Follow up and late effects of childhood acute lymphoblastic leukaemia (ALL)

Your child will see their specialist doctors in clinic for at least 2 to 3 years after they have finished treatment for childhood leukaemia. After that, your child is seen in the late effects clinic. Here, they might see a doctor or an advanced nurse practitioner.

At the moment, people who have had cancer in childhood have lifelong follow up. Researchers are interested in finding out if everyone needs this level of care after childhood cancer.

At first your child usually see's their doctor every 1 to 2 months. If they are recovering well it becomes less frequent. They will have bloods and may see other members of their healthcare team in between these appointments. How often they are followed up depends on their individual needs.

At 5 years they are seen at least once a year. This might be more often depending on their individual needs. These appointments are important so even if they feel well it is important for them to go. Your child’s doctor is looking for:

  • any signs or symptoms of the leukaemia coming back

  • how they are growing and developing

  • how your child is getting on psychologically and socially after their treatment for leukaemia

  • any other problems or side effects that have come up after treatment

Together you, your child, and the treatment team can plan the best way to manage any problems if they come up.

End of treatment summary and care plan

Children and young people who have had treatment for cancer should have a care plan at the end of treatment. This plan should include:

  • their diagnosis
  • all the treatment they have had
  • possible problems they might have
  • future appointments that have been arranged
  • how any future problems should be checked out
  • who to contact with any problems

Long term side effects

Many parents worry about the possible long term effects of treatment. Some children treated for leukaemia in childhood go on to develop long term side effects. But not everyone has them. The possible long term effects depend on:

  • the type of treatment the child has had

  • the treatment dose they had

  • the age they were when they had treatment

It’s impossible to predict who will get long term side effects at the moment.

It is important to remember that the risk needs to be weighed up against the benefits of treatment. More children are surviving childhood leukaemia as treatments have improved over the last 40 to 50 years. And the risk of long term effects is also becoming less as childhood cancer treatment changes.

Possible long term late effects

Possible long term side effects include:

  • fertility Open a glossary item problems after a bone marrow or stem cell transplant
  • bone problems 
  • heart problems
  • changes in how the kidneys and heart work
  • growth problems
  • a risk of developing a second cancer

Your child’s doctor will talk to you about the possible risks depending on the treatment your child has had. They will continue to keep a close eye on your child, so that any problems can be treated early. They will work out the best way to follow them up depending on the treatment they have had.

Late effects clinic

Children who have had cancer should have follow up into adulthood.

Long term follow up clinics are available for those who are 5 years or more from the end of their cancer treatment. Your child usually sees a specialist nurse. The specialist nurse can make referrals to other professionals when needed.

Transition

Transition means moving from children’s to adult care services. It happens over a period of time and is a coordinated and planned move.

Some families worry about their child moving from children’s services into the adult services. They are sometimes concerned that the team don’t know their child well, or that adult services are busier and professionals have less time. It can also be difficult to know you're going to be less directly involved in your child’s care at this point.

Health professionals know how important this move is and there has been lots of work done in cancer services to make this move easier for everyone. Some hospitals have transition clinics to help make this as smooth as possible. It allows your older child to know what to expect and ask any questions they have.

  • European PanCareFollowUp Recommendations for surveillance of late effects of childhood, adolescent, and young adult cancer
    R J van Kalsbeek
    European Journal of Cancer, September 2021. Volume 154, Pages 316 to 328

  • Transition TYAC best practice statement for health professionals
    C Langford and others
    Teenage and Young Adults with Cancer, February 2017

  • Late Adverse Effects after Treatment for Childhood Acute Leukemia
    J Roganovic and others
    Acta Medica Academica, April 2024. Volume 53. Issue 1, Pages 59 to 80

  • Cancer in Children: Clinical Management (6th edition)
    MCG Stevens, HN Caron and A Biondi (Editors)
    Oxford University Press, 2012

  • Cancer Services for children and young people. Quality statement 6: Follow-up and monitoring of late effects
    National Institute for Health and Care Excellence (NICE), 2014

  • The information on this page is based on literature searches and specialist checking. We used many references and there are too many to list here. Please contact patientinformation@cancer.org.uk if you would like to see the full list of references we used for this information. 

Last reviewed: 
05 Dec 2024
Next review due: 
05 Dec 2027

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