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Wilms Tumor Surveillance & Follow-Up Guidelines

Young boy diagnosed with Wilms Tumor recieving chemotherapy treatment with oncologist after relapsing from stage 4 Wilms Tumor also known as nephroblastoma, childhood kidney cancer or pediatric renal cancer.

​​​What's on this page:

Learn More About Wilms Tumor Surveillance & Follow-Up After Treatment. Explore Wilms tumor (nephroblastoma) surveillance and follow-up after treatment with this evidence-based WCF educational briefing covering ongoing monitoring for children with standard- and high-risk pediatric renal tumors. Learn about the objectives of post-treatment surveillance, monitoring for possible recurrence, and the importance of structured long-term follow-up care for children and survivors of childhood kidney cancer.

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Educational Literature/ Wilms Tumor Surveillance & Follow-Up Guidelines

WCF (Briefing 6.1a -Pediatric Surveillance & Follow-up Guidelines)

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Briefing (Series 6.1a)

Surveillance & Follow-up Guidelines

Standard & High-Risk Pediatric Renal Tumor (Wilms)

This briefing provides a clear overview of post-treatment surveillance and follow-up care for pediatric renal cancer, specifically Wilms tumor. It outlines the purpose and objectives of ongoing monitoring, explains key definitions, and distinguishes between standard - and high-risk follow-up protocols. Designed to support caregivers and stakeholders, the document offers practical guidance on how long-term care is structured to detect recurrence early and ensure the best possible outcomes for children.​

Key Highlights include:​

a) Objectives of Surveillance;

b) Definitions.​

This WCF guide is for educational purposes only and is released as part of the World Health Organizations (WHO) Global initiative for Childhood Cancer (GICC). It is based on international pediatric oncology standards in Canada, the United States and Europe. Seek advice from a qualified medical professional should you have any concerns or questions. © World Health Organization (WHO). Used with permission in collaboration with the Wilms Cancer Foundation (WCF). “CureAll” is part of the WHO Global Initiative for Childhood Cancer (GICC). 

 

Available languages:


English | Français | Deutsch | Italiano | Español | Português | فارسی | العربية | हिन्दी | 中文 | 한국어

Also available via the World Health Organization (WHO) Knowledge Action Portal:

English | Français | Deutsch | Italiano | Español | Português | فارسی | العربية | हिन्दी | 中文 | 한국어

More Educational Literature in this series:

WCF (Briefing 2.1b - Wilms Cancer Foundation).png

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WCF (Briefing 2.1b - Wilms Cancer Foundation).png

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WCF (Briefing 2.2a Early Diagnosis & Long-term Outlook).png

Click to View

WCF (Briefing 2.1b - Wilms Cancer Foundation).png

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WCF (Briefing 5.7a - Pediatric Renal Cancer-Awareness-Treatment-Support).png

Click to View

WCF (Briefing 6.1a -Pediatric Surveillance & Follow-up Guidelines)

Click to View

WCF (Briefing 6.2a - Wilms Tumor Relapse).png

Click to View

What other Resources you need to know about

Advocacy Resources

Awareness Campaigns

Explore the Wilms Cancer Foundations catalog of awareness campaigns, reciprocal links and icons, etc. in support of Wilms Tumor.

Access the Wilms Cancer foundations awareness campaigns

Support Resources

Treatment Centres

Find contact information on pediatric oncology/ childhood cancer treatment centres & clinics around the world for professional support on Wlms tumor (nephroblastoma).

Access the Wilms Cancer Foundations treatment centre database

Useful Links & External Resources

Find links to third resources (support groups, imformation hubs, programs, etc) for children, parents, caregivers and healthcare professionals tackling Wilms Tumor (nephroblastoma).

Access useful links &external resources

 

Support Programs

Find support programs for children, parents, caregivers and healthcare professionals tackling Wilms Tumor (nephroblastoma).

Access support programs database

Educational Videos

Learn about Wilms Cancer Foundations educational video library in support of the WHO and Global Initiative for Childhood Cancer to support patients, parents & caregivers tackling Wilms Tumor (nephroblastoma).

Read more and gain access to educational literature (fact sheets, briefings, reports, etc.)

Patient Resources

Patient Interviews

Watch patient interviews for candid views on diagnosis, treatment, relapse, recovery, long-term effects, etc. of Wilms Tumor on the Wilms Cancer Foundations dedicated video channel.

Watch patient interviews

Patient Experiences

Hear about real patient & caregiver experiences from diagnosis, treatment, relapse, recovery and post treatment care of Wilms Tumor (nephroblastoma).

Explore patient experiences 

Patient Groups (for Children)

Active patient engagement and peer groups (Wilms Warriors) to help children connect with others with Wilms Tumor (nephroblastoma).

Access patient groups & forums for children 

Parents & Caregiver Resources

Parent Interviews

Watch parent interviews for candid views on diagnosis, treatment, relapse, recovery, long-term effects, etc. of Wilms Tumor on the Wilms Cancer Foundations dedicated video channel.

Watch parent interviews

Parent Experiences

Hear about real parent & caregiver experiences from diagnosis, treatment, relapse, recovery and post treatment care of Wilms Tumor (nephroblastoma).

Explore parent experiences

Parent Groups

WIlms Tumor online parent groups (Wilms Support Network) and forums to connect and share issues related to Wilms Tumor (nephroblastoma).

Access parent groups & forums for parent & caregivers

Parent & Caregiver Tip
Ask your child's healthcare team to explain the exact type of kidney tumor, how the diagnosis was established and which specialists will be involved in planning treatment and supporting your family.

Help Improve Outcomes for Children Worldwide

 

Support the Wilms Cancer Foundation's work in childhood cancer awareness, education, survivorship support, psychosocial care, and global advocacy. Together we can help improve access to trusted information, strengthen early diagnosis initiatives, and support children and families affected by Wilms tumor around the world.

 

For more information, guidance, and support resources please review the links provided below (and our website) or contact us directly. 

 

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