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Acute lymphoblastic leukemia (ALL) treatment

It's important that your doctor is experienced in treating patients with acute lymphoblastic leukemia (ALL) or has access to an ALL blood cancer specialist when treating ALL.

The information on this page covers treatment for adults with ALL. Visit childhood ALL to learn about signs and symptoms, diagnosis, and treatment information for children with ALL. 

Pre-treatment considerations 

Adults of childbearing age should ask the doctor for information about addressing the risk of infertility. Read our free publication, Fertility and Cancer, for more details.

Prognostic factors and pre-treatment testing 

Before you start treatment, your doctor will perform tests to learn more about your overall health and your leukemia, including determining whether the leukemia has spread to other parts of your body. Doctors use this information for treatment planning.  

Certain factors can affect a patient’s “prognosis,” which is the likely outcome of their disease. Doctors use “prognostic factors” to help predict how a patient’s disease is likely to respond to treatment.  

Prognosis and treatment options may depend on the following factors: 

  • Patient age
  • Number of white blood cells in the blood at the time of diagnosis
  • ALL subtype
  • Changes in the chromosomes and/or genes in the leukemia cells
  • Response to initial treatment (induction)
  • Whether leukemia cells are found in the central nervous system (brain and spinal cord) 

Tests used for pre-treatment planning include: 

  • Blood tests
  • Lumbar puncture to examine fluid in the spinal column for ALL cells
  • Imaging tests, such as computed tomography (CT) scans, positron emission tomography (PET) scans, and magnetic resonance imaging (MRI), to check for leukemia cells in lymph nodes or organs
  • Echocardiogram to check heart function 

Learn more about lab and imaging tests. 

Types of treatment for ALL 

Doctors use several types of approaches and treatment combinations for ALL. Open each section below to learn more.

Because of ALL's rapid growth, most patients need to start chemotherapy soon after diagnosis. 

Chemotherapy drugs kill fast-growing cells throughout the body, including cancer cells and normal, healthy cells. The damage to normal, healthy cells can cause side effects. Not everyone experiences side effects the same way.  

ALL chemotherapy treatment consists of multiple phases. Open each section below to learn more.

 

The first phase of treatment is induction therapy. The goal of induction therapy is to destroy as many cancer cells as possible in order to achieve (induce) a remission. Typically, initial therapy requires a hospital stay of four to six weeks. 

Induction regimens for ALL generally use a combination of drugs that include: 

  • Vincristine (Oncovin®)
  • Anthracyclines (daunorubicin (Cerubidine®), doxorubicin (Adriamycin®))
  • Corticosteroids (prednisone, dexamethasone) 

The doctor may add additional drugs to induction based on the patient’s prognostic factors. 

During induction, patients also receive treatment to prevent ALL from spreading to the central nervous system. This is called CNS-directed treatment. 

At the end of induction therapy, doctors will check to see whether the patient has achieved a complete remission. A complete remission is achieved when you no longer have signs and symptoms of leukemia.  

If you are in remission, you will continue on to the next phase of treatment called “consolidation.” If you are not in remission, another course of chemotherapy is usually given.  

To see a list of standard drugs and drugs under clinical study to treat ALL, order or download our free booklet, Acute Lymphoblastic Leukemia (ALL) in Adults.

Minimal residual disease (MRD): Even when a complete remission is achieved, some leukemia cells that cannot be seen with a microscope may remain in the body. The presence of these cells is referred to as “minimal residual disease (MRD).”  

Patients who have achieved remission after initial treatment for this type of ALL but have MRD are at increased risk of disease relapse. 

It is important to get tested for MRD after achieving remission. The tests used most often to detect MRD are flow cytometry, polymerase chain reaction (PCR), and next-generation sequencing. These three tests typically use samples of bone marrow cells, but in some cases, blood samples can be used.  

These tests are much more sensitive than standard tests that examine cell samples with a microscope. It is often recommended that MRD testing be done after the completion of induction therapy. Recommendations for additional MRD testing depend on the treatment regimen used. 

Learn more about blood cancer tests that help doctors identify MRD: 

 

For patients in remission but who test positive for MRD, blinatumomab (Blincyto®) may be prescribed. For information about the drugs listed on this page, visit our cancer drug listings. 

The second phase of chemotherapy is called “consolidation” therapy or "intensification" therapy. The goal of consolidation is to kill any remaining leukemia cells. Consolidation treatment is often based on whether the patient is MRD positive after induction. For patients with B-cell ALL who are MRD positive, blinatumomab (Blincyto®) is often the recommended treatment. 

For patients who are MRD negative after induction, consolidation is typically combination chemotherapy. Depending on the treatment regimen used, consolidation chemotherapy may use different drugs than those given during induction or some of the same drugs.  

