Abstract 1507TiP
Background
T-DXd is a HER2-directed antibody-drug conjugate available for the treatment of pts with metastatic NSCLC with activating HER2 mutations, HER2+ breast or gastric cancer, or HER2-low breast cancer. DESTINY-Lung01 showed efficacy of T-DXd monotherapy in heavily pretreated pts with unresectable/metastatic, HER2-OE, nonsquamous NSCLC. In preclinical studies, the combination of T-DXd and immunotherapy was more effective than either therapy alone, and the addition of chemotherapy may improve efficacy. This trial is evaluating T-DXd alone or in combination with durvalumab (durva) or MEDI5752 (a PD-1/CTLA-4 bispecific antibody) with or without chemotherapy in pts with unresectable/metastatic, HER2-OE, nonsquamous NSCLC.
Trial design
DESTINY-Lung03 (NCT04686305) is a phase 1b, open-label, multicenter, dose-escalation and -expansion study in pts with HER2-OE unresectable, locally advanced or metastatic, nonsquamous NSCLC. In part 1 (enrollment completed), pts with disease progression after 1 or 2 lines of systemic therapy in the recurrent/metastatic setting receive T-DXd monotherapy or T-DXd + durva in combination with cisplatin, carboplatin, or pemetrexed. Part 2 of the trial was not initiated. In part 3, pts who have not received prior treatment for advanced or metastatic disease will receive T-DXd in combination with MEDI5752, with or without carboplatin; pts in this phase must not have a history of prior immunotherapy for early disease and must lack activating EGFR mutations, an EML4-ALK fusion, or other targetable alterations. The primary endpoint is the frequency of adverse events (AEs) and serious AEs (SAEs) with T-DXd + durva + chemotherapy (part 1) or T-DXd + MEDI5752 ± chemotherapy (part 3). Secondary endpoints include confirmed objective response rate, duration of response, disease control rate, progression-free and overall survival, pharmacokinetics, and immunogenicity in all arms as well as the frequency of AEs and SAEs with T-DXd monotherapy (part 1).
Clinical trial identification
NCT04686305.
Editorial acknowledgement
Medical writing support was provided by Articulate Science, LLC, and was funded by AstraZeneca in accordance with Good Publication Practice (GPP) guidelines.
Legal entity responsible for the study
AstraZeneca and Daiichi Sankyo.
Funding
AstraZeneca in collaboration with Daiichi Sankyo.
Disclosure
D. Planchard: Financial Interests, Personal, Speaker, Consultant, Advisor: AstraZeneca, Bristol Myers Squibb, Boehringer Ingelheim, Celgene, Daiichi Sankyo, Eli Lilly, Merck, Novartis, Pfizer, prIME Oncology, Peer CME, Roche, Janssen, AbbVie, Seagen, Gilead; Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, Bristol Myers Squibb, Boehringer Ingelheim, Celgene, Daiichi Sankyo, Eli Lilly, Merck, Novartis, Pfizer, prIME Oncology, Peer CME, Roche, Janssen, AbbVie; Financial Interests, Personal, Other, meetings and/or travel: AstraZeneca, Roche, Novartis, Pfizer; Financial Interests, Personal, Advisory Board: AstraZeneca, Bristol Myers Squibb, Boehringer Ingelheim, Celgene, Daiichi Sankyo, Eli Lilly, Merck, Novartis, Pfizer, prIME Oncology, Peer CME, Roche, Janssen, AbbVie; Financial Interests, Institutional, Other, Clinical trials research as principal or co-investigator: AstraZeneca, Bristol Myers Squibb, Boehringer Ingelheim, Eli Lilly, Merck, Novartis, Pfizer, Roche, MedImmune, Sanofi-Aventis, Taiho Pharma, Novocure, Daiichi Sankyo, Janssen, AbbVie. J.R. Brahmer: Financial Interests, Personal, Advisory Role: Bristol Myers Squibb, Eli Lilly, Merck, Amgen, Genentech, GSK, AstraZeneca, Regeneron, Sanofi; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Bristol Myers Squibb, Roche/Genentech; Financial Interests, Institutional, Research Funding: Bristol Myers Squibb, AstraZeneca, Spectrum Pharmaceuticals, Revolution, Rapt Therapeutics, Genentech/Roche. J.C. Yang: Financial Interests, Personal, Advisory Role: Boehringer Ingelheim, Novartis, AstraZeneca, Clovis Oncology, Eli Lilly, MSD Oncology, Merck Serono, Celgene, Bayer, Pfizer, Ono Pharmaceutical, Bristol Myers Squibb, Yuhan, Hansoh, Blueprint Medicines, Daiichi Sankyo, G1 Therapeutics, AbbVie, Takeda, Amgen, Incyte; Financial Interests, Institutional, Advisory Role: Boehringer Ingelheim, Merck Serono, Janssen, GSK, Amgen, Takeda, Daiichi Sankyo, AstraZeneca, Novartis, MSD Oncology; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Pfizer; Financial Interests, Personal, Other, Honoraria: Boehringer Ingelheim, Roche, MSD, AstraZeneca, Novartis, Bristol