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Comparison of a gene expression profiling strategy to standard clinical work-up for determination of tumour origin in cancer of unknown primary (CUP)

par Ades Moraes, Felipe ;de Azambuja, Evandro ;Daugaard, Gedske;Ameye, Lieveke;Moulin Correa, Camilo ;Paesmans, Marianne ;De Jong, Daphne;Decoster, Lore;De Greve, Jacques;Ismael, Gustavo ;Møller, Anne Kirstine;Piccart-Gebhart, Martine ;Awada, Ahmad
Référence Journal of chemotherapy, 25, 4, page (239-246)
Publication Publié, 2013-08

Article révisé par les pairs

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Résumé :

CupPrint® is a genomic signature able to identify 47 different cancer types. The aim of our study was to compare the accuracy of this genomic signature to that of a full clinical work-up in diagnosing the primary tumour site. Patients with newly diagnosed, untreated metastatic tumours were eligible for this trial. The clinical work-up and gene expression profiling on a biopsy from a metastatic site were started at the same time. The study was planned using a one-stage Fleming design. Patients in whom no primary site was diagnosed by the clinical work-up were excluded. Out of the 67 patients registered, the primary site was identified by clinical work-up in 36 patients, and diagnosis with CupPrint was obtained in 53. There were 31 evaluable patients with both clinical and CupPrint diagnoses, and out of these a similar diagnosis was obtained in 11 patients, i.e. the concordance rate was 35% (95% confidence interval: 19-55%). The median time to diagnosis through the clinical work-up was 48 days, and 10 days with CupPrint (P<0.001). We concluded that in patients with newly diagnosed metastatic tumours, CupPrint has low accuracy in diagnosing the primary cancer site. © 2013 Edizioni Scientifiche per l'Informazione su Farmaci e Terapia.