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Poster Display session

499TiP - A single arm phase II trial of trastuzumab deruxtecan in patients with gastro-oesophageal adenocarcinoma cancer who are ctDNA and HER2 positive: DECIPHER (TRIALS IN PROGRESS)

Date

27 Jun 2024

Session

Poster Display session

Presenters

Elizabeth Smyth

Citation

Annals of Oncology (2024) 35 (suppl_1): S162-S204. 10.1016/annonc/annonc1482

Authors

E. Smyth1, D. Griffiths2, K. Cozens2, C. Hurt2, R. Waugh2, R. Turkington3, K. Foley4, R. Roy5, S. Sharma6, A. Jurdi7, M.C. Liu7, S. Ngan8, R. Owen9, D. Chuter2, C. Steel2, G. Griffiths2

Author affiliations

  • 1 Oxford University Hospitals NHS Foundation Trust - Churchill Hospital, Oxford/GB
  • 2 University of Southampton, Southampton/GB
  • 3 Patrick G Johnston Centre for Cancer Research - Queen's University Belfast, Belfast/GB
  • 4 Velindre Cancer Centre - Velindre NHS University Trust - NHS Wales, Cardiff/GB
  • 5 Castle Hill Hospital - Hull University Teaching Hospitals NHS Trust, Cottingham/GB
  • 6 Natera, San Carlos/US
  • 7 Natera, Inc., San Carlos/US
  • 8 Guy's and St. Thomas' Hospital NHS Trust, London/GB
  • 9 University of Oxford, Oxford/GB

Resources

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Abstract 499TiP

Background

Oesophagogastric adenocarcinoma (OGA) is globally prevalent and frequently advanced at presentation. Less than 50% of patients with operable OGA are cured when treated with multimodality therapy. Patients in the UK with operable OGA, are treated with FLOT prior to and following surgery. However, patients who have circulating tumour DNA (ctDNA) in their blood after surgery have worse survival than ctDNA negative patients. Therefore, use of novel treatment approaches aiming to cure this micrometastatic disease are considered a rational and appropriate treatment approach. Trastuzumab deruxtecan (T-DXd), a novel HER2-targeting antibody drug conjugate, is licensed to treat advanced, previously treated HER2-positive OGA. Therefore, there is a need to evaluate T-DXd in resectable HER2 and ctDNA positive OGA, where options are limited.

Trial design

Co-ordinated by the Cancer Research UK Southampton Clinical Trials Unit, DECIPHER is a single arm, multicentre, phase II trial testing the effect of T-DXd on reducing micrometastatic disease burden in HER2-positive OGA patients who are ctDNA positive after chemotherapy and surgery. To be eligible, participants must have been treated with FLOT before surgery for at least 6 weeks and must have recovered from surgery with no evidence of metastatic disease on post-surgical imaging. HER2 and ctDNA positive patients will be treated with T-DXd at a dose of 6.4 mg/kg intravenously every 21 days for a maximum of 8 cycles or until disease recurrence. If required, patients may dose reduce, but no dose re-escalation will be permitted. A clinically validated, personalised, tumour-informed ctDNA assay (signateraTM, Natera, Inc.) will be utilised to detect ctDNA in patient plasma samples. The primary endpoint is the percentage of patients who are ctDNA negative after 4 cycles of treatment. Secondary endpoints include ctDNA clearance after each cycle, disease free survival, overall survival, quality of life and frequency of adverse events. DECIPHER opened in April 2024 and will run in approximately 15 UK secondary care hospitals with the aim of recruiting 25 evaluable patients.

Clinical trial identification

NCT05965479; EudraCT 2022-003445-34; ISRCTN15960722.

Legal entity responsible for the study

University of Southampton.

Funding

AstraZeneca.

Disclosure

All authors have declared no conflicts of interest.

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