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Liver Directed Therapy for Renal Cell Carcinoma

Background: Metastatic renal cell carcinoma (RCC) to the liver portrays a poor prognosis and liver directed therapy remains controversial. We aimed to determine potential selection criteria for patients who might benefit from this strategy. Materials and Methods: We evaluated 247 consecutive patient...

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Autores principales: Langan, Russell C., Ripley, R. Taylor, Davis, Jeremy L., Prieto, Peter A., Datrice, Nicole, Steinberg, Seth M., Bratslavsky, Gennady, Rudloff, Udo, Kammula, Udai S., Stojadinovic, Alexander, Avital, Itzhak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342526/
https://www.ncbi.nlm.nih.gov/pubmed/22558019
http://dx.doi.org/10.7150/jca.4456
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author Langan, Russell C.
Ripley, R. Taylor
Davis, Jeremy L.
Prieto, Peter A.
Datrice, Nicole
Steinberg, Seth M.
Bratslavsky, Gennady
Rudloff, Udo
Kammula, Udai S.
Stojadinovic, Alexander
Avital, Itzhak
author_facet Langan, Russell C.
Ripley, R. Taylor
Davis, Jeremy L.
Prieto, Peter A.
Datrice, Nicole
Steinberg, Seth M.
Bratslavsky, Gennady
Rudloff, Udo
Kammula, Udai S.
Stojadinovic, Alexander
Avital, Itzhak
author_sort Langan, Russell C.
collection PubMed
description Background: Metastatic renal cell carcinoma (RCC) to the liver portrays a poor prognosis and liver directed therapy remains controversial. We aimed to determine potential selection criteria for patients who might benefit from this strategy. Materials and Methods: We evaluated 247 consecutive patients with RCC metastatic to the liver from a prospectively maintained database. Results: Eighteen patients received liver directed therapy (18/247, 7%). Ten patients underwent liver resection (10/247, 4%) and eight patients underwent radiofrequency ablation (RFA, 8/247, 3%). All were rendered free of disease in the liver. Five had synchronous liver disease and underwent synchronous resections with their primary. Mortality was 0%. Fourteen had single (surgery 7, RFA 7) and four (surgery 3, RFA 1) had multiple liver lesions, respectively. Median size of lesions was 5cm (0.5 - 10cm) and 2.5cm (1 - 6cm) in the surgery and RFA groups, respectively. Median DFI was 10 months, and no difference was observed in those with a longer vs. shorter than median DFI (p = 0.95); liver specific progression free survival for the surgery and RFA groups were 4 and 6 months, respectively (p= 0.93). 1, 3 and 5-year actuarial survivals for the whole group were 89%, 40%, 27%. Median survival for the surgery group was 24 (3 to 254+) months, and for the RFA group 15.6 (7-56+) months (p = 0.56). Metachronous liver disease was associated with prolonged survival (p = 0.02). Conclusions: Liver directed therapy for RCC is safe. For highly selected patients with metachronous liver RCC metastases, liver directed therapy should be considered in a multidisciplinary manner.
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spelling pubmed-33425262012-05-03 Liver Directed Therapy for Renal Cell Carcinoma Langan, Russell C. Ripley, R. Taylor Davis, Jeremy L. Prieto, Peter A. Datrice, Nicole Steinberg, Seth M. Bratslavsky, Gennady Rudloff, Udo Kammula, Udai S. Stojadinovic, Alexander Avital, Itzhak J Cancer Research Paper Background: Metastatic renal cell carcinoma (RCC) to the liver portrays a poor prognosis and liver directed therapy remains controversial. We aimed to determine potential selection criteria for patients who might benefit from this strategy. Materials and Methods: We evaluated 247 consecutive patients with RCC metastatic to the liver from a prospectively maintained database. Results: Eighteen patients received liver directed therapy (18/247, 7%). Ten patients underwent liver resection (10/247, 4%) and eight patients underwent radiofrequency ablation (RFA, 8/247, 3%). All were rendered free of disease in the liver. Five had synchronous liver disease and underwent synchronous resections with their primary. Mortality was 0%. Fourteen had single (surgery 7, RFA 7) and four (surgery 3, RFA 1) had multiple liver lesions, respectively. Median size of lesions was 5cm (0.5 - 10cm) and 2.5cm (1 - 6cm) in the surgery and RFA groups, respectively. Median DFI was 10 months, and no difference was observed in those with a longer vs. shorter than median DFI (p = 0.95); liver specific progression free survival for the surgery and RFA groups were 4 and 6 months, respectively (p= 0.93). 1, 3 and 5-year actuarial survivals for the whole group were 89%, 40%, 27%. Median survival for the surgery group was 24 (3 to 254+) months, and for the RFA group 15.6 (7-56+) months (p = 0.56). Metachronous liver disease was associated with prolonged survival (p = 0.02). Conclusions: Liver directed therapy for RCC is safe. For highly selected patients with metachronous liver RCC metastases, liver directed therapy should be considered in a multidisciplinary manner. Ivyspring International Publisher 2012-04-20 /pmc/articles/PMC3342526/ /pubmed/22558019 http://dx.doi.org/10.7150/jca.4456 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Langan, Russell C.
Ripley, R. Taylor
Davis, Jeremy L.
Prieto, Peter A.
Datrice, Nicole
Steinberg, Seth M.
Bratslavsky, Gennady
Rudloff, Udo
Kammula, Udai S.
Stojadinovic, Alexander
Avital, Itzhak
Liver Directed Therapy for Renal Cell Carcinoma
title Liver Directed Therapy for Renal Cell Carcinoma
title_full Liver Directed Therapy for Renal Cell Carcinoma
title_fullStr Liver Directed Therapy for Renal Cell Carcinoma
title_full_unstemmed Liver Directed Therapy for Renal Cell Carcinoma
title_short Liver Directed Therapy for Renal Cell Carcinoma
title_sort liver directed therapy for renal cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342526/
https://www.ncbi.nlm.nih.gov/pubmed/22558019
http://dx.doi.org/10.7150/jca.4456
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