As part of consolidation therapy, some patients in remission may receive a stem cell transplantation. 

The third phase of ALL chemotherapy treatment is called “maintenance.” The goal of maintenance therapy is to prevent disease relapse after induction and consolidation therapy. It usually lasts for about two years. Patients receive lower doses of chemotherapy drugs and, as a result, tend to have less severe side effects. Most maintenance therapy regimens include 6-mercaptopurine, methotrexate, vincristine, and corticosteroids.

ALL can spread to the central nervous system (the brain and spinal cord). A lumbar puncture (also called a spinal tap) is used to check the spinal fluid for ALL cells. At the time of diagnosis, it is uncommon for leukemia cells to be found in the central nervous system, occurring in only 3 percent to 7 percent of cases. 

Even if ALL cells are not found in the spinal fluid, patients are still treated to prevent the spread of leukemia cells to the central nervous system. CNS-directed therapy is typically given to all patients throughout the entire course of ALL therapy, from induction to consolidation and throughout maintenance.  

CNS-directed therapy may include: 

  • Intrathecal chemotherapy: In this treatment, chemotherapy is injected directly into the spinal canal
  • Systemic chemotherapy: In this treatment, drugs are given through a vein
  • Cranial irradiation: In this treatment, patients receive radiation therapy to the brain. In most practices, doctors do not routinely use cranial radiation except in patients who already have leukemia cells in their central nervous system. Some regimens for T-cell ALL still use cranial radiation, although this is becoming less common. When radiation therapy is used, the chance of long-term side effects is higher.  

For information about the drugs listed on this page, visit our cancer drug listing. 

The goal of stem cell transplantation is to cure the patient’s cancer by destroying the cancer cells in the bone marrow with high doses of chemotherapy and then replacing them with new, healthy blood-forming stem cells. The healthy blood stem cells will grow and multiply, forming new bone marrow and blood cells. 

Stem cell transplantation is not used as the first or primary treatment for ALL. It may be used as a treatment for high-risk ALL patients or for patients who do not respond to treatment. Stem cell transplantation is a complex treatment. It can cause serious side effects that can be life threatening, so it may not be a treatment option for every ALL patient. Talk to your doctor about whether stem cell transplantation is a treatment option for you. 

There are two main types of stem cell transplantation:  

  • Allogeneic: patients receive stem cells from a matched or a partially mismatched related donor or an unrelated donor
  • Autologous: patients receive their own stem cells  

Open each section to learn more.

Allogeneic stem cell transplantation involves transferring stem cells from a healthy person (the donor) to the patient. 

The goals of an allogeneic transplant are to: 

  • Restore the body’s ability to make normal blood cells after high-dose chemotherapy
  • Cure the patient of ALL by killing any remaining ALL cells 

To prepare for the transplant, the patient receives high-intensity chemotherapy, either with or without radiation, to kill the remaining leukemic cells in the body. Unfortunately, this also destroys normal stem cells in the bone marrow. Then, the patient receives infusions of the donor stem cells. The donated stem cells restore the bone marrow's ability to form new blood cells. 

Donor stem cells come from a human leukocyte antigen (HLA)-matched or partially mismatched: 

  • Family member
  • Unrelated donor
  • Umbilical cord blood unit 

An allogeneic transplant is a high-risk procedure. Doctors are working to make allogeneic transplants safer. An allogeneic transplant may be a choice for an adult ALL patient if: 

  • They are not responding well to other treatments
  • The expected benefits of an allogeneic transplant exceed the risks
  • There is a stem cell donor 

The upper age limit for an allogeneic transplant depends on the treatment center. 

Learn more about allogeneic stem cell transplantation.

Reduced-intensity allogeneic stem cell transplantation 

A reduced-intensity allogeneic transplant uses lower doses of chemotherapy than a standard allogeneic transplant; it does not completely inactivate the patient’s immune system or treat the ALL as aggressively. Some older and sicker patients may be helped by this treatment.

Graft-versus-host disease 

A serious risk of allogeneic and reduced-intensity allogeneic stem cell transplantation is graft-versus-host disease (GVHD), which develops if the donor's immune cells attack  normal tissue. GVHD's effects can range from minor to life threatening. 

An autologous transplant uses the patient’s own stem cells. Your doctor will talk with you about whether an autologous transplant is a treatment option for you. It is not commonly used to treat ALL. This is because of the high relapse rate following this type of transplant. 

Learn more about stem cell transplantation. 

About 25 percent of adults with ALL have a subtype called “Ph-positive ALL” (also known as “Ph+ ALL” or “Philadelphia chromosome-positive ALL”). These people’s leukemia cells have the Philadelphia chromosome, formed by a “translocation” between parts of chromosomes 9 and 22; that means that a piece of chromosome 9 broke off and attached itself to chromosome 22; and a piece of chromosome 22 similarly breaks off and attaches to chromosome 9. The abnormal chromosome 22 is known as the Philadelphia chromosome.  

