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Risk stratification in early stage luminal breast cancer patients treated with and without RT

Wadsten, Charlotta (författare)
Umeå universitet,Institutionen för kirurgisk och perioperativ vetenskap
Whitworth, Pat W. (författare)
Patel, Rakesh (författare)
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Savala, Jess (författare)
Warnberg, Fredrik (författare)
Bremer, Troy (författare)
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 (creator_code:org_t)
Umea Univ, Dept Surg & Perioperat Sci, Umea, Sweden. Nashville Breast Ctr, Nashville, TN USA. Univ WI Hosp, Madison, WI USA. PreludeDx, Laguna Hills, CA USA. Uppsala Univ, Reg Oncol Ctr, Uppsala, Sweden. American Society of Clinical Oncology, 2019
2019
Engelska.
Ingår i: Journal of Clinical Oncology. - Umea Univ, Dept Surg & Perioperat Sci, Umea, Sweden. Nashville Breast Ctr, Nashville, TN USA. Univ WI Hosp, Madison, WI USA. PreludeDx, Laguna Hills, CA USA. Uppsala Univ, Reg Oncol Ctr, Uppsala, Sweden. : American Society of Clinical Oncology. - 0732-183X .- 1527-7755. ; 37:15, s. 568-568
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
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  • Background: The goal was to develop and validate a biologic signature for 10-year ipsilateral invasive breast event (IBE) risk in luminal Stage 1 breast cancer (BC) patients treated surgically and either with or without radiation therapy (RT). Methods: This cohort was from Uppsala University and Västerås Hospitals diagnosed with Stage 1 BC and treated surgically between 1987 and 2004. Treatment was neither randomized nor strictly rules based, including adjuvant RT, Hormone Therapy (HT), and Chemotherapy (CT). Biomarkers (HER2, PR, Ki67, COX2, p16/INK4A, FOXA1 and SIAH2) were assessed on tissue microarrays in PreludeDx’s CLIA lab by board-certified pathologists. Risk groups were calculated using biomarkers and clinical factors age and size. A multivariate Cox proportional hazards analysis was used to determine hazard ratio for biologic signature. 10-year IBE risk was assessed using Kaplan-Meier survival analysis. Results: There were 423 luminal cases with biomarker data having 54 IBEs, and a median follow-up of 11.8 years. There were 372 patients treated with BCS and 51 with Mastectomy, and 325 received RT, 169 received HT, and 47 received CT. In a multivariate analysis, the biologic signature (HR = 1.6, p = 0.019) and RT (HR = 0.51, p = 0.027) were associated with IBE risk adjusting for other treatments (HT and CT) and Luminal A status (p = 0.37). For patients over 50 yrs of age with luminal A disease and treated without CT (n = 205), an elevated biologic signature identified a subset of patients with a 15% (+/- 14%) 10-year IBE risk without RT (n = 38) compared to a 4% (+/-6%) IBE risk with RT (n = 72), while patients with a low biologic signature had a 10-year IBE risk of 4% (+/- 4%) without RT (n = 26) and 3% (+/-5%) IBE risk with RT (n = 69). Conclusions: With further prospective validation, the biologic signature identified herein may provide a tool enabling improved management for women diagnosed with early luminal BC.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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