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The growth rate of “clinically significant” renal cancer

Surveillance studies of enhancing renal masses report on a mean tumor growth rate of about 0.3 cm/year. In most of these studies however, only small tumors in elderly patients were followed. In the current report, we attempt to evaluate the growth rate of “clinically significant” renal carcinomas de...

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Autores principales: Gofrit, Ofer N., Yutkin, Vladimir, Zorn, Kevin C., Duvdevani, Mordechai, Landau, Ezekiel H., Hidas, Guy, Pode, Dov
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628034/
https://www.ncbi.nlm.nih.gov/pubmed/26543715
http://dx.doi.org/10.1186/s40064-015-1385-9
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author Gofrit, Ofer N.
Yutkin, Vladimir
Zorn, Kevin C.
Duvdevani, Mordechai
Landau, Ezekiel H.
Hidas, Guy
Pode, Dov
author_facet Gofrit, Ofer N.
Yutkin, Vladimir
Zorn, Kevin C.
Duvdevani, Mordechai
Landau, Ezekiel H.
Hidas, Guy
Pode, Dov
author_sort Gofrit, Ofer N.
collection PubMed
description Surveillance studies of enhancing renal masses report on a mean tumor growth rate of about 0.3 cm/year. In most of these studies however, only small tumors in elderly patients were followed. In the current report, we attempt to evaluate the growth rate of “clinically significant” renal carcinomas defined as tumors that were treated immediately upon diagnosis. 46 patients (mean age 64 years SD 11 years) were treated for renal carcinoma. All had a cross-sectional imaging studies performed 6–60 months prior to diagnosis of kidney cancer demonstrating no tumor. Tumor growth rate was calculated by dividing tumor’s largest diameter by the time interval between the normal kidney imaging and diagnosis of renal cancer. Mean tumor diameter was 4.5 cm (SD 2.4 cm). Mean time period from the normal imaging to diagnosis of renal cancer was 33.6 months (SD 18 months). According to the proposed model, the average growth rate of “clinically significant” renal carcinomas was 2.13 cm/year (SD 1.45, range 0.2–6.5 cm/year). Tumor growth rate correlated inversely with patient’s age (p = 0.007). Patient gender or Fuhrman’s grade did not correlate however. The growth rate of “clinically significant” renal cancer appears to be higher than the rate reported in surveillance trials. Renal tumors tend to grow faster in young patients. As such, variable growth rate should be taken into account when considering active surveillance in young patients and when designing trials for evaluation of anti-cancer agents.
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spelling pubmed-46280342015-11-05 The growth rate of “clinically significant” renal cancer Gofrit, Ofer N. Yutkin, Vladimir Zorn, Kevin C. Duvdevani, Mordechai Landau, Ezekiel H. Hidas, Guy Pode, Dov Springerplus Research Surveillance studies of enhancing renal masses report on a mean tumor growth rate of about 0.3 cm/year. In most of these studies however, only small tumors in elderly patients were followed. In the current report, we attempt to evaluate the growth rate of “clinically significant” renal carcinomas defined as tumors that were treated immediately upon diagnosis. 46 patients (mean age 64 years SD 11 years) were treated for renal carcinoma. All had a cross-sectional imaging studies performed 6–60 months prior to diagnosis of kidney cancer demonstrating no tumor. Tumor growth rate was calculated by dividing tumor’s largest diameter by the time interval between the normal kidney imaging and diagnosis of renal cancer. Mean tumor diameter was 4.5 cm (SD 2.4 cm). Mean time period from the normal imaging to diagnosis of renal cancer was 33.6 months (SD 18 months). According to the proposed model, the average growth rate of “clinically significant” renal carcinomas was 2.13 cm/year (SD 1.45, range 0.2–6.5 cm/year). Tumor growth rate correlated inversely with patient’s age (p = 0.007). Patient gender or Fuhrman’s grade did not correlate however. The growth rate of “clinically significant” renal cancer appears to be higher than the rate reported in surveillance trials. Renal tumors tend to grow faster in young patients. As such, variable growth rate should be taken into account when considering active surveillance in young patients and when designing trials for evaluation of anti-cancer agents. Springer International Publishing 2015-10-06 /pmc/articles/PMC4628034/ /pubmed/26543715 http://dx.doi.org/10.1186/s40064-015-1385-9 Text en © Gofrit et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Gofrit, Ofer N.
Yutkin, Vladimir
Zorn, Kevin C.
Duvdevani, Mordechai
Landau, Ezekiel H.
Hidas, Guy
Pode, Dov
The growth rate of “clinically significant” renal cancer
title The growth rate of “clinically significant” renal cancer
title_full The growth rate of “clinically significant” renal cancer
title_fullStr The growth rate of “clinically significant” renal cancer
title_full_unstemmed The growth rate of “clinically significant” renal cancer
title_short The growth rate of “clinically significant” renal cancer
title_sort growth rate of “clinically significant” renal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628034/
https://www.ncbi.nlm.nih.gov/pubmed/26543715
http://dx.doi.org/10.1186/s40064-015-1385-9
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