Multigene Signature Result
Notes
**Note 1:** Physician statement of the Multigene Signature Results can be used to code this data item.
**Note 2:** Multigene signatures or classifiers are assays of a panel of genes from a tumor specimen, intended to provide a quantitative assessment of the likelihood of response to chemotherapy and to evaluate prognosis or the likelihood of future metastasis.
* Only record tests done on tumor tissue that help determine if the cancer is likely to recur. Don’t include other tests, such as those that evaluate hereditary mutations that influence a patient’s risk of developing cancer (e.g. myRisk, BRCA)
* Only record tests that are based on gene assays. Don’t include other tests which use a multivariate data model to eliminate the need for genetic assays
**Note 3:** Code the score or risk for the test performed. The same test should be used to record information in 3894: Multigene Signature Method.
**Note 4:** Oncotype Dx tests are not recorded in this data item. See the following data items for Oncotype Dx.
* 3903: Oncotype Dx Recurrence Score-DCIS
* 3904: Oncotype Dx Recurrence Score-Invasive
* 3905: Oncotype Dx Risk Level-DCIS
* 3906: Oncotype Dx Risk Level-Invasive
**Note 5:** PAM50 (Prosigna) is a single numeric score of 0-100. If the score is available, record the score. If only the risk level is available, record that.
**Note 6:** For Mammaprint, EndoPredict, and Breast Cancer Index, only record the risk level.
Default
X8
Metadata
SSDI
| Code |
Description |
| 00-99 |
Enter actual recurrence score
Note: Depending on the test, the range of values may be different |
| X1 |
Score 100 |
| X2 |
Low risk |
| X3 |
Moderate [intermediate] risk |
| X4 |
High risk |
| X7 |
Test done, results not in chart |
| X8 |
Not applicable: Information not collected for this case
(If this item is required by your standard setter, use of code X8 will result in an edit error.) |
| X9 |
Not documented in medical record
Multigene Signature Results not assessed or unknown if assessed |
