¿Son todos los test genómicos iguales?

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“Tratamiento médico del cáncer en el año 2019”
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NH Collection Eurobuilding
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C O O R D I N A D O R E S C I E N T Í F I C O S :
Eduardo Díaz-Rubio
Enrique Aranda Aguilar
Enrique Grande Pulido
Ana Lluch Hernández
Pedro Pérez Segura
Mariano Provencio Pulla
¿Son todos los test genómicos iguales?:
95% CI, 9.3%-25.3%) and the RS (19.4%; 95% CI, 12.5%-
29.5%) (Figure 1 and Table 2).
Good risk stratification in this pati
served for the BCI, ROR, and EPclin (Figure
ROR categorized 15 women (9.7%) into th
Table 3. Univariate HRs and C Indexes for All Prognostic Signatures According to Nodal Status
During Years 5 to 10
Gene
Signature
Patient Group
ase
(n = 535)
Node-Positive Disease
(n = 154)
HR (95% CI)a C Index (95% CI) HR (95% CI)a C Index (95% CI)
CTS 1.95 (1.43-2.65) 0.721 (0.654-0.788) 1.61 (1.05-2.47) 0.644 (0.534-0.753)
IHC4 1.59 (1.16-2.16) 0.660 (0.576-0.745) 1.20 (0.79-1.81) 0.579 (0.460-0.697)
RS 1.46 (1.09-1.96) 0.585 (0.467-0.702) 1.24 (0.81-1.90) 0.555 (0.418-0.693)
BCI 2.30 (1.61-3.30) 0.749 (0.668-0.830) 1.60 (1.04-2.47) 0.633 (0.514-0.751)
ROR 2.77 (1.93-3.96) 0.789 (0.724-0.854) 1.65 (1.08-2.51) 0.643 (0.528-0.758)
EPclin 2.19 (1.62-2.97) 0.768 (0.701-0.835) 1.87 (1.27-2.76) 0.697 (0.594-0.799)
Abbreviation
Index; CTS, C
EPclin, Endo
HR, hazard r
immunohist
ROR, risk of r
RS, recurren
a All HRs indi
Research Original Investigation Prognostic Signatures for Estrogen Recept
Comparison of the Performance of 6 Prognostic Signatures
for Estrogen Receptor–Positive Breast Cancer
A Secondary Analysis of a Randomized Clinical Trial
IvanaSestak,PhD;RichardBuus,PhD;JackCuzick,PhD;Pet rDubsky,MD;RalfKronenwett,MD;
CarstenDenkert,MD;SeanFerree,PhD;DennisSgroi,MD;CatherineSchnabel,PhD;
FrederickL.Baehner,MD;ElizabethMallon,PhD;MitchDowsett,PhD
IMPORTANCE Multiple molecular signatures are available for managing estrogen receptor
(ER)–positive breast cancer but with little direct comparative information to guide the
patient’s choice.
OBJECTIVE To conduct a within-patient comparison of the prognostic value of 6 multigene
signatures in women with early ER-positive breast cancer who received endocrine therapy for
5 years.
DESIGN, SETTING, AND PARTICIPANTS This retrospective biomarker analysis included 774
postmenopausal women with ER-positive ERBB2 (formerly HER2)–negative breast cancer.
Anastrozole or
ent with
anastrozole vs tamoxifen with 10-year follow-up data. The signatures included the Oncotype
Dx recurr ce scor k of recurrence (ROR), Breast Cancer Index
(BCI), EndoPredict (EPclin), Clinical Treatment Score, and 4-marker immunohistochemical
score. Data were collected from January 2009, through April 2015.
MAIN OU COMES AND MEASURES The primary objective was to compare the prognostic value
of these signatures in addition to the Clinical Treatment Score (nodal status, tumor size,
grade, age, and endocrine treatment) for distant recurrence for 0 to 10 years and 5 to 10
years after diagnosis. Likelihood ratio (LR) statistics were used with the χ2 test and C indexes
to assess the prognostic value of each signature.
RESULTS In this study of 774 postmenopausal women with ER-positive,ERBB2 -negative
disease (mean [SD] age, 64.1 [8.1] years), 591 (mean [SD] age, 63.4 [7.9] years) had
node-negative disease. The signatures providing the most prognostic information were the
ROR (hazard ratio [HR], 2.56; 95% CI, 1.96-3.35), followed by the BCI (HR, 2.46; 95% CI,
1.88-3.23) and EPclin (HR, 2.14; 95% CI, 1.71-2.68). Each provided significantly more
information than the Clinical Treatment Score (HR, 1.99; 95% CI, 1.58-2.50), the recurrence
score (HR, 1.69; 95% CI, 1.40-2.03), and the 4-marker immunohistochemical score (HR, 1.95;
95% CI, 1.55-2.45). Substantially less information was provided by all 6 molecular tests for the
183 patients with 1 to 3 positive nodes, but the BCI (ΔLR χ2= 9.2) and EPclin (ΔLR χ2 = 7.4)
provided more additional prognostic information than the other signatures.
CONCLUSIONS AND RELEVANCE For women with node-negative disease, the ROR, BCI, and
EPclin were significantly more prognostic for overall and late distant recurrence. For women
with 1 to 3 positive nodes, limited independent information was available from any test.
These data might help oncologists and patients to choose the most appropriate test when
considering chemotherapy use and/or extended endocrine therapy.
TRIAL REGISTRATION Identifier: ISRCTN18233230
Supplementalcontent
AuthorAffiliations: Author
affiliationsarelistedattheendofthis
article.
CorrespondingAuthor: Ivana
Research
JAMA Oncology | Original Investigation