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Skjemafor minimetodevurdering vurderingavnyemetoderisykehus Versjon2.0/10.2013 Tittel: Dato: Helseforetak: AnsvarligFagperson: Bibliotekar: konom: Fagfelle:Genomtest(OncotypeDX)forutvalgtebrystkreftpasienter
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How to fill out genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter
01
Obtain a tissue sample from the breast cancer patient.
02
Send the tissue sample to a laboratory that offers the Oncotype DX test for breast cancer.
03
The laboratory will analyze the tissue sample to determine the patient's Oncotype DX score.
04
Review the results of the test with the patient's healthcare provider to determine the appropriate treatment plan.
Who needs genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter?
01
Patients with early-stage, hormone receptor-positive, HER2-negative breast cancer may benefit from the Oncotype DX test to help guide treatment decisions.
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What is genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter?
Genomtest Oncotype DX is a genomic test used to analyze the expression of specific genes in breast cancer patients to help predict the likelihood of cancer recurrence and to assist in treatment decisions.
Who is required to file genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter?
Healthcare providers and oncologists who are managing breast cancer patients eligible for genomic testing are required to file the test.
How to fill out genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter?
Filling out the test involves providing patient demographic information, clinical details including tumor characteristics, and selecting the appropriate gene panel based on the patient's specific circumstances.
What is the purpose of genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter?
The purpose of the test is to provide information about the aggressiveness of the breast cancer and inform decisions regarding chemotherapy treatment options.
What information must be reported on genomtest-oncotype-dx-for-utvalgte-brystkreftpasienter?
Information that must be reported includes patient ID, tumor pathology report, clinical history, and results of the genomic analysis.
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