The usual doses of chemotherapy drugs can cause serious side effects to quickly dividing tissues such as the bone marrow. Unfortunately, in many cases standard doses of chemotherapy aren't able to cure ALL. Even though higher doses of these drugs might be more effective, they are not given because they could severely damage the bone marrow, which is where new blood cells are formed. This could lead to life-threatening infections, bleeding, and other problems due to low blood cell counts.
A stem cell transplant (SCT) allows doctors to use higher doses of chemotherapy and, sometimes, radiation therapy. After treatment is finished, the patient receives a transplant of blood-forming stem cells to restore the bone marrow.
Blood-forming stem cells used for a transplant are obtained either from the blood (for a peripheral blood stem cell transplant, or PBSCT) or from the bone marrow (for a bone marrow transplant, or BMT). Bone marrow transplants were more common in the past, but they have largely been replaced by PBSCT.
Types of transplants
There are 2 main types of stem cell transplants: allogeneic and autologous. They differ in the source of the blood-forming stem cells.
Allogeneic stem cell transplant: In an allogeneic transplant, the stem cells come from someone else -- usually a donor whose tissue type is almost identical to the patient's. Tissue type is based on certain substances on the surface of cells in the body. These substances can cause the immune system to react against the cells. Therefore, the closer a tissue "match" is between the donor and the recipient, the better the chance the transplanted cells will "take" and begin making new blood cells.
The donor may be a brother or sister if they are a good match. Less often, a matched unrelated donor (MUD) may be found. The stem cells from an unrelated donor come from volunteers whose tissue type has been stored in a central registry and matched with the patient’s tissue type. Sometimes umbilical cord stem cells are used. These stem cells come from blood drained from the umbilical cord and placenta after a baby is born and the umbilical cord is cut.
An allogeneic stem cell transplant may be more effective than an autologous transplant because of the "graft versus leukemia" effect. When the donor immune cells are infused into the body, they may recognize any remaining leukemia cells as being foreign to them and will attack them. This effect doesn't happen with autologous stem cell transplants.
An allogeneic transplant is the preferred type of transplant for ALL when it is available, but its use is limited because of the need for a matched donor. Its use is also limited by its side effects, which are too severe for most people over 55 to 60 years old.
Autologous stem cell transplant: In an autologous transplant, a patient's own stem cells are removed from his or her bone marrow or peripheral blood. They are frozen and stored while the person gets treatment (high-dose chemotherapy and/or radiation). A process called purging may be used to try to remove any leukemia cells in the samples. The stem cells are then reinfused into the patient's blood after treatment.
Autologous transplants are sometimes used for people with ALL who are in remission after initial treatment. Some doctors feel that it is better than standard consolidation chemotherapy (see "Typical treatment of acute lymphocytic leukemia"), but not all doctors agree with this.
One problem with autologous transplants is that it is hard to separate normal stem cells from leukemia cells in the bone marrow or blood samples. Even after purging (treating the stem cells in the lab to try to kill or remove any remaining leukemia cells), there is the risk of returning some leukemia cells with the stem cell transplant.
The transplant procedure
Blood-forming stem cells from the bone marrow or peripheral blood are collected, frozen, and stored. The patient receives high-dose chemotherapy and sometimes also radiation treatment to the entire body. (Radiation shields are used to protect the lungs, heart, and kidneys from damage during radiation therapy.)
The treatments are meant to destroy any cancer cells in the body. They also kill the normal cells of the bone marrow and the immune system. After these treatments, the frozen stem cells are thawed and given as a blood transfusion. The stem cells settle into the patient's bone marrow over the next several days and start to grow and make new blood cells.
In an allogeneic SCT, the person getting the transplant may be given drugs to keep the new immune system in check. For the next few weeks the patient gets regular blood tests and supportive therapies as needed, which might include antibiotics, red blood cell or platelet transfusions, other medicines, and help with nutrition.
Usually within a couple of weeks after the stem cells have been infused, they begin making new white blood cells. This is followed by new platelet production and, several weeks later, new red blood cell production.
