Trastuzumab deruxtecan for the treatment of patients with HER2-positive breast cancer with brain and/or leptomeningeal metastases: an updated overall survival analysis using data from a multicenter retrospective study (ROSET-BM)
- PMID: 39133378
- PMCID: PMC11489233
- DOI: 10.1007/s12282-024-01614-1
Trastuzumab deruxtecan for the treatment of patients with HER2-positive breast cancer with brain and/or leptomeningeal metastases: an updated overall survival analysis using data from a multicenter retrospective study (ROSET-BM)
Erratum in
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Correction: Trastuzumab deruxtecan for the treatment of patients with HER2-positive breast cancer with brain and/or leptomeningeal metastases: an updated overall survival analysis using data from a multicenter retrospective study (ROSET-BM).Breast Cancer. 2024 Nov;31(6):1184. doi: 10.1007/s12282-024-01632-z. Breast Cancer. 2024. PMID: 39302559 Free PMC article. No abstract available.
Abstract
We provide updated results (median follow-up duration: 20.4 months) of a retrospective study on the effectiveness of trastuzumab deruxtecan (T-DXd) in patients with human epidermal growth factor receptor 2-positive (HER2+) breast cancer with brain metastases (BM) and/or leptomeningeal disease (ROSET-BM). Median progression-free survival (PFS) was 14.6 months. Median overall survival (OS) was not reached (NR); 24-month OS rate was 56.0%. Subgroup analysis showed that median PFS was 13.2 months in patients with analytical active BM, 17.5 months in patients with leptomeningeal carcinomatosis (LMC), and NR in patients with analytical stable BM (24-month PFS rates in patients with analytical active BM, LMC, and analytical stable BM were 32.7%, 25.1%, and 60.8%, respectively). Median OS was 27.0 months in patients with analytical active BM and NR in patients with LMC or analytical stable BM (24-month OS rates in patients with analytical active BM, LMC, and analytical stable BM were 52.0%, 61.6%, and 71.6%, respectively). The most common adverse event leading to discontinuation of T-DXd was interstitial lung disease (ILD; 23.1%); median ILD onset time among patients who discontinued T-DXd treatment due to ILD was 5.3 months. T-DXd has promising effectiveness in heavily pre-treated HER2+ metastatic breast cancer patients with BM and LMC. The incidence and median onset time of ILD were similar to those of Japanese subgroups in previous studies.
Keywords: Brain metastasis; Breast cancer; HER2+; Leptomeningeal; Trastuzumab deruxtecan.
© 2024. The Author(s).
Conflict of interest statement
TN has received personal fees from Chugai Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Daiichi Sankyo Co., Ltd., AstraZeneca K.K., Taiho Pharmaceutical Co., Ltd., Eisai Co., Ltd., Pfizer Japan Inc., MSD K.K., Novartis Pharma K.K., Sandoz K.K., and Celltrion Inc. NN reports consulting or advisory roles for AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., and Daiichi Sankyo Co., Ltd.; and has received lecture fees from AstraZeneca K.K., Eisai Co., Ltd., Pfizer Japan Inc., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Eli Lilly Japan K.K., and Nippon Kayaku Co., Ltd.; and has received research funding from Pfizer Japan Inc., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Eli Lilly Japan K.K., and Nippon Kayaku Co., Ltd. TY has received lecture fees from AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K.K., Kyowa Kirin Co., Ltd., Novartis Pharma K.K., and Pfizer Japan Inc. KI has received research funding from Daiichi Sankyo Co., Ltd., AstraZeneca K.K., Chugai Pharmaceutical Co., Ltd., MSD K.K., and Ono Pharmaceutical Co., Ltd. M Yamaguchi has received speakers’ bureau from Pfizer Japan Inc., Novartis Pharma K.K., Taiho Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Medicon, Inc., Kyowa Kirin Co., Ltd., Chugai Pharmaceutical Co., Ltd., and Daiichi Sankyo Co., Ltd. TA has received speakers’ bureau from Chugai Pharmaceutical Co., Ltd., Pfizer Japan Inc., Eli Lilly Japan K.K., and AstraZeneca K.K. NS reports consulting or advisory roles for Kyowa Kirin Co., Ltd. and Chugai Pharmaceutical Co., Ltd.; and has received speakers’ bureau from Daiichi Sankyo Co., Ltd., Kyowa Kirin Co., Ltd., Pfizer Japan Inc., Eisai Co., Ltd., Yakult Honsha Co., Ltd., Taiho Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., AstraZeneca K.K., Merck Biopharma Co., Ltd., Bayer Yakuhin, Ltd., Eli Lilly Japan K.K., Ono Pharmaceutical Co., Ltd., and Nippon Kayaku Co., Ltd.; and has received research funding from Daiichi Sankyo Co., Ltd., Ono Pharmaceutical Co., Ltd., and MSD K.K. JT reports consulting or advisory roles for Daiichi Sankyo Co., Ltd., AstraZeneca K.K., Eisai Co., Ltd., Eli Lilly Japan K.K., and Seagen Inc.; and has received speakers’ bureau from Daiichi Sankyo Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K.K., and Kyowa Kirin Co., Ltd.; and has received research funding from Daiichi Sankyo Co., Ltd., AstraZeneca K.K., Eisai Co., Ltd., Eli Lilly Japan K.K., Seagen Inc., Kyowa Kirin Co., Ltd., Sant Joan de Déu Research Foundation, and West Japan Oncology Group. DT, TT, AB, and KS are employees of Daiichi Sankyo Co., Ltd. M Yamamoto, KM, ST, HN, SK, AS, YO, and SS have no conflicts of interest to disclose.
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References
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