Diagnosis guide · Leukemias
Acute lymphoblastic leukemia (ALL)
If you or someone you love has just heard this diagnosis, start here. It covers several subtypes, and this guide shows how they differ, so you can find the one on your report.
Acute lymphoblastic leukemia is a cancer of immature lymphoid cells. Tests distinguish B-cell ALL from T-cell ALL and identify genetic changes that help guide treatment. Philadelphia-positive ALL is usually a subtype of B-cell ALL, not a third parallel cell type; its BCR::ABL1 change makes targeted medicines relevant. Treatment also depends on age, response to therapy and other risk factors. A donor transplant is considered for selected patients, rather than everyone with ALL.
In short
- Acute lymphoblastic leukemia (ALL) is a cancer of immature lymphoid cells. These are young white blood cells that have not finished developing.
- Tests sort ALL into B-cell or T-cell types and look for gene changes. In Philadelphia-positive ALL, usually a B-cell type, one change makes targeted medicines an option.
- A donor transplant is considered for selected patients, not for everyone with ALL. The cells can come from a relative, an unrelated registry volunteer or cord blood.
3 subtypes
Find the subtype on your report
The exact diagnosis shapes the treatment options. Your care team can explain the name on your report.
B-cell acute lymphoblastic leukemia (B-ALL)
B-cell acute lymphoblastic leukemia (B-ALL) is a fast-growing cancer of immature B lymphocytes. Treatment often controls it without transplant, while donor transplantation and selected immunotherapies are important for some higher-risk or relapsed cases.
Donor transplant optionT-cell acute lymphoblastic leukemia (T-ALL)
T-cell acute lymphoblastic leukemia (T-ALL) is a fast-growing cancer of immature T cells. Treatment uses an ALL regimen; donor transplantation is considered when the response or disease features indicate a substantial risk of relapse.
Donor transplant optionPhiladelphia-positive acute lymphoblastic leukemia (Ph+ ALL)
Philadelphia chromosome-positive ALL is usually a B-lineage acute leukemia containing the BCR::ABL1 fusion. The fusion makes an overactive growth-signaling enzyme, so treatment includes medicines directed at that target.
Donor transplant option
For some of these subtypes, a patient needs a donor who is not a relative. The registry that serves your country explains who can join.
See if you can joinNearby
Related diagnosis guides
What to know
Key facts
- New U.S. cases
- About 6,250 expected in 2026All ages, United States, 2026 projection by the American Cancer Society, as reported by SEER. Source: New U.S. cases
- Philadelphia chromosome
- About 20% of adults with ALL, and a small share of childrenAdults with ALL, as summarized by NCI (Adult ALL PDQ, updated 2025-03-17). Source: Philadelphia chromosome
How ALL is diagnosed
ALL is often first suspected from a complete blood count (CBC), a routine blood test that counts red cells, white cells and platelets. A blood smear looks at the cells under a microscope for immature leukemia cells (blasts). A bone marrow sample, taken with a hollow needle, is then checked for leukemia cells.
Lab tests on the leukemia cells show exactly what kind of ALL it is. Immunophenotyping (often by flow cytometry) reads markers on the cells. It shows whether the leukemia started in B cells, as in about 8 in 10 adults, or in T cells. Chromosome and gene tests (cytogenetics and molecular tests) look for changes that shape treatment. One is the Philadelphia chromosome (BCR::ABL1). It is found in about 20% of adults with ALL and a small share of children.
A spinal tap (lumbar puncture) checks for leukemia cells in the fluid around the brain and spinal cord. Children also have a chest x-ray, to look for a mass of leukemia cells in the middle of the chest. The picture is not complete at diagnosis. How quickly and how far the leukemia falls in the first month of treatment also matters. Tests for measurable residual disease (MRD) track this. They help decide how intense treatment should be and whether a transplant should be considered.
NMDP guidance recommends tissue typing (high-resolution HLA typing) at diagnosis for everyone 40 and older with ALL, so a donor search can start quickly if it is ever needed. It does not mean a transplant is planned.
