Patient information: Multiple myeloma treatment (Beyond the Basics)
- S Vincent Rajkumar, MD
S Vincent Rajkumar, MD
- Edward W. and Betty Knight Scripps Professor of Medicine
- Mayo Clinic
MULTIPLE MYELOMA OVERVIEW
The treatment of multiple myeloma (MM) is complex because of rapid advances in stem cell transplantation, medications, and better supportive care, which have led to improved survival for patients with multiple myeloma over the past 30 years . The main options for therapy include non-chemotherapy drugs that target the cancer cells, standard chemotherapy drugs, corticosteroids, and stem cell (bone marrow) transplant.
Each option needs to be weighed carefully. Because current therapy is rarely curative, most people go through many treatment regimens during the course of their illness. Stem cell transplantation may not be an option for many people because of advanced age, presence of other serious illness, or other physical limitations (see 'Stem cell transplantation' below).
This topic review discusses the treatment of multiple myeloma. The symptoms, diagnosis, and staging of multiple myeloma are discussed separately. (See "Patient information: Multiple myeloma symptoms, diagnosis, and staging (Beyond the Basics)".)
Types of treatment — There are five main types of treatment:
●Newer drugs — Drugs such as thalidomide (brand name: Thalomid), lenalidomide (brand name: Revlimid), bortezomib (brand name: Velcade), carfilzomib (brand name: Kyprolis), ixazomib (brand name: Ninlaro), and pomalidomide (brand name: Pomalyst) have emerged as important options for treatment of myeloma, both in newly diagnosed patients and in patients with advanced disease who have failed chemotherapy or transplantation. In most cases, these agents are used in combination with dexamethasone, with each other, or with standard chemotherapy agents.
●Chemotherapy — In most people, chemotherapy partially controls multiple myeloma; chemotherapy may lead to complete remission. Chemotherapy drugs used in multiple myeloma include melphalan (brand name: Alkeran), cyclophosphamide (brand name: Cytoxan), Doxorubicin (brand name: Adriamycin), and liposomal doxorubicin (brand name: Doxil).
●Corticosteroids — Corticosteroids include dexamethasone or prednisone.
●Stem cell transplantation — Stem cell transplantation can be done using one's own stem cells (autologous) or using cells from a close relative or matched unrelated donor (allogeneic). In multiple myeloma, most transplants performed are of the autologous kind. Such transplants, although not curative, have been shown to prolong life in selected patients. They can be done as initial therapy in newly diagnosed patients or at the time of relapse. Sometimes, in selected patients more than one transplant may be recommended to adequately control the disease. Autologous transplants for multiple myeloma are very safe in centers with experience in the procedure.
●Immunotherapy — Immunotherapy uses antibodies that target a specific group of cells (usually cancer cells). Elotuzumab (brand name: Empliciti) and daratumumab (brand name: Darzalex) are antibodies that target multiple myeloma cells. They may be used in patients who have progressed despite other therapies.
When to start treatment? — Multiple myeloma can remain stable for prolonged periods of time. Individuals with early myeloma who have no symptoms (often called smoldering myeloma) may be advised to wait months to years before considering chemotherapy.
Individuals with a related condition, called monoclonal gammopathy of undetermined significance (MGUS), do not require treatment, although long-term follow-up is needed; a small percentage of patients with MGUS will eventually develop full-blown myeloma.
However, once symptoms develop, treatment with one or more of the options discussed above is recommended for almost all patients.
Is stem cell transplantation an option? — Because of the risk of toxic and even fatal complications related to stem cell transplantation, not everyone with multiple myeloma is a candidate for stem cell transplantation. Eligibility varies across countries and across institutions. In most European countries, stem cell transplantation for multiple myeloma is offered primarily to patients less than 65 years of age. In the United States, a strict age-limit is not used. Instead, decisions are made on a case-by-case basis based upon a person's health and vary across institutions.
