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Purpose: To describe real-world characteristics and clinical outcomes among patients with HER2+ MBC receiving tucatinib-based treatments.
Methods: This retrospective study included patients diagnosed with HER2+ MBC between January 2017 and December 2022 from two administrative health claims databases, MerativeMarketScan and the Komodo Healthcare Map. Patient characteristics were captured at baseline (≤ 6 months prior to tucatinib initiation). Outcomes were assessed starting from tucatinib-based treatment initiation and included real-world time to discontinuation (rwTTD) and treatment persistence.
Results: There were 150 patients in MarketScan who received tucatinib-based therapy: median (IQR) prior lines of therapy (LOT) was 2 (2-4) and 110 patients (73.3%) had brain metastases. 436 patients in Komodo received tucatinib-based therapy: median (IQR) prior LOTs were 2 (1-3), and 307 (70.4%) had brain metastases. Median (95% CI) rwTTD was 7.4 (5.0-13.1) months in MarketScan (median follow-up 9.7 months) and 9.0 (7.4-9.8) months in Komodo (median follow-up 10.3 months). In patients who received tucatinib in combination with trastuzumab and capecitabine immediately following trastuzumab deruxtecan (T-DXd) and after ≥ 2 prior HER2-directed therapies (MarketScan: n = 26, median prior LOT 4; Komodo: n = 34, median prior LOT 3), median (95% CI) rwTTD was 5.5 (3.4-not reached [NR]) months in MarketScan and 4.8 (3.2-NR) months in Komodo.
Conclusion: These results reinforce the real-world effectiveness of tucatinib in patients with HER2+ MBC, including patients with prior T-DXd treatment. Further research is needed to determine the optimal treatment sequencing for patients with HER2+ MBC.
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http://dx.doi.org/10.1007/s10147-025-02800-7 | DOI Listing |
Purpose: To describe real-world characteristics and clinical outcomes among patients with HER2+ MBC receiving tucatinib-based treatments.
Methods: This retrospective study included patients diagnosed with HER2+ MBC between January 2017 and December 2022 from two administrative health claims databases, MerativeMarketScan and the Komodo Healthcare Map. Patient characteristics were captured at baseline (≤ 6 months prior to tucatinib initiation).
Cancer Control
April 2025
Division of Hematology and Oncology, University of Vermont Medical Center, Burlington, VT, USA.
Tucatinib is an oral human epidermal growth factor receptor 2 (HER2)-targeted therapy approved by the European Medicines Agency (EMA) for use in combination with trastuzumab and capecitabine for patients with HER2 + locally advanced or metastatic breast cancer (MBC) treated with ≥2 prior HER2-directed regimens. This real-world study describes patient characteristics and clinical outcomes with tucatinib after receiving ≥2 HER2-targeted therapies in the metastatic setting. This study included patients diagnosed with HER2 + MBC (between January 2017 and December 2022) who received tucatinib after ≥2 HER2-directed therapies in the metastatic setting in a US-based nationwide, de-identified electronic health record-derived MBC database.
View Article and Find Full Text PDFExpert Opin Investig Drugs
March 2025
Department of Hematology and Oncology, Mayo Clinic, Arizona, AZ, USA.
Introduction: Over the past 20 years, the treatment landscape of HER2-amplified tumors has considerably evolved. Until now, no approved targeted therapies were available for patients with HER2-amplified metastatic colorectal cancer (mCRC). Tucatinib, a highly selective tyrosine kinase inhibitor, demonstrated significant efficacy in combination with trastuzumab in patients with refractory mCRC, leading to its approval by the Food and Drug Administration (FDA).
View Article and Find Full Text PDFEur J Cancer
July 2023
Department of Medical Oncology, Georges-François Leclerc Centre, 1 rue du Professeur Marion, 21000 Dijon, France; Platform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France; University of Burgundy-Franche Comté, 21000 Dijon, France; INSERM U1231, 21000 Di
Mil Med Res
July 2022
Department of Pharmacology and Toxicology, Boonshoft School of Medicine Wright State University, Dayton, OH, 45435, USA.
Overexpression of human epidermal growth factor receptor 2 (HER2) occurs in approximately 15-20% of breast cancer cases. HER2 is a member of the epidermal growth factor receptor (EGFR) family with tyrosinase kinase activity, and its overexpression is linked to poor prognosis and shorter progression-free survival (PFS) and overall survival (OS). Among various treatment options, HER2-targeting monoclonal antibodies and tyrosine kinase inhibitors (TKIs) have mostly been applied in recent decades to treat HER2-positive (HER2+) breast cancer patients.
View Article and Find Full Text PDF