When transplant specialists are usually consulted
NMDP has two sets of guidance for ALL. For people 40 and older, it recommends high-resolution HLA typing at diagnosis for everyone, and a transplant consultation early after diagnosis. For children and people younger than 40, it lists specific situations. These include some high-risk infants, leukemia that does not go into remission, MRD still found after early treatment, certain high-risk gene changes and a first relapse.
Read the guidanceLooking ahead
Outlook for ALL
Outlook for ALL depends on age, the gene changes in the leukemia cells and how well the leukemia responds to the first treatment. Children do best. For U.S. children younger than 15, five-year survival has risen to about 90%. For teens aged 15 to 19, it is more than 75%. Infants, especially those diagnosed in the first few months of life, face a harder course.
Adults face a harder course too, and younger adults tend to do better than older adults. Still, most adults reach remission: NCI reports that 60% to 80% of adults do after the first phase of treatment (induction). For Philadelphia-positive ALL, treatment that includes targeted pills called tyrosine kinase inhibitors brings remission rates generally above 90%.
A donor stem cell transplant is used for selected people, not everyone. For children and teens, it is rarely part of first treatment and is used more often when ALL comes back. For adults, it is more often considered during the first remission. These are group results. They cannot predict how any one person will do.
About these numbers. Each one says which group of people it comes from, and the place and years where the source gives them. It describes what happened across that group, not what will happen to any one person. And a figure measured among people who had a transplant is not the same as the number of people who need one.
- 73.2%5-year relative survival, ALL, all ages
People of all ages diagnosed with ALL of any type, 2016–2022, U.S. SEER 21 areas (excluding Illinois)
Read the source: 5-year relative survival, ALL, all ages - About 90%5-year survival, children younger than 15
U.S. children younger than 15 with ALL, around 2020 (up from 60% in 1975); NCI PDQ
Read the source: 5-year survival, children younger than 15 - More than 75%5-year survival, teens aged 15 to 19
U.S. adolescents aged 15 to 19 with ALL, around 2020 (up from 28% in 1975); NCI PDQ
Read the source: 5-year survival, teens aged 15 to 19
The all-ages SEER figure mixes children, who do very well, with adults, whose outlook is harder.
Common questions
What is the survival rate for acute lymphoblastic leukemia?
Results differ a lot by age. Children do best, and NCI reports that survival for U.S. children with ALL has risen greatly since the 1970s. Teens do well too, and adults face a harder course. The outlook section on this page gives the figures, with the groups they describe. Group numbers cannot predict one person's outcome.
Is ALL only a childhood cancer?
No. ALL is the most common cancer in children. NCI says it makes up about 25% of childhood cancers in the United States and occurs most often between ages 1 and 4. But it also affects teens and adults. In US SEER data for 2019 to 2023, the median age at diagnosis was 18, which means about half of the people diagnosed were 18 or older.
What is the difference between B-cell and T-cell ALL?
Both are fast-growing cancers of immature lymphoid cells. Tests on the leukemia cells show whether it began in B cells or T cells, and look for genetic changes that help guide treatment. Philadelphia chromosome-positive ALL is usually a type of B-cell ALL, not a third separate kind; its BCR::ABL1 change means targeted medicines can be used. Age, response to treatment and other risk factors also shape the plan.
Does everyone with ALL need a bone marrow transplant?
No. A donor transplant is considered for selected patients rather than everyone with ALL. Many people complete drug treatment without one. NCI notes that for children and teens, a stem cell transplant is rarely the first treatment and is used more often when ALL comes back. Transplant is also considered when the leukemia responds poorly to treatment or has high-risk features.
What are the first symptoms of ALL?
Common early signs include tiredness, fever, pale skin, and easy bruising or bleeding, including tiny red spots under the skin. Some people have bone or joint pain, swollen lymph nodes or a full feeling below the ribs. NCI notes early signs can seem like the flu or other common illnesses. These signs can have many causes, so blood and bone marrow tests are needed to diagnose ALL.
Can a brother or sister be the donor for ALL?