In most centers in the United States, patients with multiple myeloma who have one or more of the following factors are NOT considered eligible for transplantation:
●Age >77 years
●Direct bilirubin >2.0 mg/dL (an elevated bilirubin level indicates that the liver may not tolerate the high dose chemotherapy required before transplantation)
●Serum creatinine >2.5 mg/dL (221 µmol/liter) unless on chronic stable dialysis (creatinine is a reflection of kidney function; those with poor kidney function may not tolerate high dose chemotherapy)
●Eastern Cooperative Oncology Group (ECOG) performance status 3 or 4 unless due to bone pain (table 1)
●New York Heart Association functional status Class III or IV (table 2)
However, these factors are guidelines; the decision regarding transplant eligibility should be made by the patient and physician after discussing the potential risks, benefits, and the needs and wishes of the patient.
TREATMENT OF NEWLY DIAGNOSED MULTIPLE MYELOMA
The initial choice of chemotherapy depends upon the patient's health, age, ability to undergo stem cell transplantation in the future and disease characteristics that denote high, intermediate, or standard risk multiple myeloma . High versus standard risk multiple myeloma is discussed separately. (See "Patient information: Multiple myeloma symptoms, diagnosis, and staging (Beyond the Basics)", section on 'Risk stratification'.)
High risk multiple myeloma treatment options — The best treatment option for patients with high risk multiple myeloma is not clear. Most experts recommend enrolling in a clinical trial (see 'Clinical trials' below).
For patients who are not willing or able to participate in a clinical trial:
●If a person is a candidate for stem cell transplantation, a treatment regimen that includes a proteasome inhibitor such as bortezomib (brand name: Velcade) or carfilzomib (brand name: Kyprolis) is recommended as initial therapy; several studies have suggested that using a regimen that includes a proteasome inhibitor can improve survival in certain subsets of patients with high risk multiple myeloma. Potential regimens include bortezomib, lenalidomide, dexamethasone (VRd) and carfilzomib, lenalidomide, dexamethasone (KRd). After initial therapy (usually about four months), stem cell transplantation either early or later in the treatment course should be considered.
●If a person is not a candidate for stem cell transplantation (because of underlying medical problems, age, or poor health), a regimen that includes a proteasome inhibitor, such as bortezomib, lenalidomide, dexamethasone (VRd) or carfilzomib, lenalidomide, dexamethasone (KRd) is usually recommended as initial therapy. Following initial combination therapy, the proteasome inhibitor is usually continued for an extended time.
●The goal of therapy in high risk myeloma is to achieve and maintain a complete response as much as possible.
Standard or intermediate risk multiple myeloma treatment options — People who have standard or intermediate risk multiple myeloma and who develop symptoms are usually treated with one of the following regimens:
●If a person is a candidate for stem cell transplantation, treatment usually consists of a regimen that does not contain melphalan, such as lenalidomide plus dexamethasone (Rd) or bortezomib, lenalidomide, dexamethasone (VRd). These treatments are less likely to interfere with later collection of stem cells compared with melphalan. (See 'Lenalidomide' below.)
●If a person is not a candidate for stem cell transplantation (because of underlying medical problems, age, or poor health), treatment usually consists of regimens such as lenalidomide plus low dose dexamethasone (Rd) or bortezomib, lenalidomide, dexamethasone (VRd). Melphalan based regimens are less commonly used. If later stem cell transplantation is a possibility, stem cells should be collected before melphalan is given because this drug can cause long-lasting damage to stem cells.
Lenalidomide — Lenalidomide (brand name: Revlimid) is an immune-modulating drug that is effective in the initial treatment of multiple myeloma, usually in combination with dexamethasone. This combination is one of the preferred initial treatment for people with multiple myeloma who are planning to have stem cell transplantation. Both medications are taken as a pill; lenalidomide is taken for 21 of 28 days, along with dexamethasone, which is taken once per week.
The combination of lenalidomide with dexamethasone increases the chance of developing blood clots; an anticoagulant (eg, aspirin or warfarin) is usually recommended to reduce this risk. Lenalidomide has the potential to cause severe birth defects; it is absolutely unsafe (contraindicated) for pregnant women.
Thalidomide (brand name: Thalomid) plus dexamethasone is an alternative to lenalidomide plus dexamethasone, although it may not be as effective and has more toxic side effects. The risks of thalidomide are similar to those of lenalidomide.
Bortezomib — Bortezomib (brand name: Velcade) is a medication that is effective in treating patients with multiple myeloma and other tumors. It is also especially useful in people with kidney failure and those with high-risk multiple myeloma. Bortezomib is given intravenously or subcutaneously, and its main side effects are low blood counts and nerve damage. Bortezomib is typically given in combination with other active drugs. The most commonly used regimen is bortezomib, lenalidomide, and dexamethasone (VRd). Bortezomib is often given once a week under the skin; this approach lowers the risk of nerve damage compared to giving the drug twice a week or by vein.
