Trastuzumab Deruxtecan in Patients With <i>HER2</i>-Mutant Metastatic Non–Small-Cell Lung Cancer: Primary Results From the Randomized, Phase II DESTINY-Lung02 Trial

Kōichi Goto(National Cancer Center Hospital East), Yasushi Goto(Tokyo National Hospital), Toshio Kubo(Okayama University Hospital), Kiichiro Ninomiya(Okayama University Hospital), Sang‐We Kim(Asan Medical Center), David Planchard(Institut Gustave Roussy), Myung‐Ju Ahn(Samsung Medical Center), Egbert F. Smit(Leiden University Medical Center), Adrianus J. de Langen(The Netherlands Cancer Institute), M. Pérol(Roche (Switzerland)), Elvire Pons‐Tostivint(Centre Hospitalier Universitaire de Nantes), Silvia Novello(Ospedale San Luigi Gonzaga), Hidetoshi Hayashi(Kindai University Hospital), Junichi Shimizu(Aichi Cancer Center), Dong‐Wan Kim(Seoul National University Hospital), Chih‐Hsi S. Kuo(Chang Gung University), James Chih‐Hsin Yang(National Taiwan University Hospital), Kaline Pereira(Daiichi Sankyo (United States)), Fu-Chih Cheng(Daiichi Sankyo (United States)), Ayumi Taguchi(Daiichi-Sankyo (Japan)), Yingkai Cheng(Daiichi Sankyo (United States)), Wenqin Feng(Daiichi Sankyo (United States)), Zenta Tsuchihashi(Daiichi Sankyo (United States)), Pasi A. Jänne(Dana-Farber Cancer Institute)
Journal of Clinical Oncology
September 11, 2023
Cited by 282Open Access
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Abstract

PURPOSE Trastuzumab deruxtecan (T-DXd) 5.4 and 6.4 mg/kg showed robust antitumor activity in multiple cancer indications; however, T-DXd 5.4 mg/kg has not been evaluated in patients with previously treated human epidermal growth factor receptor 2–mutant ( HER2m; defined as single-nucleotide variants and exon 20 insertions) metastatic non–small-cell lung cancer (mNSCLC). METHODS DESTINY-Lung02, a blinded, multicenter, phase II study, investigated T-DXd 5.4 mg/kg once every 3 weeks for the first time in previously treated (platinum-containing therapy) patients with HER2m mNSCLC and further assessed T-DXd 6.4 mg/kg once every 3 weeks in this population. The primary end point was confirmed objective response rate (ORR) per RECIST v1.1 by blinded independent central review. RESULTS One hundred fifty-two patients were randomly assigned 2:1 to T-DXd 5.4 or 6.4 mg/kg once every 3 weeks. As of December 23, 2022, the median duration of follow-up was 11.5 months (range, 1.1-20.6) with 5.4 mg/kg and 11.8 months (range, 0.6-21.0) with 6.4 mg/kg. Confirmed ORR was 49.0% (95% CI, 39.0 to 59.1) and 56.0% (95% CI, 41.3 to 70.0) and median duration of response was 16.8 months (95% CI, 6.4 to not estimable [NE]) and NE (95% CI, 8.3 to NE) with 5.4 and 6.4 mg/kg, respectively. Median treatment duration was 7.7 months (range, 0.7-20.8) with 5.4 mg/kg and 8.3 months (range, 0.7-20.3) with 6.4 mg/kg. Grade ≥ 3 drug-related treatment-emergent adverse events occurred in 39 of 101 (38.6%) and 29 of 50 (58.0%) patients with 5.4 and 6.4 mg/kg, respectively. 13 of 101 (12.9%) and 14 of 50 (28.0%) patients had adjudicated drug-related interstitial lung disease (2.0% grade ≥ 3 in each arm) with 5.4 and 6.4 mg/kg, respectively. CONCLUSION T-DXd demonstrated clinically meaningful responses at both doses. Safety profile was acceptable and generally manageable, favoring T-DXd 5.4 mg/kg.


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