Yes, if their tissue type (HLA) is a close enough match. NCI says a brother or sister is most often the best match. NMDP explains that each brother or sister who has the same parents has a 1 in 4 chance of being a full match, so many patients do not have a fully matched sibling. Unrelated registry volunteers and half-matched parents or children can also be options.
Is childhood leukemia curable?
For most children, yes. Acute lymphoblastic leukemia (ALL) is the most common cancer in children, and it is now very treatable. NCI says about 85% of children aged 1 to 18 on current treatment are expected to live long-term with no relapse or other major setback. Some groups, defined by gene changes and a fast, deep response to treatment, do even better. Infants, teens and adults face a harder course. Group numbers cannot predict how one child will do.
How many children get ALL each year?
NCI estimates that about 3,100 children and teens younger than 20 are diagnosed with ALL each year in the United States. ALL makes up about 1 in 4 cancer diagnoses in children younger than 15. It is most common between ages 1 and 4.
For your next appointment
Acute lymphoblastic leukemia (ALL)
From the Jada Bascom Foundation disease library, jadabascomfoundation.org. Printed .
Questions to bring to your care team
- Is it B-cell or T-cell ALL, and which gene changes were found? What do they change about treatment?
- Is the leukemia Philadelphia-positive, and will a targeted pill be part of treatment?
- When will you check MRD, and what results would make you consider a transplant?
- Would it help for brothers and sisters to have HLA typing now, just in case?
- What is the goal of each treatment you are suggesting?
- What happens if a fully matched donor is not found?
- Where can our family find support during treatment?
A one-page list to take to the next appointment, with room for notes.
Supporting someone with a diagnosisSupport for patients and families
These independent organizations offer information and support. JBF is not affiliated with them.
- Acute Leukemia Advocates Network (ALAN) A worldwide network of acute leukemia patient organizations; its member list helps families look for a group in their country.Worldwide
- Leukaemia Care UK charity with a free helpline, support groups and practical help for anyone affected by leukemia, including families and caregivers.United Kingdom
- Leukemia Research Foundation US nonprofit offering peer support, an online community and mentoring for people with ALL and their families, plus patient education.United States
Ways to help
Someone may be waiting for a match.
Some people with acute lymphoblastic leukemia (ALL) are treated with a transplant from a donor. When no relative matches, that donor is often a stranger who joined a registry.
Join the registry
JBF points you to the official registry that serves your country. It explains who can join and what donation involves.
Help someone you love find a donor
If someone you love needs a donor, our family guide explains practical ways to help. A registration drive can add many potential donors at once, for them and for others.
Support this work
Gifts to the Jada Bascom Foundation support donor-awareness education like this page, community outreach, drive planning and referrals to official registries.
Keep learning
Understanding transplant
Short explainers on what a transplant is and what it means for a family.
Sources and further reading
- Acute Lymphoblastic Leukemia Treatment (PDQ)
National Cancer Institute, Accessed September 5, 2026 - Childhood Acute Lymphoblastic Leukemia Treatment (PDQ)
National Cancer Institute, Accessed September 5, 2026 - Acute Lymphocytic Leukemia — Cancer Stat Facts
National Cancer Institute, SEER Program, Accessed 2026-09-24 - Childhood Acute Lymphoblastic Leukemia Treatment (PDQ), Health Professional Version
National Cancer Institute, Accessed 2026-09-24 - What Is Acute Lymphocytic Leukemia (ALL)?
American Cancer Society, Accessed 2026-09-24 - Acute lymphoblastic leukemia (ALL) — HCT consultation timing guidelines
NMDP, Accessed 2026-09-24 - Stem Cell and Bone Marrow Transplants for Cancer
National Cancer Institute, Accessed 2026-09-24 - What is HLA? HLA Basics, Typing & Matching
NMDP, Accessed 2026-09-24 - Adult Acute Lymphoblastic Leukemia Treatment (PDQ), Health Professional Version
National Cancer Institute, 2025-03-17 - Transplant consultation guidelines: Acute lymphoblastic leukemia (ALL) – pediatric (defined as younger than 39)
NMDP, Accessed 2026-09-26

