Skip to main content
Top
Published in: Familial Cancer 2/2012

01-06-2012 | Original Article

Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months

Authors: Jin Zhang, Jia-Hua Pan, Bai-Jun Dong, Wei Xue, Dong-ming Liu, Yi-Ran Huang

Published in: Familial Cancer | Issue 2/2012

Login to get access

Abstract

To evaluate the natural outcome of a surveillance strategy for enhancing renal masses associated with von Hippel-Lindau disease (VHL). From January 1988 to June 2011, a watchful waiting strategy was carried out in 16 cases with 42 enhancing renal masses. Clinical data were reviewed to determine tumor growth rate, subsequent interventions, and outcome of follow-up. During a median follow-up of 83 months (range, 55–279), 18 surgical interventions were performed in 13 cases; local recurrence of tumor occurred in 4 cases; 4 patients died (two of metastasis disease, one of CNS Hemangioblastomas with hemorrhage, and one of an unrelated disease) and 12 survived. The median follow-up duration for 42 renal masses was 56 months (range, 19–116 months). The mean tumor growth rate observed was 0.529 cm/year (range, 0.036–1.870 cm/year). The mean growth rate of the tumors larger than 3 cm was 0.573 cm/year, which was not significantly different from that of those smaller tumors (growth rate 0.507 cm/year, P = 0.5905). There was no significant correlation between initial tumor size and growth rate in our cohort with a correlation coefficient of 0.149(P = 0.3480). At the last follow-up, 38 (90.5%) tumors were larger than 3 cm and no metastasis disease developed among tumors ≤4 cm. Progression to metastatic disease was detected in 2 patients. The majority of the enhancing renal masses with VHL disease may still be indolent and do not metastasize during a long period of follow-up even in tumors larger than 3 cm. Metastatic potential during active surveillance appears to be low in VHL patients with Renal tumors ≤4 cm.
Literature
1.
go back to reference Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA (1990) Clinical features and natural history of von Hippel-Lindau disease. Q J Med 77:1151–1163PubMedCrossRef Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA (1990) Clinical features and natural history of von Hippel-Lindau disease. Q J Med 77:1151–1163PubMedCrossRef
2.
go back to reference Lonser RR, Glenn GM, Walther M, Chew EY, Libutti SK, Linehan WM, Oldfield EH (2003) Von Hippel-Lindau disease. Lancet 361:2059–2067PubMedCrossRef Lonser RR, Glenn GM, Walther M, Chew EY, Libutti SK, Linehan WM, Oldfield EH (2003) Von Hippel-Lindau disease. Lancet 361:2059–2067PubMedCrossRef
3.
go back to reference Latif F, Tory K, Gnarra J et al (1993) Identification of the von Hippel–Lindau disease tumor suppressor gene. Science 260:1317–1320PubMedCrossRef Latif F, Tory K, Gnarra J et al (1993) Identification of the von Hippel–Lindau disease tumor suppressor gene. Science 260:1317–1320PubMedCrossRef
4.
go back to reference Grubb RL III, Choyke PL, Pinto PA, Linehan WM, Walther MM (2005) Management of von Hippel-Lindau associated kidney cancer. Nat Clin Pract Urol 2:248–255PubMedCrossRef Grubb RL III, Choyke PL, Pinto PA, Linehan WM, Walther MM (2005) Management of von Hippel-Lindau associated kidney cancer. Nat Clin Pract Urol 2:248–255PubMedCrossRef
5.
go back to reference Bratslavsky G, Liu JJ, Johnson AD et al (2008) Salvage partial nephrectomy for hereditary renal cancer: feasibility and outcomes. J Urol 179:67–70PubMedCrossRef Bratslavsky G, Liu JJ, Johnson AD et al (2008) Salvage partial nephrectomy for hereditary renal cancer: feasibility and outcomes. J Urol 179:67–70PubMedCrossRef
6.
