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This document is a consent form that allows for the disclosure of a child's medical information to facilitate research into the causes and factors associated with Wilms tumor.
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How to fill out North American Wilms Tumor Study, NAWTS

01
Obtain the NAWTS data collection forms from the official NAWTS website or coordinating center.
02
Carefully read the instructions provided for each section of the form to understand the required information.
03
Gather all necessary patient medical records and relevant data needed to complete the forms accurately.
04
Fill out patient demographic information, including age, gender, and diagnosis date.
05
Document the clinical details carefully, including treatment protocols, outcomes, and any adverse events.
06
Review the collected data for completeness and accuracy before final submission.
07
Submit the completed forms through the designated submission channel as instructed in the guidelines.

Who needs North American Wilms Tumor Study, NAWTS?

01
Pediatric oncologists and healthcare professionals managing patients diagnosed with Wilms tumor.
02
Researchers studying Wilms tumor for clinical trials, epidemiological studies, or treatment protocols.
03
Institutions involved in pediatric cancer treatment and research requiring standardized data collection.
04
Patients and families seeking access to new treatment options or clinical trials through the study.
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MD Anderson's Children's Cancer Hospital is one of the nation's foremost treatment and research facilities for Wilms' tumors. When your child is a patient here, we customize a plan of action that includes the most advanced therapies with the least impact on the body.
With marked improvements in chemotherapy, the overwhelming majority of affected children now survive. Overall 5-year survival in the US is 92% but in poor parts of the world with fewer resources, the survival rate is only 78%. Wilms tumor is associated with a number of specific syndromes including WAGR syndrome.
MD Anderson's Children's Cancer Hospital is one of the nation's foremost treatment and research facilities for Wilms' tumors. When your child is a patient here, we customize a plan of action that includes the most advanced therapies with the least impact on the body.
With marked improvements in chemotherapy, the overwhelming majority of affected children now survive. Overall 5-year survival in the US is 92% but in poor parts of the world with fewer resources, the survival rate is only 78%. Wilms tumor is associated with a number of specific syndromes including WAGR syndrome.
Wilms tumour classically follows the “rule of 10's”: up to 10% may have unfavourable histology, 10% are bilateral, 10% have vascular invasion, 10% have calcifications on CT and 10% have pulmonary metastases at presentation [19].
The National Wilms Tumor Study Group (NWTS) is a cancer research cooperative group in the United States formed to study a type of kidney tumor that affects children called Wilms' tumor. In 2001, NWTS merged with several other pediatric oncology cooperative groups to create the Children's Oncology Group (COG).
Wilms tumor is a rare kidney cancer that mainly affects children. Also known as nephroblastoma, it's the most common cancer of the kidneys in children.
The Treatment of Wilms Tumor: Results of the National Wilms Tumor Studies. The survival expectancy for Wilms tumor patients has increased dramatically from about 50% at the beginning of the National Wilms Tumor Study (NWTS) trials to a current expectancy in the 90% range.

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The North American Wilms Tumor Study (NAWTS) is a collaborative research initiative focused on understanding and improving treatment for Wilms tumor, which is a type of kidney cancer that primarily affects children.
Participants in the North American Wilms Tumor Study, such as healthcare professionals, researchers, and institutions involved in the treatment or study of Wilms tumor, are required to file NAWTS.
To fill out the NAWTS, participants should follow the specific guidelines provided in the study protocol, ensuring that all required fields are completed accurately and any necessary documentation is attached.
The purpose of NAWTS is to collect and analyze data on Wilms tumor cases to enhance treatment protocols, improve survival rates, and understand the disease better through collaborative research.
The information that must be reported includes patient demographics, clinical data, treatment protocols, outcomes, and any adverse events related to treatment, as outlined in the study's data collection forms.
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