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Treatment with trastuzumab deruxtecan in patients with HER2-positive breast cancer and brain metastases and/or leptomeningeal disease (ROSET-BM)

Therapeutic options for breast cancer patients with brain metastases (BM)/leptomeningeal carcinomatosis (LMC) are limited. Here, we report on the effectiveness and safety of trastuzumab deruxtecan (T-DXd) in human epidermal growth factor receptor 2-positive breast cancer patients with BM. Data were...

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Detalles Bibliográficos
Autores principales: Niikura, Naoki, Yamanaka, Takashi, Nomura, Hironori, Shiraishi, Kazuhiro, Kusama, Hiroki, Yamamoto, Mitsugu, Matsuura, Kazuo, Inoue, Kenichi, Takahara, Sachiko, Kita, Shosuke, Yamaguchi, Miki, Aruga, Tomoyuki, Shibata, Nobuhiro, Shimomura, Akihiko, Ozaki, Yuri, Sakai, Shuji, Kiga, Yoko, Izutani, Tadahiro, Shiosakai, Kazuhito, Tsurutani, Junji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567705/
https://www.ncbi.nlm.nih.gov/pubmed/37821514
http://dx.doi.org/10.1038/s41523-023-00584-5
Descripción
Sumario:Therapeutic options for breast cancer patients with brain metastases (BM)/leptomeningeal carcinomatosis (LMC) are limited. Here, we report on the effectiveness and safety of trastuzumab deruxtecan (T-DXd) in human epidermal growth factor receptor 2-positive breast cancer patients with BM. Data were analyzed for 104 patients administered T-DXd. Overall response rate (ORR), progression-free survival (PFS), overall survival (OS), intracranial (IC)-ORR, and IC-PFS were evaluated. ORR by investigator assessment was 55.7% (total population). Median PFS was 16.1 months; 12-month OS rate was 74.9% (total population). Median time-to-treatment failure was 9.7 months. In 51 patients with BM imaging, IC-ORR and median IC-PFS by independent central review were 62.7% and 16.1 months, respectively. In 19 LMC patients, 12-month PFS and OS rates were 60.7% and 87.1%, respectively. T-DXd showed effectiveness regarding IC-ORR, IC-PFS, PFS, and OS in breast cancer patients with BM/active BM, and sustained systemic and central nervous system disease control in LMC patients. Trial Registration: UMIN000044995.