2)。从第2周期开始, 患者在第1天联合输注帕妥珠单抗(420 mg)和曲妥珠单抗(6 mg/kg), 随后分别于第1天和第8天(或第2天和第9天)接受长春瑞滨(30–35 mg/m2)。主要终点为病灶可测量患者中的客观缓解率(ORR)。次要终点包括无进展生存期(PFS)和安全性。
结果. 队列2入组了107例患者。病灶可测量患者(91/107;85.0%)的ORR为63.7%[95%置信区间(CI):53.0‐73.6]。中位PFS为11.5个月(95%CI:10.3‐15.8)。最常见的不良事件(AE)为腹泻(57.9%)、中性粒细胞减少症(57.0%)和恶心(41.1%)。85例患者(79.4%)发生≥3级AE, 44例患者(41.1%)发生严重AE。18例患者(16.8%)发生提示充血性心力衰竭的AE。
结论. 上述结果从安全性角度支持了帕妥珠单抗与曲妥珠单抗联合输注的可行性, 并且印证了队列1的结论, 即长春瑞滨可作为帕妥珠单抗与曲妥珠单抗的候选联合化疗药物
Keywords: HER2-positive; Metastatic breast cancer; Pertuzumab; Trastuzumab; Vinorelbine.
© 2017 The Authors. The Oncologist published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.