This chromosomal alteration creates a fusion gene called BCR-ABL1. This gene produces a protein called a tyrosine kinase that causes the leukemia cells to grow and divide out of control. 

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Tyrosine kinase inhibitors (TKIs)  

Tyrosine kinases are enzymes that are a part of many cell functions including cell signaling, growth, and division. These enzymes may become too active in patients with Philadelphia chromosome-positive ALL (Ph+ ALL). 

TKIs work to block these overactive enzymes and may stop cancer cells from growing. TKIs are pills taken by mouth. They are generally not used alone to treat ALL. Instead, they are added to other medications, such as a combination chemotherapy regimen. TKIs used in the treatment of Ph+ ALL include: 

  • Imatinib (Gleevec®)
  • Dasatinib (Sprycel®)
  • Ponatinib (Iclusig®)
  • Bosutinib (Bosulif®)
  • Nilotinib (Tasigna®) 

Common side effects of TKIs include low blood counts, abnormal bleeding, pain, nausea and vomiting, diarrhea, fatigue, rashes, headaches, and pain in muscles, bones, and joints. TKIs may also cause fluid to collect under the eyes and in the hands, feet, or lungs. Uncommon but serious side effects include a change in the rhythm of the heart, inflammation of the pancreas, blood vessel narrowing, or blood clot formation. 

Another 10 percent to 30 percent of adults who have ALL have a subtype known as “Philadelphia chromosome-like ALL” (Ph-like ALL). Unlike those with Ph+ ALL, who share a similar genetic mutation, patients with Ph-like ALL have a highly diverse range of genetic mutations that activate tyrosine kinase signaling. Recent studies have analyzed the genetic profile of patients with some subsets of Ph-like ALL and found that using TKIs and other targeted therapies may help treat these types of leukemia. These patients require special attention as Ph-like ALL is more resistant to standard chemotherapy and may require allogeneic transplant in first remission. 

Taking part in a clinical trial may be the best treatment choice for some ALL patients. Clinical trials are under way for patients at every treatment stage and for patients in remission. Today's standard treatments for cancer are based on earlier clinical trials. LLS continues to invest in ALL research. 

Learn more about clinical trials


Get free clinical trial support! Visit our Clinical Trial Support Center (CTSC).

Connect with registered nurses with expertise in blood cancers who can personally assist you or your caregiver through each step of the clinical trial process. 


Finding the best treatment approach 

If you have ALL, you should begin treatment as soon as possible after diagnosis. If time allows, however, you may want to seek a second opinion. A second opinion may help you to feel more confident about the chosen treatment plan.  

Your doctor will recommend a treatment based on several factors:   

  • Your ALL subtype
  • The stage and category of the disease
  • Disease that has not responded to treatment, called refractory disease
  • Disease that has come back after treatment, called relapsed disease
  • Your age
  • Other medical problems, such as diabetes or heart or kidney disease 

Some things that may affect the outcome of your ALL treatment are: 

  • Your ALL subtype
  • The results of your lab tests
  • Your age and general health
  • Your medical history, including whether you were treated before with chemotherapy
  • Whether you have a serious infection at the time of diagnosis, ALL in your central nervous system, or ALL that has not responded to treatment or has relapsed
  • As you develop a treatment plan with your doctor, be sure to discuss:
  • The results you can expect from treatment
  • The possibility of participating in a clinical trial, where you'll have access to advanced medical treatment that may be more beneficial to you than standard treatment
  • Potential side effects, including long-term and late effects 

Learn more about communicating with your blood cancer specialist or find lists of suggested questions to ask your healthcare providers.

ALL treatment side effects and complications

Therapy for ALL can produce side effects. For most patients, treatment side effects are temporary and go away once therapy ends. For other patients, side effects can be severe, sometimes requiring hospitalization. 

Before you start treatment, talk with your doctor about potential side effects. Drugs and other therapies can prevent or manage many side effects.

You may experience side effects depending on:  

  • The intensity of chemotherapy
  • The drugs used during therapy
  • Overall health and whether you have any chronic health conditions, such as diabetes or kidney disease 

There are common side effects to ALL and its treatment, especially chemotherapy and stem cell transplantation. Open each section below to learn more.

ALL can cause a decrease in normal blood cell production. Chemotherapy is toxic to both normal blood cells and ALL cells, making the number of healthy cells decrease. 

Learn more about infections, iron overload, or low blood counts and how to manage them. 

The infection risk increases during chemotherapy when the body doesn't produce enough white cells to keep the immune system working properly. 

