Pertuzumab Plus High-Dose Trastuzumab in Patients With Progressive Brain Metastases and HER2-Positive Metastatic Breast Cancer: Primary Analysis of a Phase II Study

被引:80
作者
Lin, Nancy U. [1 ]
Pegram, Mark [2 ]
Sahebjam, Solmaz [3 ]
Ibrahim, Nuhad [4 ]
Fung, Anita [5 ]
Cheng, Anna [5 ]
Nicholas, Alan [5 ]
Kirschbrown, Whitney [5 ]
Kumthekar, Priya [6 ]
机构
[1] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
[2] Stanford Comprehens Canc Inst, Palo Alto, CA USA
[3] Univ S Florida, Moffitt Canc Ctr, Tampa, FL 33620 USA
[4] MD Anderson Canc Ctr, Houston, TX USA
[5] Genentech Inc, San Francisco, CA 94080 USA
[6] Northwestern Univ, Chicago, IL 60611 USA
关键词
NERVOUS-SYSTEM METASTASES; TBCRC; 022; TRIAL; LAPATINIB; CAPECITABINE; NERATINIB; EFFICACY; CRITERIA; TUMORS; WOMEN;
D O I
10.1200/JCO.20.02822
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Effective therapies are needed for the treatment of patients with human epidermal growth factor receptor-2 (HER2)-positive metastatic breast cancer (MBC) with brain metastases. A trastuzumab radioisotope has been shown to localize in brain metastases of patients with HER2-positive MBC, and intracranial xenograft models have demonstrated a dose-dependent response to trastuzumab. METHODS In the phase II PATRICIA study (ClinicalTrials.gov identifier: ), patients with HER2-positive MBC with CNS metastases and CNS progression despite prior radiotherapy received pertuzumab plus high-dose trastuzumab (6 mg/kg weekly) until CNS or systemic disease progression or unacceptable toxicity. The primary end point was confirmed objective response rate (ORR) in the CNS per Response Assessment in Neuro-Oncology Brain Metastases criteria. Secondary end points included duration of response, clinical benefit rate (complete response plus partial response plus stable disease >= 4 or >= 6 months) in the CNS, and safety. RESULTS Thirty-nine patients were treated for a median (range) of 4.5 (0.3-37.3) months at clinical cutoff. Thirty-seven patients discontinued treatment, most commonly because of CNS progression (n = 27); two remained on treatment. CNS ORR was 11% (95% CI, 3 to 25), with four partial responses (median duration of response, 4.6 months). Clinical benefit rate at 4 months and 6 months was 68% and 51%, respectively. Two patients permanently discontinued study treatment because of adverse events (left ventricular dysfunction [treatment-related] and seizure, both grade 3). No grade 5 adverse events were reported. No new safety signals emerged with either agent. CONCLUSION Although the CNS ORR was modest, 68% of patients experienced clinical benefit, and two patients had ongoing stable intracranial and extracranial disease for > 2 years. High-dose trastuzumab for HER2-positive CNS metastases may warrant further study. (C) 2021 by American Society of Clinical Oncology
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收藏
页码:2667 / +
页数:12
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