Treatment-related infections — There is an increased risk of infection during the first two months of chemotherapy or immune modulating therapy. Some of these infections are fatal and, in many cases, they limit the ability to administer chemotherapy. In some centers, daily antibiotics are given during the first two months of chemotherapy to reduce the risk or severity of infections. However, other centers do not routinely recommend preventive antibiotics.
In all cases, vaccination against influenza and pneumonia is strongly recommended before starting chemotherapy. (See "Patient information: Adult vaccines (Beyond the Basics)".)
Plateau phase — Chemotherapy is usually continued until multiple myeloma enters a stable (plateau) phase. The plateau phase is reached when the myeloma becomes stable and shows no signs of progressing. Although this phase is usually temporary, it typically lasts six months or longer. The plateau phase occurs in about one half of individuals after chemotherapy.
Achieving this phase usually requires at least six cycles of treatment, although some people require additional cycles to reach the plateau phase. People with standard risk multiple myeloma do not usually require additional chemotherapy during the plateau phase. However, some physicians recommend maintenance chemotherapy for people with high risk multiple myeloma (see 'High risk multiple myeloma treatment options' above).
A "response" to chemotherapy is defined as a 50 percent reduction in blood and urine levels of the abnormal M protein and an improvement of symptoms.
STEM CELL TRANSPLANTATION
Stem cell transplantation is a treatment option for some individuals with multiple myeloma. There are three types of transplantation, based on the source of the stem cells:
●Autologous transplantation: the stem cells are obtained from the individual with multiple myeloma. This is the type of transplantation that is most commonly recommended.
●Allogeneic transplantation: the stem cells or bone marrow are obtained from a donor with a tissue type matching that of the patient. This type of transplantation carries very high risks and is not recommended for most individuals with multiple myeloma.
●Syngeneic transplantation: the stem cells or bone marrow are obtained from an identical twin of the individual. This is the optimal form of transplantation, although few people with multiple myeloma have an identical twin who can serve as a donor.
Transplantation, when successful, leads to a remission and prolongs survival, and, infrequently, cures multiple myeloma. However, transplantation has several limitations. The high-dose chemotherapy given before transplantation usually fails to kill all of the plasma cells, allowing the condition to relapse after transplantation. Such treatment also puts the patient at risk for serious infections and bleeding, which can be fatal. (See "Patient information: Bone marrow transplantation (stem cell transplantation) (Beyond the Basics)".)
Autologous stem cell transplantation — Autologous stem cell transplantation refers to transplantation with a person's own stem cells. During this procedure, stem cells are collected and frozen for later use. High-dose chemotherapy is then given to kill as many plasma cells as possible, and the stem cells are thawed and returned to the patient. Stem cells obtained from the blood are preferred to stem cells from the bone marrow because blood stem cells take up residence in tissues more quickly and are less likely to be contaminated with cancerous plasma cells.
At present, autologous stem cell transplantation is appropriate for up to 50 percent of people with multiple myeloma. Autologous stem cell transplantation is not recommended for individuals with smoldering myeloma.
Procedure — After initial therapy with a regimen such as lenalidomide/dexamethasone or bortezomib, lenalidomide, dexamethasone (VRd) for three to four months, an individual is given granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF) to stimulate the production of stem cells. If there are not sufficient numbers of stem cells in the blood after G-CSF or GM-CSF, another agent, called Plerixafor, may be added to help with collection. Stem cells are then collected from the blood, frozen, and stored for later use.
After an individual recovers from the stem cell collection, he or she is given high-dose chemotherapy with melphalan (or similar drugs) to kill as many of the malignant plasma cells as possible; then the previously collected stem cells are thawed and returned to the patient. In about one-half of patients, this procedure can be done on an outpatient basis.
Alternatively, after stem cell collection, an individual may be given standard chemotherapy to achieve a plateau phase. At the time of relapse, high doses of melphalan (or similar drugs) are given, and the previously collected stem cells are returned to the patient; this is called delayed transplantation.
