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. 2014 Jun 17;9(3):154–160. doi: 10.1159/000363755

Table 2.

Commercially available molecular tests

Mammaprint™ Oncotype DXTM EndoPredict™ ProsignaTM
Provider Agendia Genomic Health Sividon NanoString
Type of assay 70-gene assay 21-gene RS 11-gene assay 50-gene assay
Type of tissue fresh frozen FFPE FFPE FFPE
Technique DNA microarrays qRT-PCR qRT-PCR qRT-PCR
Central laboratory yes yes no no
Indication and population studied prognostic, N0–1 prognostic, N0–1 ER+ prognostic, N0–1 ER+/HER2− prognostic, N0–1
Analytical validation yes yes yes yes
Clinical validation yes yes yes yes
Prospective-retrospective evidence observational feasibility NSABP B-14 (14%), ABCSG 6 (19%), MA.12 (49%),
(% of recruited patients) study (RASTER) (73%) NSABP B-20 (28%), ABCSG 8 (36%), MA.5 (66%),
SWOG 8814 (40%), GEICAM/9906 (64%) ABCSG 8 (40%),
ATAC (30%) ATAC (16%),
GEICAM/9906 (66%)
Prospective evidence (pending) MINDACT TAILORX, RxPONDER, ADAPT
CTS C B B B
LoE2009 II I I I
AGO recommendation +/− +a +a +/−

AGO = Arbeitsgemeinschaft für Gynäkologische Onkologie, CTS = category of tumor marker studies, ER = estrogen receptor, FFPE = formalin-fixed paraffin-embedded, HER2 = human epidermal growth factor receptor 2, LoE = level of evidence, qRT-PCR = quantitative reverse transcription-polymerase chain reaction, RS = recurrence score.

a

Should only be used in selected node-negative patients if all other criteria are inconclusive for therapeutic decision-making.