Patients usually stay in the hospital in protective isolation (guarding against exposure to germs) until their white blood cell count rises above 500. They may be able to leave the hospital when their white blood cell count is near 1,000. The patient is then seen in an outpatient clinic almost every day for several weeks. Because platelet counts take longer to return to a safe level, patients may get platelet transfusions as an outpatient.
Practical points
Bone marrow or peripheral blood SCT is a complex treatment. If the doctors think a patient may benefit from a transplant, it should be done at a hospital where the staff has experience with the procedure and with managing the recovery phase. Some bone marrow transplant programs may not have experience in certain types of transplants, especially transplants from unrelated donors.
SCT is very expensive (more than $100,000) and often requires a lengthy hospital stay. Because some insurance companies may view it as an experimental treatment, they may not pay for the procedure. It is important to find out what your insurer will cover before deciding on a transplant to get an idea of what you might have to pay.
Possible side effects
Side effects from SCT are generally divided into early and long-term effects.
The early complications and side effects are basically the same as those caused by any other type of high-dose chemotherapy (see the "Chemotherapy" section of this document), and are due to damage to the bone marrow and other quickly dividing tissues of the body. They can include low blood cell counts (with fatigue and an increased risk of infection and bleeding), nausea, vomiting, loss of appetite, mouth sores, and hair loss.
One of the most common and serious short-term effects is the increased risk for infection from bacteria, viruses, or fungi. Antibiotics are often given to try to prevent infections. Other side effects, like low red blood cell and platelet counts, may require blood product transfusions or other treatments.
Some complications and side effects can persist for a long time or may not occur until months or years after the transplant. These include:
- Graft-versus-host disease (GVHD), which can occur in allogeneic (donor) transplants. This happens when the donor immune system cells attack tissues of the patient's skin, liver, and digestive tract. Symptoms can include weakness, fatigue, dry mouth, rashes, nausea, diarrhea, yellowing of the skin and eyes (jaundice), and muscle aches. In severe cases, GVHD can be life-threatening. GVHD is often described as either acute or chronic, based on how soon after the transplant it begins. Drugs that weaken the immune system are often given to try to keep GVHD under control.
- damage to the lungs, causing shortness of breath
- damage to the ovaries in women, causing infertility and loss of menstrual periods
- damage to the thyroid gland that causes problems with metabolism
- cataracts (damage to the lens of the eye that can affect vision)
- bone damage called aseptic necrosis (where the bone dies because of poor blood supply). If damage is severe, the patient will need to have part of the bone and the joint replaced.
Graft-versus-host disease is the most serious complication of allogeneic (donor) stem cell transplants. It occurs because the immune system of the patient is taken over by that of the donor. The donor immune system then begins reacting against the patient's other tissues and organs.
The most common symptoms are severe skin rashes and severe diarrhea. The liver and lungs may also be damaged. The patient may also become tired easily and have muscle aches. Sometimes GVHD becomes chronic and disabling and, if it is severe enough, can be life-threatening. Drugs that affect the immune system may be given to try to control it.
On the positive side, graft-versus-host disease also leads to "graft-versus-leukemia" activity. Any leukemia cells remaining after the chemotherapy and radiation therapy may be killed by the immune reaction of the donor cells.
Non-myeloablative transplant (mini-transplant)
Many people over the age of 55 will not be able to tolerate a standard allogeneic transplant that uses high doses of chemotherapy. Some, however, may be able to have a non-myeloablative transplant (also known as a mini-transplant or reduced-intensity transplant), where they receive lower doses of chemotherapy and radiation that do not completely destroy the cells in their bone marrow. Then they receive the allogeneic (donor) stem cells. These cells enter the body and establish a new immune system, which sees the leukemia cells as foreign and attacks them (a "graft-versus-leukemia" effect).
Doctors have learned that if they use smaller doses of certain chemotherapy drugs and lower doses of total body radiation, an allogeneic transplant can still sometimes work with much less toxicity. In fact, a patient can receive a non-myeloablative transplant as an outpatient. The major complication is graft-versus-host disease.
Many doctors still consider this procedure to be experimental, and studies are under way to determine how useful it may be against ALL.
For more information on stem cell transplants, see our document, Bone Marrow & Peripheral Blood Stem Cell Transplants.
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