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Contact: Jonathan Weil
Phone: (212) 821-0560
E-mail: jweil@mail.med.cornell.edu
BEXXAR EFFECTIVE AS FIRST-LINE TREATMENT FOR NON-HODGKIN'S LYMPHOMA
PATIENTS WHEN USED WITH CHEMOTHERAPY
New Study Shows Use of Radioimmunotherapy in Combination with Fludarabine
Is Safe and Increases Rate of Complete Response
NEW ORLEANS, LA, December 4, 1999--In a study of previously untreated
patients with low-grade or follicular non-Hodgkin's lymphoma, all patients
achieved a response with Bexxar (tositumomab, iodine I 131 tositumomab)
in combination with fludarabine. The addition of Bexxar to fludarabine
increased the rate of complete response five-fold, as compared to initial
treatment with fludarabine alone, with the rate of complete response continuing
to increase over time. These interim results, the first to report
on the use of a radioimmunotherapy with standard-dose chemotherapy in lymphoma,
were presented today at the 41st annual American Society of Hematology
(ASH) meeting in New Orleans, Louisiana.
"We're extremely excited by these preliminary results which not only
show a high rate of response, but also a dramatic increase in complete
response over time when these low-grade or follicular non-Hodgkin's lymphoma
patients are treated with the sequential combination of Bexxar following
fludarabine," said John P. Leonard, M.D., assistant professor of medicine
in the division of hematology and medical oncology at the Weill Medical
College of Cornell University. "Bexxar not only demonstrates durable
responses as a stand-alone first-line treatment in previously untreated
patients and in those whoíve relapsed or become refractory, but
now shows clinical potential when used in conjunction with conventional
chemotherapy as an initial treatment regimen."
Interim Data Shows Promising Results
Conducted at the Center for Lymphoma and Myeloma at the Weill Medical
College of Cornell University and New York-Presbyterian Hospital, this
Phase II study enrolled 38 patients with previously untreated low-grade
or follicular non-Hodgkin's lymphoma (NHL). The study was designed
to evaluate the safety and efficacy of a sequential regimen of fludarabine
followed by tositumomab, iodine I 131 tositumomab. Patients received
three cycles of fludarabine (25 mg/m2 x 5 d every 5 weeks) followed six
to eight weeks later by tositumomab, iodine I 131 tositumomab.
Fourteen of the 38 patients were evaluable for response at least six
months after treatment with tositumomab, iodine I 131 tositumomab.
Ninety-three percent of patients (13 out of 14) had Stage IV NHL at the
time of treatment; one patient had Stage II NHL. All of the patients
in the study achieved a response to treatment with fludarabine followed
by tositumomab, iodine I 131 tositumomab. With the addition of tositumomab,
iodine I 131 tositumomab, after six months of follow-up, the rate of complete
response (elimination of the signs and symptoms of the disease) increased
five-fold as compared to initial treatment with fludarabine. Following
initial treatment with fludarabine, 14 percent of patients (two out of
14) experienced a complete response. At the thirteenth week, following
treatment with tositumomab, iodine I 131 tositumomab, the rate of complete
response increased to 43 percent (six out of 14 patients).
At approximately six months, 71 percent of patients (10 out of 14) had
experienced a complete response. Multicenter studies using tositumomab,
iodine I 131 tositumomab in combination with fludarabine are scheduled
to begin next year.
Treatment with fludarabine in combination with tositumomab, iodine I
131 tositumomab was well tolerated. The principal side effects were
hematologic, including a decrease in blood counts, which was reversible.
Non-hematologic side effects experienced with tositumomab, iodine I 131
tositumomab were mild-to-moderate, including nausea, fatigue, headache
and rhinitis. Due to the immunosuppressive effect of fludarabine,
only one patient developed human anti-mouse antibodies (HAMA).
"Helping patients achieve long, durable complete responses is our best
hope until we find a cure for low-grade non-Hodgkin's lymphoma.
This study suggests that use of Bexxar with chemotherapy is a promising,
well-tolerated combination that may offer this patient population a much-needed
new treatment option," said Dr. Leonard.
Tositumomab, iodine I 131 tositumomab is a novel radioimmunotherapy
consisting of a radioisotope (iodine 131) combined with a monoclonal antibody.
The monoclonal antibody attaches to a protein found only on the surface
of B-cells, inhibiting tumor cells directly and/or recruiting the immune
system to kill these cells. Simultaneously, a radioisotope delivers
targeted, powerful radiation to destroy the cancer. As a result,
the tumor cells receive a greater concentration of the therapeutic radiation
while radiation to normal tissues is minimized.
Non-Hodgkin's Lymphoma
Non-Hodgkin's lymphoma (NHL) is a form of cancer that affects the blood
and lymphatic tissues. The fifth leading cause of death among cancers
in the United States, NHL also has the second fastest growing mortality
rate. According to the National Cancer Institute, nearly 300,000
people are afflicted with NHL in the United States alone. Currently,
there is no cure for advanced stage low-grade NHL. In more than 40
years, there have been no changes in the survival rates of low-grade NHL
patients, who typically die from the disease or complications associated
with current treatments.
Founded in 1898, Cornell University Medical College (now known as Joan
and Sanford I. Weill Medical College of Cornell University) has long ranked
among the leading medical schools in the U.S. From the start, the
medical college has followed an educational philosophy that emphasizes
the importance of combining a strong basic foundation in the medical sciences
with extensive clinical training in patient care. In 1927, the Medical
College and The New York Hospital (now New York-Presbyterian Hospital)
entered into a major affiliation agreement, which culminated with the opening,
in 1932, of a unified campus on the Upper East Side of Manhattan.
Cornell physicians and scientists are engaged in both basic and clinical
research in the cutting-edge areas of genetics and gene therapy, neuroscience,
structural biology, AIDS, cancer, and psychiatry, among others. Cornell's
biomedical investigators are delving ever deeper into the realms of cellular
and molecular biology, which hold the secrets both to the normal functioning
of the body and the malfunctions that lead to serious medical disorders.
© 1999 New York Presbyterian
Hospital
Weill Medical College of Cornell
University
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