Wilms' tumor and neuroblastoma
Authors:
BZ Morgenstern a;
AP Krivoshik a;
V. Rodriguez a;
PM Anderson a
| Affiliation: | a Department of Pediatric and Adolescent Medicine, Mayo Medical School and Mayo Clinic, Rochester, Minnesota, USA |
DOI:
10.1080/08035320310021336
Publication Frequency:
12 issues per year
Subject:
Pediatrics & Child Health;
Number of References: 35
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The circumstances under which this title is published have changed:
Reason for change: Changed Publisher
Now published by: Blackwell
Date of change: 31 December 2006
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Abstract
Significant differences exist between the European and North American treatment protocols for Wilms' tumor and neuroblastoma. There are variations in biopsy technique, timing and extent of initial surgery, chemotherapy protocols and dosage routines, as well as the type of salvage therapy. With the consolidation of the two major North American study groups into a single entity (Children's Oncology Group), the European and North American study groups represent the only remaining large-scale venues for treatment comparison. It is important to study and understand the variation in treatment protocols in order to maintain an open forum of scientific investigation that will lead to improving the care and outcome of children with cancer. It is anticipated that the unification of the North American groups will lead to greater interest and scientific cooperation with the European study group. This paper will serve as a forum for such a discussion at a local level.
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| Keywords: Neuroblastoma; treatment; Wilms' tumor |
| view references (35) |

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