go back to reference Joly D, Méjean A, Corréas JM et al (2011) Progress in nephron sparing therapy for renal cell carcinoma and von Hippel-Lindau disease. J Urol 185:2056–2060PubMedCrossRef Joly D, Méjean A, Corréas JM et al (2011) Progress in nephron sparing therapy for renal cell carcinoma and von Hippel-Lindau disease. J Urol 185:2056–2060PubMedCrossRef
7.
go back to reference Walther MM, Choyke PL, Glenn G, Lyne JC, Rayford W, Venzon D, Linehan WM (1999) Renal cancer in families with hereditary renal cancer: prospective analysis of a tumor size threshold for renal parenchymal sparing surgery. J Urol 161:1475–1479PubMedCrossRef Walther MM, Choyke PL, Glenn G, Lyne JC, Rayford W, Venzon D, Linehan WM (1999) Renal cancer in families with hereditary renal cancer: prospective analysis of a tumor size threshold for renal parenchymal sparing surgery. J Urol 161:1475–1479PubMedCrossRef
8.
go back to reference Duffey BG, Choyke PL, Glenn G, Grubb RL, Venzon D, Linehan WM, Walther MM (2004) The relationship between renal tumor size and metatases in patients with von Hippel-Lindau disease. J Urol 172:63–65PubMedCrossRef Duffey BG, Choyke PL, Glenn G, Grubb RL, Venzon D, Linehan WM, Walther MM (2004) The relationship between renal tumor size and metatases in patients with von Hippel-Lindau disease. J Urol 172:63–65PubMedCrossRef
9.
go back to reference Ploussard G, Droupy S, Ferlicot S, Ples R, Rocher L, Richard S, Benoit G (2007) Local recurrence after nephron-sparing surgery in von Hippel-Lindau disease. Urology 70:435–439PubMedCrossRef Ploussard G, Droupy S, Ferlicot S, Ples R, Rocher L, Richard S, Benoit G (2007) Local recurrence after nephron-sparing surgery in von Hippel-Lindau disease. Urology 70:435–439PubMedCrossRef
10.
go back to reference Matin SF, Ahrar K, Wood CG, Daniels M, Jonasch E (2008) Patterns of intervention for renal lesions in von Hippel-Lindau disease. BJU 102:940–945CrossRef Matin SF, Ahrar K, Wood CG, Daniels M, Jonasch E (2008) Patterns of intervention for renal lesions in von Hippel-Lindau disease. BJU 102:940–945CrossRef
11.
go back to reference Maher ER, Yates JR, Harries R et al (1990) Clinical features and natural history of von Hippel-Lindau disease. Q J Med 77:1151–1163PubMedCrossRef Maher ER, Yates JR, Harries R et al (1990) Clinical features and natural history of von Hippel-Lindau disease. Q J Med 77:1151–1163PubMedCrossRef
12.
go back to reference Matthews JN, Altman DG, Campbell MJ, Royston P (1990) Analysis of serial measurements in medical research. BMJ 300:230–235PubMedCrossRef Matthews JN, Altman DG, Campbell MJ, Royston P (1990) Analysis of serial measurements in medical research. BMJ 300:230–235PubMedCrossRef
13.
go back to reference Zhang J, Huang Y, Pan J et al (2008) Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families. J Cancer Res Clin Oncol 134:1211–1218PubMedCrossRef Zhang J, Huang Y, Pan J et al (2008) Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families. J Cancer Res Clin Oncol 134:1211–1218PubMedCrossRef
14.
go back to reference Choyke PL, Walther MM, Zbar B et al (1992) The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patients. AJR Am J Roentgenol 159:1229–1234PubMed Choyke PL, Walther MM, Zbar B et al (1992) The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patients. AJR Am J Roentgenol 159:1229–1234PubMed
15.
go back to reference Neumann HP, Bender BU, Berger DP et al (1998) Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma. J Urol 160:1248–1254PubMedCrossRef Neumann HP, Bender BU, Berger DP et al (1998) Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma. J Urol 160:1248–1254PubMedCrossRef
16.
