Brain Radiotherapy With Pyrotinib and Capecitabine in Patients With ERBB2-Positive Advanced Breast Cancer and Brain Metastases

Author:

Yang Zhaozhi123,Meng Jin123,Mei Xin123,Mo Miao4,Xiao Qin5,Han Xu123,Zhang Li123,Shi Wei123,Chen Xingxing1,Ma Jinli123,Palmer Joshua6,Shao Zhimin7,Zhang Zhen123,Yu Xiaoli123,Guo Xiaomao123

Affiliation:

1. Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China

2. Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

3. Clinical Research Center for Radiation Oncology, Shanghai Key Laboratory of Radiation Oncology, Shanghai, China

4. Department of Cancer Prevention, Fudan University Shanghai Cancer Center, Shanghai, China

5. Department of Radiology, Fudan University Shanghai Cancer Center, Shanghai, China

6. The James Cancer Center at The Ohio State University, Columbus

7. Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, China

Abstract

ImportanceThe potential benefit of combining intracranial effective systemic therapy with radiotherapy for patients with breast cancer with brain metastases remains unclear.ObjectiveTo assess the activity and safety of combining radiotherapy with pyrotinib and capecitabine in patients with ERBB2-positive breast cancer and brain metastases.Design, Setting, and ParticipantsThis was a single-arm, single-center, phase 2 nonrandomized clinical trial with a safety run-in phase. Between January 2020 and August 2022, patients with ERBB2-positive breast cancer and brain metastases were enrolled. The data cutoff date was February 1, 2023.InterventionsPatients received either fractionated stereotactic radiotherapy or whole-brain radiotherapy. Treatment with pyrotinib (400 mg, once daily) and capecitabine (1000 mg/m2, twice daily, on days 1-14 of each 21-day cycle) was initiated from the first day of radiotherapy to the seventh day after the completion of radiotherapy and continued until disease progression or unacceptable toxic effects.Main Outcomes and MeasuresThe primary end point was 1-year central nervous system (CNS) progression-free survival (PFS) rate. Secondary end points included CNS objective response rate (ORR), PFS, overall survival (OS), safety, and changes in neurocognitive function.ResultsA total of 40 female patients (median age, 50.5 years [IQR, 46-59 years]) were enrolled and received treatment, including 3 patients in safety run-in phase. With a median follow-up of 17.3 months (IQR, 10.3-26.9), the 1-year CNS PFS rate was 74.9% (95% CI, 61.9%-90.7%), and the median CNS PFS was 18.0 months (95% CI, 15.5 to not reached). The 1-year PFS rate was 66.9% (95% CI, 53.1%-84.2%), and the median PFS was 17.6 months (95% CI, 12.8-34.1). The CNS objective response rate was 85% (34 of 40). Median overall survival was not reached. The most common grade 3 or 4 treatment-related adverse event was diarrhea (7.5%). Asymptomatic radiation necrosis was identified in 4 of 67 lesions (6.0%) treated with fractionated stereotactic radiotherapy. Most patients maintained neurocognitive function, as evaluated by the Mini-Mental State Examination at different points.Conclusions and RelevanceThe results of this trial suggest that radiotherapy combined with pyrotinib and capecitabine is associated with long intracranial survival benefit in patients with ERBB2-positive advanced breast cancer and brain metastases with an acceptable safety profile. This combination deserves further validation.Trial RegistrationClinicalTrials.gov Identifier: NCT04582968

Publisher

American Medical Association (AMA)

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A review of therapeutic agents for breast cancer with potentially radiosensitizing properties;Radiation Medicine and Protection;2024-06

2. Gray oncologic areas;Journal of Surgical Oncology;2024-02-06

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