Resumen
Purpose: Increased vascularity is a hallmark of renal cell carcinoma (RCC). Microvessel density (MVD) is one measurement of tumor angiogenesis; however, its utility as a biomarker of outcome is unknown. ECOG-ACRIN 2805 (E2805) enrolled 1,943 resected high-risk RCC patients randomized to adjuvant sunitinib, sorafenib, or placebo. We aimed to determine the prognostic and predictive role of MVD in RCC. Experimental Design: We obtained pretreatment primary RCC nephrectomy tissues from 822 patients on E2805 and constructed tissue microarrays. Using quantitative immunofluorescence, we measured tumor MVD as the area of CD34- expressing cells. We determined the association with diseasefree survival (DFS), overall survival (OS), treatment arm, and clinicopathologic variables. Results: High MVD (above the median) was associated with prolonged OS for the entire cohort (P = 0.021) and for patients treated with placebo (P = 0.028). The association between high MVD and OS was weaker in patients treated with sunitinib or sorafenib (P = 0.060). MVD was not associated with DFS (P = 1.00). On multivariable analysis, MVD remained independently associated with improved OS (P = 0.013). High MVD correlated with Fuhrman grade 1-2 (P < 0.001), clear cell histology (P < 0.001), and absence of necrosis (P < 0.001) but not with gender, age, sarcomatoid features, lymphovascular invasion, or tumor size. Conclusions: High MVD in resected high-risk RCC patients is an independent prognostic, rather than predictive, biomarker of improved OS. Further studies should assess whether incorporating MVD into clinical models will enhance our ability to predict outcome and if low MVD can be used for selection of high-risk patients for adjuvant therapy trials.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 217-223 |
| Número de páginas | 7 |
| Publicación | Clinical Cancer Research |
| Volumen | 24 |
| N.º | 1 |
| DOI | |
| Estado | Published - ene 1 2018 |
Nota bibliográfica
Publisher Copyright:© 2018 American Association for Cancer Research.
Financiación
This work was supported by CA180820, CA180794, CA180826, and in part by NIH grants R-01 CA158167 and K24 CA172123 (to H.M. Kluger, principal investigator). L.B. Jilaveanu is also supported by the Lung Cancer Research Foundation-LUNGevity and Melanoma Research Alliance Award #308721.
| Financiadores | Número del financiador |
|---|---|
| Lung Cancer Research Foundation-LUNGevity | |
| National Institutes of Health (NIH) | K24 CA172123 |
| National Institutes of Health (NIH) | |
| National Childhood Cancer Registry – National Cancer Institute | R01CA158167 |
| National Childhood Cancer Registry – National Cancer Institute | |
| Melanoma Research Alliance Foundation | 308721 |
| Melanoma Research Alliance Foundation | |
| Lung Cancer Research Foundation |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- General Medicine
Huella
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