TY - JOUR
T1 - Oncotype DXA® in breast cancer patients
T2 - clinical experience, outcome and follow-up-a case-control study
AU - Rath, Michelle G.
AU - Uhlmann, Lorenz
AU - Fiedler, Marita
AU - Heil, Joerg
AU - Golatta, Michael
AU - Dinkic, Christine
AU - Hennigs, Andre
AU - Schott, Sarah
AU - Ernst, Veronika
AU - Koch, Thorsten
AU - Sohn, Christof
AU - Brucker, Cosima
AU - Rom, Joachim
N1 - Rath, Fiedler, Ernst, Koch, Brucker: Department of Gynecology and Obstetrics, Paracelsus Medical University, Nuremberg, Germany
PY - 2018/2
Y1 - 2018/2
N2 - Breast cancer is the leading cause of death from cancer in women and the most common cancer in the world [1]. To date, many patients with estrogen-receptor-positive (ER+) breast cancer are overtreated with chemotherapy when the rationale for adjuvant chemotherapy is based on clinicopathologic parameters. Different studies were able to demonstrate that a 21-gene expression assay (Oncotype DXA (R) Genomic Health, Redwood City, CA) can predict the benefit from adjuvant chemotherapy in ER+ breast cancers [2, 3] and provide additional prognostic information independent of clinicopathological features [4].Data from all patients with ER+ Her2neu- breast cancer undergoing Oncotype DXA (R) testing between 2011 and 2014 at a tertiary referral center in Germany were analyzed. Oncotype DXA (R) was performed in 69 cases, in 2 cases data were missing and in 3 cases Oncotype DXA (R) could not be performed by the company. The results showed a low risk in 39 cases, an intermediate risk in 22 cases and a high risk in 3 cases. Based on Oncotype results, treatment recommendations were changed in 39 of 64 patients (61%). Before Oncotype DXA (R) testing, chemotherapy was recommended in 67 patients, afterwards only in 25 patients. Data from 44 of 67 patients were matched to controls for stage, tumor grade, menopausal and hormone receptor status. Within a mean observation time of 19.7 months, cancer recurrence was observed in two patients.Oncotype DXA (R) testing can be recommended for risk-tailored chemotherapy. Results should be validated in larger prospective studies.
AB - Breast cancer is the leading cause of death from cancer in women and the most common cancer in the world [1]. To date, many patients with estrogen-receptor-positive (ER+) breast cancer are overtreated with chemotherapy when the rationale for adjuvant chemotherapy is based on clinicopathologic parameters. Different studies were able to demonstrate that a 21-gene expression assay (Oncotype DXA (R) Genomic Health, Redwood City, CA) can predict the benefit from adjuvant chemotherapy in ER+ breast cancers [2, 3] and provide additional prognostic information independent of clinicopathological features [4].Data from all patients with ER+ Her2neu- breast cancer undergoing Oncotype DXA (R) testing between 2011 and 2014 at a tertiary referral center in Germany were analyzed. Oncotype DXA (R) was performed in 69 cases, in 2 cases data were missing and in 3 cases Oncotype DXA (R) could not be performed by the company. The results showed a low risk in 39 cases, an intermediate risk in 22 cases and a high risk in 3 cases. Based on Oncotype results, treatment recommendations were changed in 39 of 64 patients (61%). Before Oncotype DXA (R) testing, chemotherapy was recommended in 67 patients, afterwards only in 25 patients. Data from 44 of 67 patients were matched to controls for stage, tumor grade, menopausal and hormone receptor status. Within a mean observation time of 19.7 months, cancer recurrence was observed in two patients.Oncotype DXA (R) testing can be recommended for risk-tailored chemotherapy. Results should be validated in larger prospective studies.
KW - Breast cancer
KW - Case-control study
KW - Gene expression assay
KW - Oncotype DX (R)
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pmu_pure&SrcAuth=WosAPI&KeyUT=WOS:000423102400022&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1007/s00404-017-4618-z
DO - 10.1007/s00404-017-4618-z
M3 - Original Article
C2 - 29236174
SN - 0932-0067
VL - 297
SP - 443
EP - 447
JO - ARCHIVES OF GYNECOLOGY AND OBSTETRICS
JF - ARCHIVES OF GYNECOLOGY AND OBSTETRICS
IS - 2
ER -