2016
DOI: 10.1158/1538-7445.sabcs15-p5-08-02
|View full text |Cite
|
Sign up to set email alerts
|

Abstract P5-08-02: Real-life analysis evaluating 1594 N0/Nmic breast cancer patients for whom treatment decisions incorporated the 21-gene recurrence score result: 5-year KM estimate for breast cancer specific survival with recurrence score results ≤30 is >98%

Abstract: Background: The 21-Gene Recurrence Score® Assay (Oncotype DX®) has been validated as a prognostic and predictive tool in estrogen receptor (ER)+ breast cancer in multiple studies using archival specimens of clinical trials with long term follow up. Prospective outcome data from patients where treatment decisions incorporated the Recurrence Score results have not been reported. We evaluated treatments and clinical outcomes in patients undergoing Recurrence Score testing in 9 medical centers within Clalit Health… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
27
0
2

Year Published

2016
2016
2020
2020

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 20 publications
(31 citation statements)
references
References 0 publications
2
27
0
2
Order By: Relevance
“…The analyses used conventional AJCC T, N, and M categories as well as tumor grade and ER, PR, and Table 9 summarizes 5-year outcome data from studies using multigene panels to define low-risk patients who were treated predominantly without systemic chemotherapy. [16][17][18][19]21 For such low-risk patients, downstaging to stage I based on biology is supported by the consistently low 5-year risk of recurrence. The major impact of a multigene panel in the eighth edition prognostic stage grouping is the downstaging of biologically low-risk T2 N0 from stage II to stage I for tumors with a low Oncotype DX recurrence score.…”
Section: M0 Includes M0 With Isolated Tumor Cells (I1)mentioning
confidence: 99%
“…The analyses used conventional AJCC T, N, and M categories as well as tumor grade and ER, PR, and Table 9 summarizes 5-year outcome data from studies using multigene panels to define low-risk patients who were treated predominantly without systemic chemotherapy. [16][17][18][19]21 For such low-risk patients, downstaging to stage I based on biology is supported by the consistently low 5-year risk of recurrence. The major impact of a multigene panel in the eighth edition prognostic stage grouping is the downstaging of biologically low-risk T2 N0 from stage II to stage I for tumors with a low Oncotype DX recurrence score.…”
Section: M0 Includes M0 With Isolated Tumor Cells (I1)mentioning
confidence: 99%
“…However, these data suggest that physicians in the Breast DX study were probably reluctant to avoid CT for patients with RS values falling in the “gray area” of 11–17. Other studies reported lower rates of CT+HT use in case of RS 18–25, but these cohorts included almost exclusively patients with node‐negative or N1mi cancer .…”
Section: Discussionmentioning
confidence: 98%
“…Clinical and pathological characteristics, treatment and outcome were retrieved from medical files of the 27 BRCA carriers treated at Hadassah Medical Center and compared with a cohort of 1594 Israeli patients which was recently published …”
Section: Methodsmentioning
confidence: 99%