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Also called: acute lymphocytic leukemia, acute lymphoid leukemia, ALL
Acute lymphoblastic leukemia (ALL) is a cancer of the blood and bone marrow. Bone marrow is a soft, sponge-like tissue in the center of many bones. It makes blood cells.
The bone marrow makes 3 types of blood cells:
In ALL, the bone marrow makes too many white blood cells (lymphocytes) that do not work correctly. There is no room for healthy cells to develop. As a result, children and teens cannot fight infections well. They can get very sick. ALL is the most common form of childhood leukemia and the most common form of childhood cancer overall. About 3 in 4 children and teens with leukemia have ALL. Doctors often do not know why leukemia happens. It is not because of anything the child or family did.
Learn more about acute lymphoblastic leukemia on the Together by St. Jude™ online resource.
Chemotherapy is the main treatment for ALL. It has 3 phases and can take 2–2.5 years to complete.
The treatment plan depends on the chance that the leukemia may not respond to treatment or may come back after treatment has finished. This is called risk-based treatment.
St. Jude groups ALL cases as low risk, standard risk, and high risk. Cases that are most likely to respond to treatment are low risk. Leukemia that is the hardest to treat is high risk.
Children with low-risk ALL get less medicine than children with standard-risk ALL. Children with high-risk ALL get more medicine than children with standard-risk ALL. They may need more treatments such as immunotherapy or stem cell (bone marrow) transplant.
For specific types of ALL, children may get targeted therapy or immunotherapy. These therapies help the body identify and kill certain types of cancer cells.
Your child’s oncologist will discuss treatment options with you.
St. Jude offers clinical trials and cancer research studies for children, teens, and young adults for ALL. Learn more about clinical research at St. Jude.
Study goal:
The main purpose of this study is to find the highest dose of CD123-CAR T cells that is safe to give patients with AML. We also want to study the side effects of the treatment and learn how effective it is in fighting this type of cancer.
Age:
21 years old or younger
Study goal:
The main goal of this study is to learn about the good and bad side effects of inotuzumab ozogamicin in children with this type of leukemia and to find out how well the drug works to get rid of the disease.
Age:
Younger than 22 years old
Study goal:
The main goal of this research study is to help us learn how to better treat pain and symptoms in children going through chemotherapy cancer treatment.
Age:
8 to 18 years old
Study goal:
The main goal of this study is to learn the largest dose of memory CAR T cells that can be safely given. Researchers also want to learn about the way memory CAR T cells act in the body and how effectively they treat this type of cancer.
Age:
Donor: At least 19 years old; Recipient: 21 years or younger
Study goal:
The purpose of this study is to find the highest dose of CD70+ CAR cells that is safe to give to patients with CD70+ blood cancers.
Age:
Up to 21 years old
Study goal:
1) To find out how many long-term survivors of leukemia have iron overload by using MRI testing. 2) To study how the number of red blood cell transfusions you received determines whether you have iron overload. 3) To explore how your age at the time of cancer therapy, the length of time from therapy, and gender affects whether you develop iron overload. 4) To find out if iron overload is causing problems with your organs.
Study goal:
To find the best dose of SNDX-5613 to use along with chemotherapy for young patients with KMT2A-R leukemia
Age:
1 month to 5 years old
Study goal:
To study if using OXPHOS MRI, muscle function testing, and analysis of blood and muscle biopsies can help us understand the link between cancer, cancer treatment, and muscle weakness in acute lymphoblastic leukemia survivors. Learn more.
Age:
18 years and up
Patients accepted to St. Jude must have a disease we treat and must be referred by a physician or other qualified medical professional. We accept most patients based on their ability to enroll in an open clinical trial.
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