History & Overview Annual Report President's Pages Center News Community Affairs
Make a Gift Yankees Universe Fund Fred's Team Donating Blood & Platelets Volunteering Thrift Shop Park Avenue Potluck Cookbook
Press Releases Information for Journalists News@MSKCC
Manhattan New Jersey Long Island Westchester
Working at Memorial Sloan-Kettering Work Sites College Recruitment About Nursing Job Fairs & Career Days Job Search & Apply Online
Making an Appointment
Our Publications
Our Publications
Visit PubMed for our journal articles

At Memorial Sloan-Kettering, our doctors take a multidisciplinary team approach to multiple myeloma and related diseases, drawing on the expertise of hematologic oncologists, radiation oncologists, radiologists, pathologists, bone marrow transplant specialists, and pain specialists who collaborate closely on each patient's care.

Team members use state-of-the-art diagnostic tools to help determine the most effective course of treatment for each patient. Memorial Sloan-Kettering specialists treat more than 200 new patients each year with multiple myeloma and other plasma-cell diseases -- making ours one of the largest programs of its kind in the United States. Learn more about our multidisciplinary team approach to care and some of our areas of focus and expertise below.

New Therapies

Thalidomide, a medicine first used in the late 1950s as a sleeping pill and to combat the nausea some women experience in the first trimester of pregnancy, was found to cause birth defects and was later banned. In the late 1990s, cancer researchers discovered that thalidomide is an effective treatment for myeloma throughout the course of the disease as both first-line and maintenance treatment. It is also given to patients whose disease has relapsed.

Our Clinical Trials
Our Clinical Trials
Find out about new research studies for multiple myeloma

Through clinical trials, Memorial Sloan-Kettering investigators showed that nearly 90 percent of patients with myeloma responded to a combination of thalidomide plus dexamethasone when administered following a regimen of dexamethasone combined with the chemotherapy drug doxorubicin. Dexamethasone is a medication used to counteract certain side effects of chemotherapeutic treatment. Patients show a high response rate when dexamethasone is combined with thalidomide, although the combination can sometimes cause side effects. These include blood clots and a serious skin disorder called toxic epidermal necrosis. However, we have found that a majority of patients are able to tolerate the treatment.

We also use a new blood test -- a serum-free light-chain assay -- which can predict the likelihood a patient will achieve a complete, or near-complete, response to therapy.

Our researchers have also shown that bortezomib (Velcade®) the first in a new class of medicines called proteasome inhibitors and the first new treatment in more than a decade to be approved for multiple myeloma is effective in newly diagnosed myeloma patients.

About Transplantation
About Transplantation
Information for those facing stem cell transplantation

Stem Cell Transplantation

At Memorial Sloan-Kettering, we are committed to improving the outcomes of patients who undergo stem cell transplantation for the treatment of multiple myeloma. On average, patients who receive a stem cell transplant at our hospital do extremely well. (More than 99 percent of myeloma patients who receive transplants at Memorial Sloan-Kettering survive the most dangerous period following the procedure, which is the first 100 days.) In addition, we have developed new growth factors and other medications to increase the number of stem cells that are available for collection.

Researchers are not only testing new treatments but are developing diagnostic tools such as microarray analysis, a DNA test that analyzes the expression of thousands of genes and can profile an individual's cancer to determine the treatment to which each patient is most likely to respond.

Expertise in Amyloidosis

Primary amyloidosis (AL) is a condition in which abnormal plasma cells produce a light-chain protein (M protein), a part of an antibody that collects in organs such as the kidney, heart, liver, and nerves and interferes with their normal function. About 10 to 15 percent of patients with myeloma will either have or develop amyloidosis. We treat amyloidosis with a combination of chemotherapy and stem cell transplantation.

AL amyloidosis is sometimes confused with familial amyloidosis at diagnosis. By using additional screening procedures, Memorial Sloan-Kettering physicians ensure that patients are correctly diagnosed and treated.

Our physicians have special expertise in treating amyloidosis, particularly when it involves the heart. We collaborate with other New York City hospitals that provide heart transplants to selected patients with amyloidosis. We also have an excellent record of success using stem cell transplants to treat these patients; many do well despite sometimes irreversible heart damage. Our AL patients with damage in the kidney, liver, gastrointestinal tract, or peripheral nervous system usually improve following treatment that includes a stem cell transplant.

We also pioneered a treatment program combining autologous stem cell transplantation with the drug melphalan. This approach markedly reduces or eliminates the problematic protein in most AL patients who receive this treatment. We are currently studying ways to further increase stem cell mobilization and to improve the overall care of patients who undergo autologous stem cell transplantation.

  • Other Plasma-Cell Diseases
    Memorial Sloan-Kettering also treats patients with related plasma-cell diseases. These diseases include systemic light-chain amyloidosis (AL), a rare and often fatal disease, and less serious disease conditions, such as solitary plasmacytoma and monoclonal gammopathy of undetermined significance (MGUS).

Last Updated: Sep. 27, 2006
PrintEmail This Page