J Albanell1, A González2, M Ruiz-Borrego3, E Alba4, J A García-Saenz5, J M Corominas6, O Burgues7, V Furio8, A Rojo9, J Palacios10, B Bermejo11, M Martínez-García12, M L Limon3, A S Muñoz4, M Martín13, I Tusquets12, F Rojo14, R Colomer2, I Faull15, A Lluch11. 1. Medical Oncology Service, Hospital del Mar, Barcelona; Cancer Research Program, IMIM (Hospital del Mar Research Institute), Barcelona; Department of Medicine, Autonomous University of Barcelona, Barcelona. Electronic address: jalbanell@hospitaldelmar.cat. 2. Medical Oncology Service, MD Anderson, Madrid. 3. Medical Oncology Service, Hospital Virgen del Rocío, Sevilla. 4. Medical Oncology Service, Hospital Virgen de la Victoria, Málaga. 5. Medical Oncology Service, Hospital Clínico, Madrid. 6. Cancer Research Program, IMIM (Hospital del Mar Research Institute), Barcelona; Department of Medicine, Autonomous University of Barcelona, Barcelona; Pathology Service, Hospital del Mar, Barcelona. 7. Pathology Service, Hospital Clínico, Valencia. 8. Pathology Service, Hospital Clínico, Madrid. 9. Pathology Service, MD Anderson, Madrid. 10. Pathology Service, Hospital Virgen del Rocío, Sevilla. 11. Department of Hematology and Oncology, Hospital Clínico de Valencia, Valencia. 12. Medical Oncology Service, Hospital del Mar, Barcelona; Cancer Research Program, IMIM (Hospital del Mar Research Institute), Barcelona. 13. Medical Oncology Service, Hospital Gregorio Marañón Madrid, Madrid. 14. Cancer Research Program, IMIM (Hospital del Mar Research Institute), Barcelona; Pathology Service, Fundación Jiménez Díaz, Madrid. 15. LiveMedix, Barcelona, Spain.
Abstract
BACKGROUND: This study examined the impact of the Recurrence Score (RS) in Spanish breast cancer patients and explored the associations between clinicopathological markers and likelihood of change in treatment recommendations. PATIENTS AND METHODS: Enrollment was offered consecutively to eligible women with estrogen receptor-positive; human epidermal growth factor receptor 2-negative, node-negative breast cancer. Oncologists recorded treatment recommendation and confidence in it before and after knowing the patient's RS. RESULTS: Treatment recommendation changed in 32% of 107 patients enrolled: in 21% from chemohormonal (CHT) to hormonal therapy (HT) and in 11% from HT to CHT. RS was associated with the likelihood of change from HT to CHT (P < 0.001) and from CHT to HT (P < 0.001). Confidence of oncologists in treatment recommendations increased for 60% of cases. Higher tumor grade (P = 0.007) and a high proliferative index (Ki-67) (P = 0.023) were significantly associated with a greater chance of changing from HT to CHT, while positive progesterone receptor status (P = 0.002) with a greater probability of changing from CHT to HT. CONCLUSIONS: Results from the first prospective European study are consistent with published experience and use of the RS as proposed in European clinical practice guidelines and provide evidence on how Oncotype DX and clinicopathological factors are complementary and patient selection may be improved.
BACKGROUND: This study examined the impact of the Recurrence Score (RS) in Spanish breast cancerpatients and explored the associations between clinicopathological markers and likelihood of change in treatment recommendations. PATIENTS AND METHODS: Enrollment was offered consecutively to eligible women with estrogen receptor-positive; human epidermal growth factor receptor 2-negative, node-negative breast cancer. Oncologists recorded treatment recommendation and confidence in it before and after knowing the patient's RS. RESULTS: Treatment recommendation changed in 32% of 107 patients enrolled: in 21% from chemohormonal (CHT) to hormonal therapy (HT) and in 11% from HT to CHT. RS was associated with the likelihood of change from HT to CHT (P < 0.001) and from CHT to HT (P < 0.001). Confidence of oncologists in treatment recommendations increased for 60% of cases. Higher tumor grade (P = 0.007) and a high proliferative index (Ki-67) (P = 0.023) were significantly associated with a greater chance of changing from HT to CHT, while positive progesterone receptor status (P = 0.002) with a greater probability of changing from CHT to HT. CONCLUSIONS: Results from the first prospective European study are consistent with published experience and use of the RS as proposed in European clinical practice guidelines and provide evidence on how Oncotype DX and clinicopathological factors are complementary and patient selection may be improved.
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