Single versus double autologous transplantation — Double autologous transplantation (two consecutive autologous transplantations) may be more effective than single autologous transplantation if the first transplant has not produced a complete or near complete response. The second transplantation is usually performed within six months of the first.
Among individuals undergoing double transplantation, 51 percent have a complete response, lasting, on average, 50 months. One study has shown that double transplantation improves long-term survival relative to single transplantation with the greatest benefit seen in patients who have not achieved an excellent response with the first transplant.
Role of age and stage of myeloma — Because autologous stem cell transplantation has serious side effects, it is generally not recommended for individuals over the age of 70. However, this procedure may be an option for some people over age 70 who are otherwise healthy. The likelihood of a good response to transplantation is somewhat lower for older adults than for younger adults, although the effects of age on survival after transplantation are not completely clear.
Importance of prior treatment — Autologous transplantation is not recommended for people who have received prolonged chemotherapy with alkylating drugs (such as melphalan). This is because it is often difficult to collect a sufficient number of healthy stem cells for transplantation. Other treatments commonly used for multiple myeloma, including thalidomide, bortezomib, and lenalidomide, are safe to take before stem cell transplantation.
Effectiveness — About 1 percent of individuals die from complications related to autologous transplantation. However, compared with chemotherapy alone, autologous stem cell transplantation is more likely to produce a response, and is associated with 12-month longer survival compared to chemotherapy alone (approximately 57 versus 44 months) .
Allogeneic bone marrow transplantation — Allogeneic transplantation requires bone marrow or stem cells from a donor with a matching tissue type. Unfortunately, approximately 25 percent of individuals who undergo allogeneic transplantation die from transplant-related complications, such as infection, lung inflammation, and graft-versus-host disease. Primarily because of this toxicity and the lack of clear benefit, allogeneic transplantation is seldom used for the treatment of myeloma.
Syngeneic transplantation — A syngeneic transplantation refers to a transplantation between identical twins. For individuals who have an identical twin, this treatment option is more effective than either autologous or allogeneic transplantation.
Remission after transplantation — The strict definition of remission requires that there are no signs or symptoms of multiple myeloma and that highly sensitive tests cannot detect any abnormal plasma cells. This type of remission occurs in about 4 percent of individuals after autologous transplantation.
TREATMENT OF MULTIPLE MYELOMA COMPLICATIONS
Multiple myeloma can cause a variety of complications, some of which are life-threatening.
High blood calcium levels — High blood calcium levels develop as bone is lost. Individuals with multiple myeloma should remain as active as possible because physical activity helps counter bone loss.
The treatment of high blood calcium levels usually includes the use of intravenous fluids and prednisone. If this treatment is not effective, treatment with drugs that act against bone loss, such as zoledronic acid (sample brand name: Zometa) or pamidronate (sample brand name: Aredia), a class of drugs called bisphosphonates, may be recommended.
Impaired kidney function — Kidney function becomes impaired in about one half of individuals with multiple myeloma. The treatment of impaired kidney function is aimed at the specific underlying cause.
Treatment usually includes intravenous fluids; it may also include dialysis (a type of blood filtration used for kidney failure), prednisone (a steroid that can indirectly lower blood calcium levels), and allopurinol, a drug that can lower blood levels of uric acid, a waste product from the increased turnover of the malignant plasma cells, which can damage the kidneys.
Patients are advised to stay well-hydrated and should drink enough fluid to produce three liters of urine daily if they have Bence Jones proteinuria (increased light chains in the urine). They should also avoid using any nonsteroidal anti-inflammatory drugs (NSAIDs, such as Advil, Motrin, Aleve) because these drugs might worsen kidney function.
If impaired kidney function has progressed to kidney failure, the treatment options include hemodialysis or peritoneal dialysis. Advanced degrees of kidney failure are usually not reversible even if the multiple myeloma later responds to treatment. (See "Patient information: Dialysis or kidney transplantation — which is right for me? (Beyond the Basics)".)
Infection — Bacterial infections, often indicated by the presence of fever, require prompt treatment with antibiotics. Daily use of the antibiotic trimethoprim-sulfamethoxazole (sample brand names: Bactrim, Septra) can help prevent infections. Individuals who get frequent infections may be advised to take penicillin daily or rarely to have periodic intravenous infusions of gamma globulin.
