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Our 24/7 cancer helpline provides information and answers for people dealing with cancer. We can connect you with trained cancer information specialists who will answer questions about a cancer diagnosis and provide guidance and a compassionate ear.
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Our highly trained specialists are available 24/7 via phone and on weekdays can assist through online chat. We connect patients, caregivers, and family members with essential services and resources at every step of their cancer journey. Ask us how you can get involved and support the fight against cancer. Some of the topics we can assist with include:
For medical questions, we encourage you to review our information with your doctor.
If your child has been diagnosed with leukemia, the cancer care team will discuss treatment options with you. It is important to weigh the benefits of each treatment option against the possible risks and side effects.
The main treatments for most childhood leukemias are medications like chemotherapy, immunotherapy, and targeted drugs. For some children with higher-risk leukemias or leukemias that have not responded well to treatment, high-dose chemotherapy may be given along with a stem cell transplant. Other treatments may be used in special circumstances.
After leukemia is diagnosed and tests have been done to determine the specific type, your child’s cancer care team will discuss the treatment options with you. The most important factor in choosing a treatment is the type of leukemia, but other factors also play a role.
Treatment of acute forms of childhood leukemia (ALL or AML) is usually very intensive, so it is important that it take place in a center that specializes in treating childhood cancers.
Children and teens with leukemia and their families have special needs that can best be met by children’s cancer centers. These centers have teams of specialists who know the differences between cancers in adults and those in children and teens, as well as the unique needs of younger people with cancer.
For childhood leukemias, this team is typically led by a pediatric oncologist, a doctor who treats cancer in children. Many other health professionals may be involved in your child’s care as well, including other doctors, nurses, nurse practitioners (NPs), physician assistants (PAs), psychologists, social workers, dieticians, rehabilitation specialists, and others.
After leukemia is diagnosed and tests have been done to determine its type, your child’s cancer care team will discuss the treatment options with you.
It is important to discuss your child’s treatment options as well as their possible side effects with the treatment team to help make the decision that is the best fit for your child. If there is anything you do not understand, ask to have it explained.
Learn more in Talking to Your Child’s Cancer Care Team.
Choosing a treatment
What to expect during treatment
Possible side effects and long-term effects
Support and resources
Before treatment, the doctors and other members of the team will help you understand the tests that will need to be done.
Your child’s cancer care team will also often include a social worker. The team’s social worker will be there to support you and your family before, during and after treatment. Adjusting to a new cancer diagnosis and its treatment plan can be tough, but the cancer care team is there to help. Learn more in Helping Your Child Adjust to a Cancer Diagnosis.
Social and emotional distress may come up during and after treatment. Factors such as the child’s age and the extent of treatment can play a role.
Some children have emotional or psychological health issues that need to be addressed during and after treatment. Depending on their age, they may also have some problems with normal functioning and schoolwork. These types of issues can often be helped with support and encouragement. Doctors and other members of the health care team can also often recommend special support programs and services to help children after treatment. For more information, see Helping Your Child Transition from Treatment to Survivorship.
Many experts recommend that school-aged patients attend school as much as they can. This can help them maintain a routine and tell their friends about what is happening.
Friends can be a great source of support, but patients and parents should know that some people may have wrong ideas about cancer and fears of their own. Some cancer centers have school re-entry programs that can help in these situations. In these programs, health educators visit the school and tell students about cancer, its treatment and what changes they may notice in their classmate. They also answer any questions their class might have. (For more information, see Going to School During and After Cancer Treatment.)
Parents and other family members can also be affected, both emotionally and in other ways. Some common family concerns during treatment include financial stresses, traveling to and staying near the cancer center, the need to take time off from work, and the need for home schooling. Social workers and others at your treatment center can help sort through these issues.
Centers that treat many patients with leukemia may have programs to introduce new patients and their families to others who have finished their treatment. This can give them an idea of what to expect during and after treatment, which can be very important.
Your child's cancer care team will be your first source of information and support, but there are other resources for help when you need it. Hospital- or clinic-based support services can also be an important part of cancer care. These might include nursing or social work services, financial aid, nutritional advice, rehab, or spiritual help. For children and teens with cancer and their families, other specialists can be an important part of care as well.
The American Cancer Society also has programs and services—including rides to treatment, lodging, and more—to help you get through treatment. Call our National Cancer Information Center at 1-800-227-2345 and speak with one of our trained specialists.
The treatment information given here is not official policy of the American Cancer Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor. Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask your cancer care team any questions you may have about your treatment options.
Developed by the American Cancer Society medical and editorial content team with medical review and contribution by the American Society of Clinical Oncology (ASCO).
Aplenc R, Elgarten CW, Choi JK, Meshinchi S. Chapter 17A: Acute Myeloid Leukemia and Myelodysplastic Syndromes. In: Blaney SM, Adamson PC, Helman LJ, eds. Pizzo and Poplack’s Pediatric Oncology. 8th ed. Philadelphia, Pa: Lippincott Williams & Wilkins; 2021.
Gramatges MM, O’Brien MM, Rabin KR. Chapter 16: Acute Lymphoblastic Leukemia. In: Blaney SM, Adamson PC, Helman LJ, eds. Pizzo and Poplack’s Pediatric Oncology. 8th ed. Philadelphia, Pa: Lippincott Williams & Wilkins; 2021.
National Cancer Institute. Childhood Acute Lymphoblastic Leukemia Treatment (PDQ). 2025. Accessed at https://www.cancer.gov/types/leukemia/hp/child-all-treatment-pdq on May 7, 2025.
National Cancer Institute. Childhood Acute Myeloid Leukemia Treatment (PDQ). 2025. Accessed at https://www.cancer.gov/types/leukemia/hp/child-aml-treatment-pdq on May 7, 2025.
National Cancer Institute. Childhood Chronic Myeloid Leukemia Treatment (PDQ). 2024. Accessed at https://www.cancer.gov/types/leukemia/hp/child-aml-treatment-pdq/childhood-cml-treatment-pdq on May 7, 2025.
National Cancer Institute. Juvenile Myelomonocytic Leukemia Treatment (PDQ). 2024. Accessed at https://www.cancer.gov/types/leukemia/hp/child-aml-treatment-pdq/childhood-jmml-treatment-pdq on May 12, 2025.
National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Pediatric Acute Lymphoblastic Leukemia. v.3.2025 - March 17, 2025. Accessed at https://www.nccn.org/professionals/physician_gls/pdf/ped_all.pdf on May 7, 2025.
Rau RE, Loh ML. Chapter 17B: Myeloproliferative Neoplasms of Childhood. In: Blaney SM, Adamson PC, Helman LJ, eds. Pizzo and Poplack’s Pediatric Oncology. 8th ed. Philadelphia, Pa: Lippincott Williams & Wilkins; 2021.
Last Revised: July 22, 2025
American Cancer Society medical information is copyrighted material. For reprint requests, please see our Content Usage Policy.
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