Learn more about infections, iron overload, or low blood counts and how to manage them.

Patients may experience bone pain due to leukemia cells in the bone marrow. Some chemotherapy medications may cause peripheral neuropathy, a nerve problem that can cause pain, numbness, and tingling in the hands and feet.

Learn more about disease- and treatment-related pain and how to manage it.

Patients who undergo an allogeneic stem cell transplantation are at risk of developing graft-versus-host disease (GVHD). GVHD develops when the donor's immune cells mistakenly attack the patient's normal cells. GVHD can be mild, moderate, or severe—even life threatening. 

Learn more about graft-versus-host disease (GVHD).  

TLS is characterized by metabolic abnormalities caused by the sudden release of the cellular contents of dying cells into the bloodstream, which is induced by chemotherapy. If untreated, TLS can lead to heart arrhythmias, seizures, loss of muscle control, acute kidney failure, and even death. Patients with leukemia are constantly monitored for the development of TLS and are given drugs, such as allopurinol (Zyloprim®) or rasburicase (Elitek®), to prevent or lessen the effects of this condition.  

Learn more about TLS. 

The following side effects are also common: 

  • Mouth sores
  • Diarrhea
  • Hair loss
  • Rashes
  • Nausea and vomiting
  • Headaches
  • Loss of appetite
  • Fatigue
  • Neuropathy—numbness, tingling, or muscle weakness (usually in the hands or feet)   

Learn more about blood cancer treatment side effects and how to manage them 

Treatment results 

Treatment results and outcomes vary among patients. Newer treatment therapies, progress in stem cell transplantation, better supportive care, and studies of new drugs in clinical trials are all contributing to improved outcomes and quality of life for people diagnosed with blood cancers. 

Relapsed and refractory ALL 

Some patients have residual leukemia cells in their bone marrow even after they receive intensive treatment. In these cases, the disease is referred to as being “refractory” (or “refractory ALL”). 

Other patients achieve remission but later have decreased numbers of normal blood cells and a return of leukemia cells in their bone marrow. This is referred to as a “relapse” of the disease (or “relapsed ALL”).  

Relapsed/refractory disease is generally more difficult to treat, but there are treatment options available. Treatment for relapsed/refractory ALL is usually more intensive or complex than the treatment used following initial diagnosis. For these reasons, it is particularly important to consider getting opinions on treatment options from someone with expertise in managing relapsed/refractory ALL. 

At the time of relapse, genetic testing of the leukemia cells may be performed. The mutational pattern at the time of relapse may be different from when the disease was first diagnosed, and this can affect treatment decisions. 

Treatments for relapsed/refractory ALL

Treatments for relapsed/refractory ALL may include: 

  • A clinical trial
  • Chemotherapy
  • For patients with Ph+ALL, a TKI given alone or as part of a chemotherapy regimen. In some cases, the TKI may be combined with a corticosteroid. If the TKI is part of a chemotherapy regimen, this regimen will usually be different from the one used during initial therapy. For some older patients who cannot tolerate chemotherapy, using a TKI along with a corticosteroid may be an option.
  • Nelarabine for patients with T-cell ALL
  • Blinatumomab (Blincyto®)
  • Inotuzumab ozogamicin (Besponsa®)
  • Revumenib (Revuforj®)
  • Allogeneic stem cell transplantation for physically fit patients with an available donor. Some older patients, as well as patients in poor health, may not be able to tolerate such an intense treatment.
  • CAR T-cell therapy, including:
  • Tisagenlecleucel (Kymriah®)
  • Brexucabtagene autoleucel (Tecartus®)
  • Obecabtagene autoleucel (Aucatzyl®) 

For information about the drugs listed on this page, visit our cancer drug listing.

Long-term and late effects of treatment 

For some people, side effects may last or appear well after treatment is finished.

Learn more about the long-term and late effects of treatment.

Follow-up care  

Find more information about follow-up care, including what to expect, long-term, and late effects of treatment, survivorship clinics, and other resources, such as The National Comprehensive Cancer Network (NCCN) treatment guidelines. 

Use the Survivorship Workbook to collect all the important information you need throughout diagnosis, treatment, follow-up care, and long-term management of a blood cancer.

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T-cell acute lymphoblastic leukemia (T-ALL)

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acute lymphoblastic leukemia (ALL)

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acute lymphoblastic leukemia (ALL)

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acute lymphoblastic leukemia (ALL)

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acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML)

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pre-B-cell acute lymphoblastic leukemia (pre-B-ALL)

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acute lymphoblastic leukemia (ALL)

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Maverick

B-cell acute lymphoblastic leukemia (B-ALL)

Rex

Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL)

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acute myeloid leukemia (AML+MLLr)

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