go back to reference Gupta GN, Peterson J, Thakore KN, Pinto PA, Linehan WM, Bratslavsky G (2010) Oncological outcomes of partial nephrectomy for multifocal renal cell carcinoma greater than 4 cm. J Urol 184:59–63PubMedCrossRef Gupta GN, Peterson J, Thakore KN, Pinto PA, Linehan WM, Bratslavsky G (2010) Oncological outcomes of partial nephrectomy for multifocal renal cell carcinoma greater than 4 cm. J Urol 184:59–63PubMedCrossRef
17.
go back to reference Steinbach F, Novick AC, Zincke H et al (1995) Treatment of renal cell carcinoma in von Hippel-Lindau disease: a multicenter study. J Urol 153:1812–1816PubMedCrossRef Steinbach F, Novick AC, Zincke H et al (1995) Treatment of renal cell carcinoma in von Hippel-Lindau disease: a multicenter study. J Urol 153:1812–1816PubMedCrossRef
18.
go back to reference Chawla SN, Crispen PL, Hanlon AL, Greenberg RE, Chen DY, Uzzo RG (2006) The natural history of observed enhancing renal masses: meta-analysis and review of the world literature. J Urol 175:425–431PubMedCrossRef Chawla SN, Crispen PL, Hanlon AL, Greenberg RE, Chen DY, Uzzo RG (2006) The natural history of observed enhancing renal masses: meta-analysis and review of the world literature. J Urol 175:425–431PubMedCrossRef
19.
go back to reference Kouba E, Smith A, McRackan D, Wallen EM, Pruthi RS (2007) Watchful waiting for solid renal masses: insight into the natural history and results of delayed intervention. J Urol 177:466–470PubMedCrossRef Kouba E, Smith A, McRackan D, Wallen EM, Pruthi RS (2007) Watchful waiting for solid renal masses: insight into the natural history and results of delayed intervention. J Urol 177:466–470PubMedCrossRef
20.
go back to reference Abouassaly R, Lane BR, Novick AC (2008) Active surveillance of renal masses in elderly patients. J Urol 180:505–509PubMedCrossRef Abouassaly R, Lane BR, Novick AC (2008) Active surveillance of renal masses in elderly patients. J Urol 180:505–509PubMedCrossRef
21.
go back to reference Beisland C, Hjelle KM, Reisæter LAR, Bostad L (2009) Observation should be considered as an alternative in management of renal masses in older and comorbid patients. E Urol 55:1419–1429CrossRef Beisland C, Hjelle KM, Reisæter LAR, Bostad L (2009) Observation should be considered as an alternative in management of renal masses in older and comorbid patients. E Urol 55:1419–1429CrossRef
22.
go back to reference Abou YT, Kassouf W, Steinberg J, Aprikian AG, Laplante MP, Tanguay S (2007) Active surveillance for selected patients with renal masses: updated results with long-term follow-up. Cancer 110:1010–1014CrossRef Abou YT, Kassouf W, Steinberg J, Aprikian AG, Laplante MP, Tanguay S (2007) Active surveillance for selected patients with renal masses: updated results with long-term follow-up. Cancer 110:1010–1014CrossRef
23.
go back to reference Rosales JC, Haramis G, Moreno J, Badani K, Benson MC, McKiernan J, Casazza C, Landman J (2010) Active surveillance for renal cortical neoplasms. J Urol 183:1698–1702PubMedCrossRef Rosales JC, Haramis G, Moreno J, Badani K, Benson MC, McKiernan J, Casazza C, Landman J (2010) Active surveillance for renal cortical neoplasms. J Urol 183:1698–1702PubMedCrossRef
24.
go back to reference Campbell SC, Novick AC, Belldegrun A et al (2009) Guideline for management of the clinical T1 renal mass. J Urol 182:1271–1279PubMedCrossRef Campbell SC, Novick AC, Belldegrun A et al (2009) Guideline for management of the clinical T1 renal mass. J Urol 182:1271–1279PubMedCrossRef
Metadata
Title
Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months
Authors
Jin Zhang
Jia-Hua Pan
Bai-Jun Dong
Wei Xue
Dong-ming Liu
Yi-Ran Huang
Publication date
01-06-2012
Publisher
Springer Netherlands
Published in
Familial Cancer / Issue 2/2012
Print ISSN: 1389-9600
Electronic ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-011-9503-5

Other articles of this Issue 2/2012

Familial Cancer 2/2012 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine