Oncotype DX Predictive Nomogram for Recurrence Score Output: The Novel System ADAPTED01 Based on Quantitative Immunochemistry Analysis.
Adult
Aged
Aged, 80 and over
Biomarkers, Tumor
/ genetics
Breast Neoplasms
/ genetics
Estrogen Receptor alpha
/ metabolism
Female
Gene Expression Profiling
/ methods
Genetic Testing
/ economics
Humans
Immunohistochemistry
/ economics
Ki-67 Antigen
/ metabolism
Middle Aged
Neoplasm Recurrence, Local
/ genetics
Nomograms
Prognosis
ROC Curve
Receptors, Progesterone
/ metabolism
Retrospective Studies
Adjuvant chemotherapy
Breast cancer
Decision supporting system
Health costs
Quantitative IHC
Journal
Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
11
12
2019
revised:
21
04
2020
accepted:
23
04
2020
pubmed:
23
6
2020
medline:
3
11
2021
entrez:
23
6
2020
Statut:
ppublish
Résumé
Oncotype DX (ODX) predicts breast cancer recurrence risk, guiding the choice of adjuvant treatment. In many countries, access to the test is not always available. We used correlation between phenotypical tumor characteristics, quantitative classical immunohistochemistry (IHC), and recurrence score (RS) assessed by ODX to develop a decision supporting system for clinical use. Breast cancer patients who underwent ODX testing between 2014 and 2018 were retrospectively included in the study. The data selected for analysis were age, menopausal status, and pathologic and IHC features. IHC was performed with standardized quantitative methods. The data set was split into two subsets: 70% for the training set and 30% for the internal validation set. Statistically significant features were included in logistic models to predict RS ≤ 25 or ≤ 20. Another set was used for external validation to test reproducibility of prediction models. The internal set included 407 patients. Mean (range) age was 53.7 (31-80) years, and 222 patients (54.55%) were > 50 years old. ODX results showed 67 patients (16.6%) had RS between 0 and 10, 272 patients between 11 and 25 (66.8%), and 68 patients > 26 (16.6%). Logistic regression analysis showed that RS score (for threshold ≤ 25) was significantly associated with estrogen receptor (P = .004), progesterone receptor (P < .0001), and Ki-67 (P < .0001). Generalized linear regression resulted in a model that had an area under the receiver operating characteristic curve (AUC) of 92.2 (sensitivity 84.2%, specificity 80.1%) and that was well calibrated. The external validation set (183 patients) analysis confirmed the model performance, with an AUC of 82.3 and a positive predictive value of 91%. A nomogram was generated for further prospective evaluation to predict RS ≤ 25. RS was related to quantitative IHC in patients with RS ≤ 25, with a good performance of the statistical model in both internal and external validation. A nomogram for enhancing clinical approach in a cost-effective manner was developed. Prospective studies must test this application in clinical practice.
Identifiants
pubmed: 32565110
pii: S1526-8209(20)30090-2
doi: 10.1016/j.clbc.2020.04.012
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
ESR1 protein, human
0
Estrogen Receptor alpha
0
Ki-67 Antigen
0
MKI67 protein, human
0
Receptors, Progesterone
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e600-e611Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.