- How is Hodgkin disease treated?
- Chemotherapy for Hodgkin disease
- Radiation therapy for Hodgkin disease
- Monoclonal antibodies for Hodgkin disease
- High-dose chemotherapy and stem cell transplant for Hodgkin disease
- Clinical trials for Hodgkin disease
- Complementary and alternative therapies for Hodgkin disease
- Treating classic Hodgkin disease, by stage
- Treating nodular lymphocyte predominant Hodgkin disease (NLPHD)
- Treating Hodgkin disease in children
- Hodgkin disease in pregnancy
- More treatment information
High-dose chemotherapy and stem cell transplant for Hodgkin disease
Stem cell transplants (SCTs) are sometimes used for Hodgkin disease that is hard to treat, such as those that don’t go away completely after chemotherapy and/or radiation, or those that come back after treatment.
The doses of chemotherapy drugs normally are limited by the side effects these drugs cause. Higher doses can’t be used, even if they might kill more cancer cells, because they would severely damage the bone marrow, where new blood cells are made.
A stem cell transplant lets doctors use higher doses of chemotherapy (sometimes along with radiation therapy). After getting high-dose treatment, the patient receives a transplant of blood-forming stem cells to restore the bone marrow.
Blood-forming stem cells used for a transplant come 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). Peripheral blood stem cells are obtained from a procedure similar to a blood donation, while bone marrow donation is usually done in an operating room with the marrow donor under general anesthesia (in a deep sleep). Bone marrow transplants were more common in the past, but they have largely been replaced by PBSCTs.
Types of transplants
There are 2 main types of stem cell transplants. They differ with regard to the source of the blood-forming stem cells.
Autologous stem cell transplant
In this type of transplant, a patient’s own blood stem cells are removed from his or her bone marrow or peripheral blood. They are collected several times in the weeks before treatment. The cells are frozen and stored while the person gets treatment (high-dose chemotherapy and/or radiation) and then are given back to the patient by infusion into the patient’s blood. This is the more common type of transplant for Hodgkin disease.
Allogeneic stem cell transplant
In this type of transplant, the blood stem cells come from someone else. The donor’s tissue type (also known as the HLA type) needs to match the patient’s tissue type as closely as possible to help prevent the risk of major problems with the transplant.
Usually the donor is a brother or sister if they have the same tissue type as the patient. If there are no siblings who are a good match, the cells may come from an HLA-matched, unrelated donor — a stranger who has volunteered to donate their cells.
Sometimes umbilical cord blood stem cells are used. These cells come from blood drained from the umbilical cord and placenta after a baby is born, which is rich in blood stem cells. These are more often a source of blood stem cells for transplants in children.
Regardless of the source, the stem cells are then frozen and stored until they are needed for the transplant.
Allogeneic transplants may be more likely to rid the body of lymphoma cells, but they are also more likely to cause serious complications that could be life-threatening. In treating Hodgkin disease, an allogeneic transplant is generally used only if an autologous transplant has already been tried without success.
Non-myeloablative transplant: This special type of allogeneic transplant may be an option for some patients who couldn’t tolerate a regular allogeneic transplant because it would be too toxic. This type of transplant uses less chemo and radiation, so it is also known as a mini-transplant or reduced-intensity transplant.
The lower doses of chemotherapy and radiation do not completely destroy the cells in the bone marrow. After treatment, the patient gets the allogeneic (donor) stem cells. These cells establish a new immune system in the body, which sees the lymphoma cells as foreign and attacks them (called the graft-versus-lymphoma effect).
Even though it uses small doses of certain chemotherapy drugs and low doses of total body radiation, this type of transplant can still sometimes work and have less serious side effects. In fact, some patients can receive a non-myeloablative transplant as an outpatient.
Doctors aren’t yet sure exactly how effective these types of transplants are for patients with Hodgkin disease, but studies are now being done to find out.
The transplant procedure
The patient may be admitted to the stem cell transplant unit of the hospital or receive treatment as an outpatient depending on a number of factors.
If they are going to be treated in the hospital, the person is usually admitted to the hospital the day before the high-dose chemo is to begin. He or she will usually stay in the hospital until the stem cells have started to make new blood cells again, which often takes several weeks.
