Your browser doesn't support javascript.
Results of the c-TRAK TN trial: a clinical trial utilising ctDNA mutation tracking to detect molecular residual disease and trigger intervention in patients with moderate and high-risk early stage triple negative breast cancer.
Turner, Nicholas C; Swift, Claire; Jenkins, Ben; Kilburn, Lucy; Coakley, Maria; Beaney, Matthew; Fox, Lisa; Goddard, Katie; Garcia-Murillas, Isaac; Proszek, Paula; Hall, Peter; Wynne, Catherine Harper; Hickish, Tamas; Kernaghan, Sarah; Macpherson, Iain R; Okines, Alicia; Palmieri, Carlo; Perry, Sophie; Randle, Katrina; Snowdon, Claire; Stobart, Hilary; Wardley, Andrew; Wheatley, Duncan; Waters, Simon; Winter, Matthew; Hubank, Michael; Allen, Steven; Bliss, Judith M.
  • Turner NC; Breast Cancer Now Research Centre, The Institute of Cancer Research, London, UK; Breast Unit, The Royal Marsden Hospital, London, UK.
  • Swift C; The Institute of Cancer Research, London, UK; The Royal Marsden NHS Foundation Trust.
  • Jenkins B; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Kilburn L; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Coakley M; The Institute of Cancer Research, London, UK; The Royal Marsden NHS Foundation Trust.
  • Beaney M; The Institute of Cancer Research, London, UK.
  • Fox L; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Goddard K; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Garcia-Murillas I; The Institute of Cancer Research, London, UK.
  • Proszek P; NIHR Centre for Molecular Pathology, Royal Marsden Hospital, London, UK.
  • Hall P; University of Edinburgh, Edinburgh, UK.
  • Wynne CH; Maidstone Hospital, Maidstone and Tunbridge Wells NHS Trust, Maidstone, UK.
  • Hickish T; University Hospitals Dorset NHS Foundation Trust, Bournemouth, UK.
  • Kernaghan S; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Macpherson IR; The Beatson West of Scotland Cancer Centre, Glasgow, UK.
  • Okines A; Breast Unit, The Royal Marsden Hospital, London, UK.
  • Palmieri C; Clatterbridge Cancer Centre NHS Trust.
  • Perry S; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Randle K; Independent Cancer Patients' Voice, London, UK.
  • Snowdon C; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
  • Stobart H; Independent Cancer Patients' Voice, London, UK.
  • Wardley A; Outreach Research & Innovation Group Ltd, Manchester, UK.
  • Wheatley D; Royal Cornwall Hospitals NHS Trust, Truro, UK.
  • Waters S; Velindre Cancer Centre, Velindre University NHS Trust, Cardiff, UK.
  • Winter M; Weston Park Hospital; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield UK.
  • Hubank M; The Institute of Cancer Research, London, UK; The Royal Marsden NHS Foundation Trust.
  • Allen S; The Royal Marsden NHS Foundation Trust.
  • Bliss JM; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
Ann Oncol ; 2022 Nov 21.
Artículo en Inglés | MEDLINE | ID: covidwho-2236452
ABSTRACT

BACKGROUND:

Post-treatment detection of circulating tumour DNA (ctDNA) in early-stage triple negative breast cancer (TNBC) patients predicts high risk of relapse. c-TRAK-TN assessed the utility of prospective ctDNA surveillance in TNBC and the activity of pembrolizumab in patients with ctDNA detected (ctDNA+). PATIENTS AND

METHODS:

c-TRAK-TN, a multi-centre phase II trial, with integrated prospective ctDNA surveillance by digital PCR, enrolled patients with early-stage TNBC and residual disease following neoadjuvant chemotherapy, or, stage II/III with adjuvant chemotherapy. ctDNA surveillance comprised three monthly blood sampling to 12 months (18 months if samples were missed due to COVID), and ctDNA+ patients were randomised 21; interventionobservation. ctDNA results were blinded unless patients were allocated to intervention, when staging scans were done and those free of recurrence were offered pembrolizumab. A protocol amendment (16/09/2020) closed the observation group; all subsequent ctDNA+ patients were allocated to intervention. Co-primary endpoints were i) ctDNA detection rate ii) sustained ctDNA clearance rate on pembrolizumab (NCT03145961).

RESULTS:

208 patients registered between 30/01/18 - 06/12/19, 185 had tumour sequenced, 171 (92·4%) had trackable mutations, and 161 entered ctDNA surveillance. Rate of ctDNA detection by 12 months was 27·3% (44/161,95%CI20·6-34·9). Seven patients relapsed without prior ctDNA detection. 45 patients entered the therapeutic component (intervention n=31; observation n=14; 1 observation patient was re-allocated to intervention following protocol amendment). Of patients allocated intervention, 72% (23/32) had metastases on staging at time of ctDNA+, and 4 patients declined pembrolizumab. Of the five patients who commenced pembrolizumab, none achieved sustained ctDNA clearance.

CONCLUSION:

c-TRAK-TN is the first prospective study to assess whether ctDNA assays have clinical utility in guiding therapy in TNBC. Patients had a high rate of metastatic disease on ctDNA detection. Findings have implications for future trial design, emphasising the importance of commencing ctDNA testing early, with more sensitive and/or frequent ctDNA testing regimes.
Palabras clave

Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Tipo de estudio: Estudio de cohorte / Estudios diagnósticos / Estudio experimental / Estudio observacional / Estudio pronóstico / Ensayo controlado aleatorizado Idioma: Inglés Asunto de la revista: Neoplasmas Año: 2022 Tipo del documento: Artículo País de afiliación: J.annonc.2022.11.005

Similares

MEDLINE

...
LILACS

LIS


Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Tipo de estudio: Estudio de cohorte / Estudios diagnósticos / Estudio experimental / Estudio observacional / Estudio pronóstico / Ensayo controlado aleatorizado Idioma: Inglés Asunto de la revista: Neoplasmas Año: 2022 Tipo del documento: Artículo País de afiliación: J.annonc.2022.11.005