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Concurrent Lapatinib With Brain Radiation Therapy in Patients With HER2+Breast Cancer With Brain Metastases: NRG Oncology - KROG/ RTOG 1119 Phase 2 Randomized Trial

Authors
 In Ah Kim  ;  Kathryn A Winter  ;  Paul W Sperduto  ;  Jennifer F De Los Santos  ;  David M Peereboom  ;  Tomi Ogunleye  ;  Daniel Boulter  ;  Joel M Fritz  ;  Kwan Ho Cho  ;  Kyung Hwan Shin  ;  Imran Zoberi  ;  Serah Choi  ;  Joshua D Palmer  ;  Ben Liem  ;  Yong Bae Kim  ;  Bethany M Anderson  ;  Anupama W Thakrar  ;  Thierry M Muanza  ;  Michelle M Kim  ;  Doo Ho Choi  ;  Minesh P Mehta  ;  Julia R White 
Citation
 INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, Vol.118(5) : epub-1401, 2024-04 
Journal Title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
ISSN
 0360-3016 
Issue Date
2024-04
MeSH
Brain / pathology ; Brain Neoplasms* / radiotherapy ; Brain Neoplasms* / secondary ; Breast Neoplasms* / pathology ; Female ; Humans ; Lapatinib ; Radiosurgery* / methods
Abstract
Purpose: Lapatinib plus whole brain radiation therapy (WBRT) or stereotactic radiosurgery (SRS) was hypothesized to improve the 12-week intracranial complete response (CR) rate compared with either option of radiation therapy (RT) alone for patients with brain metastases (BM) from human epidermal growth factor receptor 2-positive (HER2+) breast cancer.

Methods and materials: This study included patients with HER2+ breast cancer with ≥1 measurable, unirradiated BM. Patients were randomized to WBRT (37.5 Gy/3 wk)/SRS (size-based dosing) ± concurrent lapatinib (1000 mg daily for 6 weeks). Secondary endpoints included objective response rate (ORR), lesion-specific response, central nervous system progression-free survival, and overall survival.

Results: From July 2012 to September 2019, 143 patients were randomized, with 116 analyzable for the primary endpoint. RT + lapatinib did not improve 12-week CR (0% vs 6% for RT alone, 1-sided P = .97), or ORR at 12 weeks. At 4 weeks, RT + lapatinib showed higher ORR (55% vs 42%). Higher graded prognostic assessment and ≤10 lesions were associated with higher 12-week ORR. Grade 3 and 4 adverse event rates were 8% and 0% for RT and 28% and 6% for RT + lapatinib.

Conclusions: The addition of 6 weeks of concomitant lapatinib to WBRT/SRS did not improve the primary endpoint of 12-week CR rate or 12-week ORR. Adding lapatinib to WBRT/SRS showed improvement of 4-week ORR, suggesting a short-term benefit from concomitant therapy.
Full Text
https://www.sciencedirect.com/science/article/pii/S0360301623076812
DOI
10.1016/j.ijrobp.2023.07.019
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
Yonsei Authors
Kim, Yong Bae(김용배) ORCID logo https://orcid.org/0000-0001-7573-6862
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/202022
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