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Topotecan distribution in an anephric infant with therapy resistant bilateral Wilms tumor with a novel germline WT1 gene mutation

Authors :
Lugtenberg, R.T. (Rieneke)
Cransberg, K. (Karlien)
Loos, W.J. (Walter)
Wagner, A. (Anja)
Alders, M. (Mariëlle)
Heuvel-Eibrink, M.M. (Marry) van den
Lugtenberg, R.T. (Rieneke)
Cransberg, K. (Karlien)
Loos, W.J. (Walter)
Wagner, A. (Anja)
Alders, M. (Mariëlle)
Heuvel-Eibrink, M.M. (Marry) van den
Publication Year :
2008

Abstract

The therapeutic strategy for bilateral Wilms tumor (WT) remains a challenge. Especially in cases with chemotherapy resistant disease, bilateral nephrectomy is sometimes inevitable. For optimal cure rates stage V WT patients benefit from adjuvant treatment; however, there are limited data available on chemotherapy pharmacokinetics in anephric children. In this report, we describe a 10-month old girl with bilateral Wilms tumor and a novel germline WT1 gene mutation. This patient hardly showed any response on preoperative chemotherapy, and ultimately, underwent sequential bilateral tumor-nephrectomy. Subsequently, during peritoneal dialysis, she received topotecan as adjuvant chemotherapy based on plasma levels, indicating that this is a reasonable option as adjuvant treatment in therapy-resistant Wilms tumor patients after bilateral nephrectomy. This case showed a novel germline WT1 gene mutation of which the correlation with resistant phenotype has to be confirmed in larger cohorts of WT patients.

Details

Database :
OAIster
Notes :
application/pdf, Cancer Chemotherapy and Pharmacology vol. 62 no. 6, pp. 1039-1044, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn957099105
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1007.s00280-008-0694-x