H O U S T O N - A d d i n g rituximab(Drug information on rituximab) (Rituxan) to fludarabine
(Fludara)/cyclophosphamide
(Cytoxan, Neosar) (FCR) prolongs
survival in patients with relapsed
chronic lymphocytic leukemia
(CLL), according to Guillermo
Garcia-Manero, MD. Dr. Garcia-
Manero is assistant professor in the
Department of Leukemia at The
University of Texas M. D. Anderson
Cancer Center in Houston. He
presented updated data on this
study in a poster at the 43rd Annual
Meeting of the American Society of
Hematology (abstract 2650).
During course 1, rituximab was
given at a slow rate at 375 mg/m2
on day 1 followed by fludarabine at
25 mg/m2 and cyclophosphamide(Drug information on cyclophosphamide)
at 250 mg/m2 on days 2-4. During
subsequent courses (2-6),
rituximab was given at 500 mg/m2
on day 1 and fludarabine and cyclophosphamide,
which were given
at the same doses, were given on
days 1-3.
Data on Previously Treated
CLL Patients
Dr. Garcia-Manero presented
data on 136 patients with previously
treated CLL. These included 4 with
Rai stage 0, 35 with stage I, 26 with
stage II, 19 with stage III, and 52
with stage IV disease. Patients had a
median of 2.5 previous treatments
(range: 1-10). Median platelet count
at baseline was 116.5 x 109/L (range:
6-388 x 109/L); median hemoglobin
was 12.1 g/dL (range: 6.8-16.5
g/dL); and median white blood
count was 51.9 x 109/L (range: 1.3-
583 x 109/L). Sixty percent of patients
had three or more lymph node
sites involved.
Using National Cancer Institute
(NCI) criteria, Dr. Garcia-Manero
reported 28 (21%) complete responses
(CR), 18 (13%) nodular
partial responses (nPR), and 50
(37%) partial responses (PR), for
an overall response rate (ORR) of
71%. Five of 14 patients (35%) who
had immunoglobulin rearrangements
detectable by polymerase
chain reaction (PCR) assay at study
entry had molecular complete responses
(PCR negative) after treatment.
Responses varied depending
on prior therapy (see Table 1).
Rituximab Combination
Prolongs Survival
Compared to historical data on
CLL patients treated with
fludarabine/cyclophosphamide, the
FCR combination prolonged survival
(see Figure 1). Adding
rituximab increased not only the
ORR but the proportion of those
responses that were complete remissions,
according to Dr. Garcia-
Manero.
Frequent toxicities related to
rituximab included chills and fever.
Others were nausea/vomiting, hypotension,
and dyspnea. Serious
toxicities included eight episodes of
pneumonia, seven episodes of neutropenic
fever, five of sepsis, and
one prolonged myelosuppression.
"In summary, the combination
of fludarabine, cyclophosphamide,
and rituximab is a very active program
for patients with previously
treated CLL," Dr. Garcia-Manero
said.
