Educational content from recorded physician discussions — not medical advice. Talk to your (or your child's) care team about your situation.
Video
Updated Favorable histology Wilms tumor risk stratification: Rationale for future Children’s Oncology Group clinical trials
53 s · Published Apr 2026
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Social Determinants of Health Influence on Survival in Wilms Tumor, Neuroblastoma, and Hepatoblastoma
1 min · Published Jan 2026
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Wilms Tumor Rapid Fire: Update Course 2015
8 min · Published Nov 2015
Video
Impact of Pulmonary Tumor Burden in Favorable Histology Wilms Tumor Outcomes: A Report From the Children's Oncology Group Study AREN053
1 min · Published Mar 2026
Podcast
Topics in 10: Wilms Tumor
12 min · Published Aug 2019
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Journal of Pediatric Surgery Article Highlights: April 2022
8 min · Published Jul 2022
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Clinical & Research Update: Renal Tumors with Drs. Ethan Smith, Lindsay Haacker, Michael Daugherty, and Meera Kotagal
71 min · Published Sep 2026
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Clinical & Research Update: Neuroblastoma with Drs. Katherine Somers, Cara Morin, Juan Gurria, and Meera Kotagal
67 min · Published Sep 2026
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Clinical & Research Update: Sarcoma w/ Drs. Roshni Dasgupta, Joseph Pressey, Arthur Meyer, Luke Pater
66 min · Published Sep 2026
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Update Course Rewind 2025: Nerve Monitoring in Pediatric Thyroid Surgery
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Journal of Pediatric Surgery Article Review: June 2023, AAP Issue
Todd Ponsky · 13 min · Published Jul 2026
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Pediatric Surgical Oncology Research Collaborative (PSORC): Studying Rare Pediatric Tumors
56 s · Published May 2026
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Intestinal Atresia Types Explained: Grossfeld Classification for Pediatric Surgery
1 min · Published Sep 2026
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Derivation and validation of the Pediatric Community-Acquired Pneumonia Severity (PedCAPS) score: A prospective cohort study
50 s · Published Sep 2026
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FETO for Late-Diagnosed Severe Congenital Diaphragmatic Hernia (CDH) at Cincinnati Children's with Dr. Beth Rymeski
4 min · Published Sep 2026
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Severe Congenital Diaphragmatic Hernia (CDH) Case: FETO Management & Unexpected Findings with Dr. Beth Rymeski
3 min · Published Sep 2026
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Fetoscopic Endoluminal Tracheal Occlusion (FETO) Procedure: Step-by-Step Guide with Dr. Beth Rymeski
4 min · Published Sep 2026
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Choledochal Cyst Types Explained: Pediatric Surgery Fundamentals
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What the experts said
European colleagues following SIOP guidelines would offer chemotherapy without biopsy for Wilms tumor.
At COG (Children's Oncology Group) sites in North America, the approach would be resection and diagnosis.
Doxorubicin would be added to chemotherapy even for a low stage tumor under certain conditions.
Doxorubicin is added when there is loss of heterozygosity at 1P and 16Q.
Loss of heterozygosity at 1P and 16Q shows higher recurrence in Wilms tumor.
For surgeons, there will be more waiting for the biology results before determining if chemotherapy is needed, affecting decisions about port placement.
It is not accurate to tell patients that if they are less than 2 years of age and the tumor is less than 550g, they will not need chemotherapy, because biology studies may require adding chemotherapy.
Chemotherapy must be added if there is loss of heterozygosity at 1P and 16Q.
Even in stage 1 favorable histology, chemotherapy is still added if there is loss of heterozygosity at 1P and 16Q.
Loss of heterozygosity is the loss of genetic diversity in tumor cells and can indicate more aggressive disease in Wilms tumor.
Gain of 1Q refers to an extra copy of a section of chromosome 1, which is linked to worse outcomes in some cancers.
According to Children's Oncology Group updates, adverse biologic factors are associated with worse prognosis in stage 2 patients, but not in stage 1 favorable histology Wilms tumor patients.
The North American COG approach often involves immediate surgery, while the European SIOP approach typically starts with chemotherapy before surgery.
Genetic markers like loss of heterozygosity at specific chromosomes can indicate a higher risk of cancer recurrence and guide decisions about adding chemotherapy treatments.
