PCN42 Budget Impact Analysis of the Oncotype DX Breast Cancer Recurrence Score Test to Guide Chemotherapy Use in ER+/HER2- Node-Negative Early Invasive Breast Cancer

2021 ◽  
Vol 24 ◽  
pp. S26
Author(s):  
V. Berdunov ◽  
S. Millen ◽  
A. Paramore ◽  
S. Reynia ◽  
N. Fryer ◽  
...  
2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Mark D. Zarella ◽  
Rebecca C. Heintzelman ◽  
Nikolay K. Popnikolov ◽  
Fernando U. Garcia

2010 ◽  
Vol 134 (11) ◽  
pp. 1697-1701
Author(s):  
Jena Auerbach ◽  
Mimi Kim ◽  
Susan Fineberg

Abstract Context.—Oncotype DX is a multigene reverse transcription–polymerase chain reaction assay used to quantify recurrence risk in patients with stage I or II estrogen receptor–positive, lymph node–negative invasive breast cancer. The results are reported as a Recurrence Score (RS). The 16 cancer genes evaluated include a proliferation set, hormone receptor set, and HER2 set. The activity of these genes is addressed by pathologic assessment of breast cancers. Objective.—To determine if factors evaluated in pathologic evaluation of breast cancer could be used to predict Oncotype DX results. Design.—We studied 138 cases of invasive breast cancer for which Oncotype DX results and pathology data were available. Grading was performed by using Nottingham grading system. For hormone receptor immunostaining, 10% nuclear staining was considered a positive result. Results.—Oncotype DX RS was low in 81 cases, intermediate in 44 cases, and high in 13 cases. All 6 cases with both a negative progesterone receptor (PR) and a mitotic count score of 3 had a high RS. All 12 cases with both a negative PR and a mitotic count score greater than 1 had either an intermediate or high RS. Although Nottingham grade, PR status, mitotic count score, tumor size, and nuclear grade were each significantly associated with RS, in bivariate analyses the only variables that remained independently predictive of an intermediate or high RS score in a multivariate logistic regression model were negative PR and mitotic count score greater than 1. Conclusions.—Our study suggests that a mitotic count score greater than 1 combined with a negative PR result, as determined by pathologic assessment, could serve as a marker for an intermediate or high Oncotype DX RS.


2021 ◽  
pp. 20210348
Author(s):  
Ning Mao ◽  
Ping Yin ◽  
Haicheng Zhang ◽  
Kun Zhang ◽  
Xicheng Song ◽  
...  

Objective: This study aimed to establish a mammography-based radiomics model for predicting the risk of estrogen receptor (ER)-positive, lymph node (LN)-negative invasive breast cancer recurrence based on Oncotype DX and validated it by using multicenter data. Methods: A total of 304 potentially eligible patients with pre-operative mammography images and available Oncotype DX score were retrospectively enrolled from two hospitals. The patients were grouped as training set (168 patients), internal test set (72 patients), and external test set (64 patients). Radiomics features were extracted from the mammography images of each patient. Spearman correlation analysis, analysis of variance, and least absolute shrinkage and selection operator regression were performed to reduce the redundant features in the training set, and the least absolute shrinkage and selection operator algorithm was used to construct the radiomics signature based on selected features. Multivariate logistic regression was utilized to construct classification models that included radiomics signature and clinical risk factors to predict low vs intermediate and high recurrence risk of ER-positive, LN-negative invasive breast cancer in the training set. The models were evaluated with the receiver operating characteristic curve in the training set. The internal and external test sets were used to confirm the discriminatory power of the models. The clinical usefulness was evaluated by using decision curve analysis. Results: The radiomics signature consisting of three radiomics features achieved favorable prediction performance. The multivariate logistic regression model including radiomics signature and clinical risk factors (tumor grade and HER 2) showed good performance with areas under the curve of 0.92 (95% confidence interval [CI] 0.86 to 0.97), 0.88 (95% CI 0.75 to 1.00), and 0.84 (95% CI 0.69 to 0.99) in the training, internal and external test sets, respectively. The DCA indicated that when the threshold probability is ranges from 0.1 to 1.0, the radiomics model adds more net benefit than the “treat all” or “treat none” scheme in internal and external test sets. Conclusion: As a non-invasive pre-operative prediction tool, the mammography-based radiomics model incorporating radiomics and clinical factors show favorable predictive performance for predicting the risk of ER-positive, LN-negative invasive breast cancer recurrence based on Oncotype DX. Advances in knowledge: The mammography-based radiomics model incorporating radiomics and clinical factors shows favorable predictive performance for predicting the risk of ER-positive, LN-negative invasive breast cancer recurrence.


2011 ◽  
Vol 29 (27_suppl) ◽  
pp. 52-52
Author(s):  
K. K. L. Yap ◽  
D. N. Efiom-Ekaha

52 Background: Modified Bloom-Richardson (MBR) grade is a pathologic grading system for breast cancer that has been shown to have prognostic significance in patients with node-negative disease. Oncotype DX Score is a 21-gene expression analysis that has been clinically validated as a reliable predictor of recurrence risk for node-negative estrogen receptor-positive breast cancer. A score of less than 18 signifies a low risk of recurrence, a score of 18 to 31 signifies an intermediate risk and a score greater than 31 signifies a high risk. Several reports have questioned the concordance between the Oncotype score and MBR grade. The objective of this study is to evaluate the concordance between Oncotype score and MBR grade, thereby ascertaining if MBR is a reliable predictor of breast cancer recurrence. Methods: An IRB-exempted restrospective chart review of female patients at Wellspan Group who had Oncotype DX analysis in 2008 and 2009 was carried out. Data collected included Oncotype DX score, MBR grade, BMI and menopausal status. Data were analyzed to determine the association between Oncotype DX score and MBR grade. Results: A total of 125 patients were identified. Of these, 107 had MBR grades available. The remaining patients did not have MBR grade as it was not applicable to their breast cancer type. The mean Oncotype scores were 15.11 (95% CI 13.33-16.89) for patients with MBR grade 1 carcinoma, 20.31 (95% CI 17.90-22.72) for MBR grade 2 carcinoma, and 39.93 (95% CI 30.05-49.80) for MBR grade 3 carcinoma. The mean Oncotype score differences were 5.201 (P = .007, 95% CI 1.46-8.94) between MBR grades 1 and 2, and 19.616 (P < 0.001, 95% CI 14.14-25.09) for MBR grades 2 and 3. The ranges of Oncotype scores for MBR grade 1, grade 2 and grade 3 were 3 to 36, 9 to 56 and 20 to 70 respectively. Conclusions: MBR grade may predict breast cancer recurrence risk reliably as there is acceptable concordance between MBR grade and Oncotype Dx recurrence risk.


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