What if my child can’t have surgery for neuroblastoma?
Clinical decisions about whether your child can have surgery are based on individual risk factors and your child’s specific case.
Sometimes, the sequence of treatments may differ from the usual approach. In some cases, it may not be possible to surgically remove the primary tumour after induction chemotherapy has been used to shrink it. If this happens, your child may need further chemotherapy or other treatments.
Your medical team will carefully monitor your child’s response to each stage of treatment and will discuss the next steps with you at every point. If surgery isn’t possible, your child’s team will consider other options and tailor the treatment plan to their needs.
If you are unsure about the treatment plan, you may wish to seek a second opinion. This can be done via the National Neuroblastoma Advisory Panel, which brings together leading clinicians from across the UK who specialise in neuroblastoma treatment.
The panel holds regular meetings where individual cases are presented anonymously, alongside relevant scans and tumour genetic information. Each case is thoroughly reviewed, allowing experts to share their knowledge and recommend the most appropriate treatment plan for your child. You can ask your child’s consultant to be referred to this panel.
Find out more about the National Neuroblastoma Advisory Panel.
Support for your family
Our Family Support Team is here to help if you need impartial guidance or simply want to talk things through.
Other questions you may have
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What is the National Neuroblastoma Advisory Panel?
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What is the treatment for high-risk neuroblastoma?
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What is the treatment for intermediate-risk neuroblastoma?
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What is the treatment for low-risk neuroblastoma?
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Can I get a second opinion about my child’s diagnosis or treatment plan?
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Should I tell my consultant that I want a second opinion?
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