All individuals with multiple myeloma should receive the pneumococcal vaccine (which reduces the likelihood of pneumonia) and the influenza vaccine (which reduces the likelihood of flu). (See "Patient information: Influenza symptoms and treatment (Beyond the Basics)".)
Bone pain and fractures — Physical activity, with careful avoidance of injury, can promote bone strength in individuals with multiple myeloma. The bone pain associated with multiple myeloma can be controlled with chemotherapy, analgesics (pain relieving drugs), radiation, and bone strengthening drugs such as zoledronic acid (sample brand name: Zometa) or pamidronate (sample brand name: Aredia) (commonly referred to as bisphosphonates) that can also reduce the likelihood of fractures.
In individuals who have early signs of bone erosion, bisphosphonates reduce the risk of fractures and reduce bone pain. Therefore, bisphosphonates are recommended for all individuals who have early signs of bone erosions on x-rays. Bisphosphonates are usually given by intravenous infusion every four weeks; this treatment is continued for approximately two years. These medications may affect kidney function, which should be monitored on a regular basis to avoid this complication.
Dental procedures, such as root canal or extraction of teeth, may be associated with infection or destruction of the jaw (osteonecrosis) in patients treated with intravenous bisphosphonates. Accordingly, patients should avoid such procedures, if possible, while taking these agents; any needed dental procedures should be performed before these agents are started.
Spinal cord compression — Spinal cord compression is a medical emergency that requires prompt treatment to prevent irreversible damage, such as paralysis. Initial treatment may consist of radiation and dexamethasone (a steroid) to reduce swelling around the spinal cord; if these measures are not effective, surgery is needed to relieve pressure on the spinal cord. Patients should call their doctor immediately if they have severe back pain; weakness, numbness, or tingling in the legs; or new problems with control over their bladder or bowel (incontinence).
Anemia — Anemia (low red blood cell count) that is causing symptoms may require blood transfusions or treatment with erythropoietin (EPO), a substance that stimulates the production of red blood cells. Erythropoietin is usually given by injection one to three times per week. This treatment effectively increases levels of hemoglobin (the protein in red blood cells that helps carry oxygen to the tissues), improves symptoms, and reduces the need for blood transfusion.
Thickening of the blood — Thickening of the blood (called hyperviscosity syndrome) rarely occurs in individuals with multiple myeloma. This complication is treated with plasmapheresis, a type of blood filtration that removes the excess monoclonal proteins that cause the thickening.
TREATMENT OF RELAPSED OR REFRACTORY MULTIPLE MYELOMA
Almost all patients with multiple myeloma eventually relapse, and a modest percentage are resistant to initial treatment.
Multiple myeloma that responds poorly or not at all to initial therapy is called refractory multiple myeloma. This condition can occur during the administration of initial chemotherapy or during chemotherapy given after a relapse. Refractory multiple myeloma is more difficult to treat.
●Thalidomide, bortezomib, lenalidomide, carfilzomib, pomalidomide, or ixazomib given with steroids, and/or standard chemotherapy drugs such as melphalan or cyclophosphamide, form the major treatment options for relapsed or resistant disease. These can be used in various combinations depending on the person’s situation; all of these drugs can have side effects. A newer drug, panobinostat, may also be used along with bortezomib and a steroid in certain cases. However, panobinostat is associated with serious side effects, including diarrhea (which may be severe) and cardiac problems. Antibodies that target myeloma cells (elotuzumab or daratumumab) may be incorporated into the treatment of relapsed disease. Other treatment regimens are being studied as well.
●Relapses occurring more than six months after completing chemotherapy are often treated by resuming the initial chemotherapy. Most individuals will again have a response to chemotherapy when it is given a second time, although the response is usually shorter and smaller than the original response. Selected patients can consider autologous stem cell transplantation.
●The lack of response to initial induction chemotherapy does not always mean that the person will not have a good response to autologous stem cell transplantation. Said another way, if a person does not respond to induction chemotherapy, he or she may still respond to autologous stem cell transplantation.
Progress in treating multiple myeloma requires that better treatments be identified through clinical trials. A clinical trial is a carefully controlled way to study the effectiveness of new treatments or new combinations of known therapies; clinical trials are conducted all over the world. Ask for more information about clinical trials, or read about clinical trials at:
Videos addressing common questions about clinical trials are available from the American Society of Clinical Oncology (http://www.cancer.net/pre-act).
