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Trastuzumab deruxtecan in metastatic breast cancer with variable HER2 expression: the phase 2 DAISY trial.

Authors :
Mosele F
Deluche E
Lusque A
Le Bescond L
Filleron T
Pradat Y
Ducoulombier A
Pistilli B
Bachelot T
Viret F
Levy C
Signolle N
Alfaro A
Tran DTN
Garberis IJ
Talbot H
Christodoulidis S
Vakalopoulou M
Droin N
Stourm A
Kobayashi M
Kakegawa T
Lacroix L
Saulnier P
Job B
Deloger M
Jimenez M
Mahier C
Baris V
Laplante P
Kannouche P
Marty V
Lacroix-Triki M
Diéras V
André F
Source :
Nature medicine [Nat Med] 2023 Aug; Vol. 29 (8), pp. 2110-2120. Date of Electronic Publication: 2023 Jul 24.
Publication Year :
2023

Abstract

The mechanisms of action of and resistance to trastuzumab deruxtecan (T-DXd), an anti-HER2-drug conjugate for breast cancer treatment, remain unclear. The phase 2 DAISY trial evaluated the efficacy of T-DXd in patients with HER2-overexpressing (n = 72, cohort 1), HER2-low (n = 74, cohort 2) and HER2 non-expressing (n = 40, cohort 3) metastatic breast cancer. In the full analysis set population (n = 177), the confirmed objective response rate (primary endpoint) was 70.6% (95% confidence interval (CI) 58.3-81) in cohort 1, 37.5% (95% CI 26.4-49.7) in cohort 2 and 29.7% (95% CI 15.9-47) in cohort 3. The primary endpoint was met in cohorts 1 and 2. Secondary endpoints included safety. No new safety signals were observed. During treatment, HER2-expressing tumors (n = 4) presented strong T-DXd staining. Conversely, HER2 immunohistochemistry 0 samples (n = 3) presented no or very few T-DXd staining (Pearson correlation coefficient r = 0.75, P = 0.053). Among patients with HER2 immunohistochemistry 0 metastatic breast cancer, 5 of 14 (35.7%, 95% CI 12.8-64.9) with ERBB2 expression below the median presented a confirmed objective response as compared to 3 of 10 (30%, 95% CI 6.7-65.2) with ERBB2 expression above the median. Although HER2 expression is a determinant of T-DXd efficacy, our study suggests that additional mechanisms may also be involved. (ClinicalTrials.gov identifier NCT04132960 .).<br /> (© 2023. The Author(s).)

Details

Language :
English
ISSN :
1546-170X
Volume :
29
Issue :
8
Database :
MEDLINE
Journal :
Nature medicine
Publication Type :
Academic Journal
Accession number :
37488289
Full Text :
https://doi.org/10.1038/s41591-023-02478-2