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Because of acute lymphoblastic leukemia's (ALL's) fast growth, most patients need to start chemotherapy soon after diagnosis. During chemotherapy, you're given potent drugs that must be toxic enough to damage or kill leukemic cells. At the same time, they can take aim at normal cells and cause side effects. Yet, not everyone experiences side effects and people react differently.

ALL treatment is generally done in two parts:

  • induction therapy
  • postremission (consolidation and maintenance) therapy

Induction Therapy

The first phase of treatment is induction therapy. Its goal is to "induce" (encourage) remission - when no evidence of the disease is left. Several drugs are combined. Induction therapy attempts to:

  • kill as many ALL cells as possible
  • get blood cell counts back to normal
  • get rid of all signs of the disease for an extended period

Induction therapy is usually done over four to six weeks. You'll likely spend most of that time in the hospital. You may have to go through several rounds of induction therapy before all your ALL cells are destroyed and you go into remission.

Chemotherapy Drugs Used for ALL

Doctors commonly combine two or more chemotherapy drugs to treat ALL. Each drug type works in a different way to kill the cancerous cells. Combining drug types can strengthen their effectiveness.

Some drugs used to treat ALL are:

  • clofarabine (Clolar®)
  • cytarabine (ara-C, Cytosar-U®)
  • daunorubicin (Cerubidine®)
  • methotrexate (Rheumatrex®, Trexall®)
  • mitoxantrone (Novantrone®)
  • cyclophosphamide (Cytoxan®)
  • vincristine (Oncovin®)
  • pegaspargase (Oncaspar®)
  • imatinib mesylate (Gleevec®)
  • prednisone
  • dexamethasone (Decadron®)

The Food and Drug Administration has approved some drugs for special uses, such as:

  • clofarabine (Clolar®), for patients aged 1 to 21 years with relapsed or refractory ALL after they have received at least two prior chemotherapy regimens
  • nelarabine (Arranon®), for patients with relapsed T-cell ALL
  • imatinib mesylate (Gleevec®) and dasatinib (Sprycel®) for patients with PH-positive ALL
  • nilotinib (Tasigna®), being studied in clinical trials for patients with PH-positive ALL
  • vincristine sulfate liposome injection (Marqibo®) to treat adults with PH-negative ALL whose leukemia has relapsed two or more times, or whose leukemia has progressed following two or more regimens of anti-leukemia therapy

If you would like to read about these drugs individually, including information about side effects, click here.

ALL drugs are administered in several ways: You may be given the drugs as pills to swallow, by injection or through a catheter (a thin, flexible tube or intravenous line) surgically placed in a vein, normally in your upper chest.

To see a list of standard drugs and drugs under clinical study to treat ALL, order or download The Leukemia & Lymphoma Society's free booklet Acute Lymphoblastic Leukemia.

Minimal Residual Disease

Some people with ALL have a very low level of remaining ALL cells after treatment. This is called minimal residual disease (MRD). Sensitive molecular techniques permit the identification of small amounts of residual leukemia cells at times when blood and marrow appear normal. Your doctor may consider giving you additional treatment if MRD is detected at the end of your induction therapy (day 29). In some pediatric institutions, doctors are checking for MRD on day eight as an indicator of slow early-responders. The molecular test can also be used for patients in remission to help determine whether more treatment is needed.

Postremission Therapy

After you finish induction therapy and are in remission, you'll begin the second phase of treatment called postremission therapy (consolidation and maintenance therapy). Without this second step, your cancer will likely return.

Consolidation therapy is usually given in cycles for four to six months. You'll continue to receive therapy for two to three years. Maintenance therapy is usually given for about two years. Its purpose is to destroy stray ALL cells that blood or marrow tests can't detect. For most people, postremission therapy includes different drugs than those used during induction therapy.

Some factors your doctor considers when deciding the type of postremission therapy you'll need include:

  • whether induction therapy killed your ALL cells
  • your ability to tolerate intensive treatment
  • cytogenetic findings and whether they reveal certain changes to your chromosomes
  • the availability of a stem cell donor

Some types of ALL, such as T-cell ALL, infant ALL and adult ALL, are usually treated with higher doses of drugs during induction and consolidation and maintenance therapy.

Central Nervous System Prophylaxis

Cancer cells often collect in the lining of the spinal canal or brain (the meninges) in patients with acute lymphocytic leukemia (ALL). This results in central nervous system (CNS) leukemia, which causes headache, nausea, vomiting and blurred vision. Even if cancerous cells aren't detected once you're in remission, you must still undergo central nervous system prophylaxis to ensure that no ALL cells are present.

Intrathecal therapy is used to kill ALL cells in the central nervous system, whether or not their presence is detected. During this procedure, chemotherapy drugs are delivered directly into your spinal canal.

When you undergo intrathecal therapy, your doctor performs a lumbar puncture (spinal tap) by inserting a needle into your spinal canal while you're under heavy sedation or anesthesia. He or she removes spinal fluid, which is examined for leukemic cells, and replaces it by injecting fluid containing chemotherapy drugs such as methotrexate (Rheumatrex®, Trexall®), cytarabine (Cytosar-U®, cytosine arabinoside, ara-C) or hydrocortisone.

Because the drugs go directly into your spinal canal, the therapy more effectively treats hard-to-reach spine and brain cells than injecting chemotherapy into a vein. In some cases, radiation therapy to the spine or brain may be used.

You'll need to undergo a lumbar puncture periodically to ensure that ALL cells are being killed.

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last updated on Wednesday, April 24, 2013
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