Myers Squibb, Ono Pharmaceutical, Takeda, Eli Lilly, Pfizer. R.K. Li: Financial Interests, Institutional, Principal Investigator: AstraZeneca, Roche, Arcus, BeiGene; Financial Interests, Personal, Other, Payment or honoraria for lectures, presentations, speakers bureaus, abstract writing or educational events: AstraZeneca, Roche, Eisai; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Other, Support for attending meetings and/or travel: Eisai. J. Han: Financial Interests, Institutional, Research Funding: Pfizer, Ono, Takeda, Roche; Financial Interests, Institutional, Principal Investigator: AstraZeneca, Amgen, AbbVie, Janssen, GSK, Gilead; Financial Interests, Personal, Speaker, Consultant, Advisor: AstraZeneca, Janssen, Amgen, Novartis, Merck, Abion, J Ints Bio; Financial Interests, Personal, Other, Payment or honoraria for lectures, presentations, speakers bureaus, abstract writing or educational events: AstraZeneca, Janssen, Merck, Yuhan, Novartis , Pfizer; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Membership or affiliation: ASCO, AACR, ESMO, KCA. D.L. Cortinovis: Financial Interests, Personal, Advisory Board, fee for consulting activity: MSD, BMS, Roche, Sanofi Genzyme, Amgen, AstraZeneca, Novartis. Y. Runglodvatana: Financial Interests, Personal, Principal Investigator: AstraZeneca, Roche, Arcus, BeiGene; Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, Roche, Eisai; Financial Interests, Personal, Other, attending meetings and/or travel: Eisai; Financial Interests, Personal, Advisory Board: AstraZeneca. E. Nakajima: Financial Interests, Personal, Full or part-time Employment: AstraZeneca, US Food and Drug Administration, MedStar Georgetown University; Financial Interests, Personal, Other, Support for attending meetings and/or travel: US Food and Drug Administration; Financial Interests, Personal, Membership or affiliation: ASCO. A. Ragone: Financial Interests, Personal, Full or part-time Employment: AstraZeneca. M. Winter: Financial Interests, Personal, Full or part-time Employment: AstraZeneca; Financial Interests, Personal, Stocks or ownership: AstraZeneca. M. Gustavson: Financial Interests, Personal, Full or part-time Employment: AstraZeneca; Financial Interests, Personal, Stocks or ownership: AstraZeneca. All other authors have declared no conflicts of interest.
Resources from the same session
1478P - Circulating pre-treatment T-Cell receptor repertoire as a predictive biomarker in non-small cell lung cancer patients treated with pembrolizumab
Presenter: Elin Gray
Session: Poster session 21
1479P - Association between high baseline low density neutrophils and resistance to immunotherapy in untreated non-small cell lung cancer: Molecular characterization of low-density neutrophils
Presenter: Hugo Arasanz
Session: Poster session 21
1480P - Integrating the on-treatment mGPS improves prognostic accuracy of imaging-based staging in patients with non-small-cell lung cancer (NSCLC) treated with immune-checkpoint inhibitors
Presenter: Jonas Saal
Session: Poster session 21
1481P - Singular immune-related adverse events and efficacy outcomes of immune checkpoint inhibitors in advanced non-small cell lung cancer
Presenter: Jose Miguel Jurado García
Session: Poster session 21
1482P - Multicenter pharmacokinetic study of pembrolizumab for non-small cell lung cancer in elderly adults aged over 75 years
Presenter: Jun Sakakibara-Konishi
Session: Poster session 21
1483P - Challenge of systemic first-line treatment of elderly lung cancer patients
Presenter: Konstantinos Ferentinos
Session: Poster session 21
1484P - Impact of concomitant KRAS/STK11 or KRAS/KEAP1 mutations on response to immune checkpoint inhibition in NSCLC: A real-world data analysis
Presenter: Louisa Hempel
Session: Poster session 21
1485P - Systemic inflammatory index dynamics at 6 weeks as an early surrogate for clinical benefit in patients with NSCLC and PD-L1≥50% expression treated with pembrolizumab: Data from the real-life practice
Presenter: Magdalena Knetki-Wroblewska
Session: Poster session 21
1486P - Treatment patterns and real-world clinical outcomes of metastatic non-small cell lung cancer patients in the immunotherapy era
Presenter: Sarah Sharman Moser
Session: Poster session 21
1487P - Real-world efficacy and safety of anlotinib in combination with PD-1/PD-L1 inhibitors as first-line or second-line treatment in advanced non-small cell lung cancer: Updated results
Presenter: Qi-Ming Wang
Session: Poster session 21