If the transplant is done as an outpatient procedure, patients and families must be able to spot complications requiring their doctor’s attention. Unless they live close to the transplant center, they will be asked to stay in a nearby hotel.
Treatment starts with high-dose chemo and may include high-dose whole body radiation. The chemo and radiation treatments are meant to destroy any remaining cancer cells. They also kill the normal cells of the bone marrow and the immune system. Once treatment is complete, the new stem cells (autologous or allogeneic) are given through a vein, just like a blood transfusion. The stem cells then migrate to the bone marrow.
In an allogeneic SCT, the person getting the transplant may be given drugs to keep the new immune system from attacking the body. This is known as graft-versus-host disease or GVHD. For the next several weeks the patient is likely to have very low blood cell counts, so they are given as much supportive therapy as needed. This may 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 later followed by the new platelet production and new red blood cell production. Because of the high risk of serious infections right after treatment, patients remain protected in isolation (where exposure to germs is kept to a minimum) until a measure of their white blood cells, the absolute neutrophil count (ANC), rises above 500. They can usually leave the hospital when their ANC nears 1,000.
Patients then typically make regular visits to the outpatient transplant clinic for about 6 months, after which their care is continued by their regular doctors. At this point, they may only come back to the clinic for their regular exams or if they have symptoms that should be checked by their doctor.
A stem cell transplant is a complex treatment that can cause life-threatening side effects. 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 stem cell transplant programs may not have experience in certain types of transplants, especially transplants from unrelated donors.
SCTs often require a long hospital stay and can be very expensive (costing well over $100,000). Because some insurance companies may view it as an experimental treatment, they may not pay for it. Even if the transplant is covered by your insurance, your co-pays or other costs could easily amount to tens of thousands of dollars. Find out what your insurer will cover before deciding on a transplant so you will have an idea of what you might have to pay.
Possible side effects
Early or short-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 can be severe. They are caused by damage to the bone marrow and other quickly growing tissues of the body and can include:
- Low blood cell counts (with fatigue and increased risks of infection and bleeding)
- Nausea and vomiting
- Loss of appetite
- Mouth sores
- Hair loss
One of the most common and serious short-term effects is the increased risk for infection. Antibiotics are often given to try to prevent this from happening. Other side effects, like low red blood cell and platelet counts, may require blood product transfusions or other treatments.
Long-term side effects: Some complications and side effects can last for a long time or occur many years after the transplant. These can include:
- Graft-versus-host disease, which occurs only in allogeneic transplants (see next paragraph)
- Menstrual changes, early menopause, and loss of fertility in female patients (caused by damage to the ovaries)
- Loss of fertility in male patients
- Damage to the thyroid gland, causing problems with metabolism
- Cataracts (damage to the lens of the eye that can affect vision)
- Damage to the lungs, causing shortness of breath
- Bone damage called aseptic necrosis (if damage is severe, the patient may need to have part of the affected bone and the joint replaced)
- Development of leukemia or another cancer years later
Graft-versus-host disease (GVHD): This is one of the most serious complications of allogeneic (donor) stem cell transplants. It occurs because the immune system of the patient is replaced by the donor’s immune system. The donor immune system then may “see” the patient’s own body tissues as foreign and may react against them.
Symptoms can include severe skin rashes, itching, mouth sores (which can affect eating), nausea, and severe diarrhea. Liver damage may cause yellowing of the skin and eyes (jaundice). The lungs may also be damaged. The patient may also tire easily and have muscle aches.
GVHD is either acute or chronic, based on how soon after the transplant it begins. Sometimes GVHD can become disabling, and if it is severe enough, it can be life-threatening. Usually, immune-suppressing drugs can be used to help control GVHD, although they can have their own side effects.
On the positive side, the graft-versus-host disease also leads to graft-versus-lymphoma activity. Lymphoma cells remaining after the chemotherapy and radiation therapy are often killed by donor immune cells since the lymphoma cells are seen as foreign by the donor’s immune system as well. Mild graft-versus-host disease can be a good thing.
For more information, see the American Cancer Society document, Stem Cell Transplant (Peripheral Blood, Bone Marrow, and Cord Blood Transplants).
Last Medical Review: 12/10/2012
Last Revised: 01/18/2013