• Dépistage, diagnostic, pronostic

  • Évaluation des technologies et des biomarqueurs

  • Voies aérodigestives supérieures

Prospective evaluation of plasma Epstein–Barr virus DNA clearance and fluorodeoxyglucose positron emission scan in assessing early response to chemotherapy in patients with advanced or recurrent nasopharyngeal carcinoma

Menée à Hong Kong sur 50 patients atteints d'un carcinome rhino-pharyngé récidivant ou de stade avancé (durée médiane de suivi : 29,1 mois), cette étude évalue l'intérêt de mesurer la clairance plasmatique de l'ADN du virus d'Epstein-Barr et de réaliser, avant puis quatre et 10 semaines après le début d'une chimiothérapie, une tomographie par émission de positrons à base de fluorodésoxyglucose pour prédire précocement la réponse thérapeutique

Background : Plasma Epstein–Barr virus (pEBV) DNA and fluorodeoxyglucose positron emission (PET) reflect tumour burden in advanced NPC. This study hypothesised that a dual endpoint based on assessing pEBV DNA clearance and PET response could predict early drug response.

Methods : Eligible patients underwent a computed tomography (CT) scan and dual PET-CT at baseline, a PET-CT at 4 weeks, and then a CT scan at 10 weeks after starting palliative or induction chemotherapy. Plasma EBV DNA clearance was determined.

Results : Fifty-eight out of 70 enrolled patients completed all imaging and 50/58 had falling pEBV DNA level, which allowed calculation of the clearance. At a median follow-up of 29.1 months, the dual endpoint (pEBV DNA clearance ≤ 10 days and > 50% drop in sum of SUVmax of target lesions) was an independent indicator of overall survival (hazard ratio (HR) = 0.135, 95% CI = 0.039 to 0.466, p = 0.0015) and progression-free survival (HR = 0.136, 95% CI = 0.048 to 0.385, p = 0002). This dual endpoint could predict subsequent response by Response Evaluation Criteria In Solid Tumours (RECIST) criteria at 10 weeks after chemotherapy.

Conclusions : Early PET-CT response and pEBV DNA clearance could predict survival and subsequent response. This dual endpoint is an innovative tool for assessing early drug response.

British Journal of Cancer , résumé, 2018

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