WHERE TO GET MORE INFORMATION
Your healthcare provider is the best source of information for questions and concerns related to your medical problem.
This article will be updated as needed on our web site (www.uptodate.com/patients). Related topics for patients, as well as selected articles written for healthcare professionals, are also available. Some of the most relevant are listed below.
Patient level information — UpToDate offers two types of patient education materials.
The Basics — The Basics patient education pieces answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials.
Patient information: Multiple myeloma (The Basics)
Patient information: Monoclonal gammopathy of undetermined significance (The Basics)
Patient information: Neutropenia and fever in people being treated for cancer (The Basics)
Beyond the Basics — Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are best for patients who want in-depth information and are comfortable with some medical jargon.
Patient information: Multiple myeloma symptoms, diagnosis, and staging (Beyond the Basics)
Patient information: Adult vaccines (Beyond the Basics)
Patient information: Bone marrow transplantation (stem cell transplantation) (Beyond the Basics)
Patient information: Dialysis or kidney transplantation — which is right for me? (Beyond the Basics)
Patient information: Influenza symptoms and treatment (Beyond the Basics)
Professional level information — Professional level articles are designed to keep doctors and other health professionals up-to-date on the latest medical findings. These articles are thorough, long, and complex, and they contain multiple references to the research on which they are based. Professional level articles are best for people who are comfortable with a lot of medical terminology and who want to read the same materials their doctors are reading.
Allogeneic hematopoietic cell transplantation in multiple myeloma
Autologous hematopoietic cell transplantation in multiple myeloma
Clinical features, laboratory manifestations, and diagnosis of multiple myeloma
Overview of the management of multiple myeloma
Diagnosis and management of solitary extramedullary plasmacytoma
Diagnosis and management of solitary plasmacytoma of bone
Clinical presentation, laboratory manifestations, and diagnosis of immunoglobulin light chain (AL) amyloidosis (primary amyloidosis)
Evaluating response to treatment of multiple myeloma
Selection of initial chemotherapy for symptomatic multiple myeloma
Management of multiple myeloma in resource-poor settings
Diagnosis of monoclonal gammopathy of undetermined significance
Pathobiology of multiple myeloma
Pathogenesis of immunoglobulin light chain (AL) amyloidosis and light and heavy chain deposition diseases
Pathogenesis and diagnosis of myeloma cast nephropathy (myeloma kidney)
Treatment of relapsed or refractory multiple myeloma
Treatment of kidney disease in multiple myeloma
Treatment of the complications of multiple myeloma
Types of renal disease in multiple myeloma
The use of bisphosphonates in patients with multiple myeloma
The following organizations also provide reliable health information.
●National Library of Medicine
●National Cancer Institute
●American Cancer Society
●The Leukemia & Lymphoma Society
●National Marrow Donor Program
●The American Society of Clinical Oncology
- Kumar SK, Dispenzieri A, Lacy MQ, et al. Continued improvement in survival in multiple myeloma: changes in early mortality and outcomes in older patients. Leukemia 2014; 28:1122.
- Rajkumar SV. Treatment of multiple myeloma. Nat Rev Clin Oncol 2011; 8:479.
- Child JA, Morgan GJ, Davies FE, et al. High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma. N Engl J Med 2003; 348:1875.
- Kyle RA, Rajkumar SV. Multiple myeloma. N Engl J Med 2004; 351:1860.
- Rajkumar SV. Multiple myeloma: 2013 update on diagnosis, risk-stratification, and management. Am J Hematol 2013; 88:226.
- Mikhael JR, Dingli D, Roy V, et al. Management of newly diagnosed symptomatic multiple myeloma: updated Mayo Stratification of Myeloma and Risk-Adapted Therapy (mSMART) consensus guidelines 2013. Mayo Clin Proc 2013; 88:360.
- Palumbo A, Rajkumar SV, San Miguel JF, et al. International Myeloma Working Group consensus statement for the management, treatment, and supportive care of patients with myeloma not eligible for standard autologous stem-cell transplantation. J Clin Oncol 2014; 32:587.
All topics are updated as new information becomes available. Our peer review process typically takes one to six weeks depending on the issue.