TROPION-Lung08: phase III study of datopotamab deruxtecan plus pembrolizumab as first-line therapy for advanced NSCLC

Author:

Levy Benjamin P1,Felip Enriqueta2ORCID,Reck Martin3ORCID,Yang James CH4ORCID,Cappuzzo Federico5,Yoneshima Yasuto6,Zhou Caicun7,Rawat Siddhartha8,Xie Jingdong8,Basak Priyanka8,Xu Lu910,Sands Jacob11ORCID

Affiliation:

1. The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Medicine, Washington, DC 20016, USA

2. Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, Barcelona, 08035, Spain

3. Lung Clinic Grosshansdorf, Airway Research Center North (ARCN), Grosshansdorf, 22927, Germany

4. Department of Oncology, National Taiwan University Hospital, Taipei, 106, Taiwan

5. Istituto Nazionale Tumori Regina Elena, Rome, 00144, Italy

6. Department of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, 812-8582, Japan

7. Department of Oncology, Shanghai Pulmonary Hospital & Thoracic Cancer Institute, School of Medicine, Tongji University, Shanghai, 200092, China

8. Daiichi Sankyo, Inc, Basking Ridge, NJ 07920, USA

9. Merck & Co., Inc., Rahway, NJ 07065, USA

10. AstraZeneca, Gaithersburg, MD 20878, USA

11. Dana-Farber Cancer Institute, Boston, MA 02215, USA

Abstract

Pembrolizumab monotherapy is a standard first-line treatment for PD-L1–high advanced non-small-cell lung cancer (NSCLC) without actionable genomic alterations (AGA). However, few patients experience long-term disease control, highlighting the need for more effective therapies. Datopotamab deruxtecan (Dato-DXd), a novel trophoblast cell-surface antigen 2-directed antibody–drug conjugate, showed encouraging safety and antitumor activity with pembrolizumab in advanced NSCLC. We describe the rationale and design of TROPION-Lung08, a phase III study evaluating safety and efficacy of first-line Dato-DXd plus pembrolizumab versus pembrolizumab monotherapy in patients with advanced/metastatic NSCLC without AGAs and with PD-L1 tumor proportion score ≥50%. Primary end points are progression-free survival and overall survival; secondary end points include objective response rate, duration of response, safety and presence of antidrug antibodies. Clinical trial registration: NCT05215340 ( ClinicalTrials.gov )

Funder

Daiichi Sankyo, Inc.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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