Small Lymphocytic Lymphoma Clinical Trial
Official title:
A Retrospective Study to Assess the Efficacy and Safety of Chlorambucil Plus Rituximab as Front-line Therapy in Elderly and/or Unfit Patients Affected by B-cell Chronic Lymphocytic Leukemia
This is a non interventional study to evaluate the efficacy and safety of Chlorambucil plus Rituximab as firstline therapy in elderly and/or unfit patients affected by B-cell Chronic Lymphocytic Leukemia (B-CLL).
Illness: treatment overview Chronic lymphocytic leukemia (B-CLL) is the most prevalent adult
leukemia among western countries (6.7% Non-Hodgkin Lymphomas- NHL). The incidence rate is 2-6
cases per 100.000 person per year increasing with age and reaching an incidence rate of about
13/100.000 at 65 years, median age of onset of the disease. There are two clinical staging
systems currently in use for CLL (Rai and Binet staging systems) allowing a rough division of
patients into three prognostic groups: good, intermediate and poor prognosis. The clinical
course ranges from an indolent behaviour (Rai 0, Binet A) with a long term survival to an
aggressive disease with a median survival of 2 years (Rai III and IV, Binet C). There is non
survival benefit associated with an early therapy (Binet stage A and B). Treatment usually is
initiated when patient progress to the advanced stage (Binet stage C) and/or become
symptomatic (fever, night sweats, weight loss). Purine-analogues based chemo-immunotherapy
regimens are now considered the standard of care for fit patient with B-CLL
(Fludarabine-Cyclophosphamyde-Rituximab, FCR regimen). But aging of the host and biological
features of the disease are critical issues in the choice of therapy. The FCR regimen can
result in significant myelosuppression and a high rate of early and late infections,
especially in elderly patients with B-CLL, suggesting that it may be too toxic and therefore
unsuitable for the large subpopulation of elderly and comorbid patients affected by
B-CLL/SLL.
Rationale Chlorambucil, an alkylating agent, was the standard first line treatment for
B-CLL/SLL before the development of the purine analogues and monoclonal antibodies. Later,
phase III trials showed an improved ORR and a prolongation of PFS with fludarabine alone. A
further improvement was obtained with the addition of Cyclophosphamide to Fludarabine.
Eventually, Fludarabine in combination with Cyclophosphamide and the monoclonal anti-CD20
antibody Rituximab became the standard first line therapy for CLL patients 18 to 65 years
old. At the same time, the FCR regimen showed a significant rate of early toxicity consisting
of myelosuppression and infection and also a high rate of late infection. Data showed by
Hallek et al reported a rate of grade 3-4 hematological toxicity and total infections of 56%
and 25%, respectively. They reported 8 treatment-related deaths (2%), five of these due to
infections and 4 deaths occurring before the 3th cycle. Also has been reported by Tam et al a
risk of 10% of late infection for the first year of remission after FCR treatment. Low-dose
FCR was evaluated as an alternative option showing a lower rate of neutropenia, without
reduction of response rate. Nevertheless, it was demonstrated to reduce the PFS and it has
not been evaluated in the elderly or medically unfit population. Alternative treatments
(i.e., low-dose fludarabine, low-dose fludarabine plus cyclophosphamide, rituximab alone)
have been explored in phase II trials in elderly and/or medically unfit patients with CLL.
Since the cohort sizes were small, however, no definitive recommendations could be made for
clinical practice. About three-quarters of CLL patients are more than 65 years old. Data from
the CLL 5 phase III trial of GCLLSG (German CLL study group) comparing fludarabine vs
Chlorambucil in this setting of patients (median age 70 years, range 65-80 years) displayed
no differences in OS and PFR between Fludarabine and Chl, despite a greater percentage of CR
and ORR with Fludarabine. This suggests that in elderly B-CLL patients, Fludarabine alone
does not represent a major benefit in respect of Chl as front-line therapy. However, rates of
complete response (CR) with front-line Chlorambucil single agent are relatively low (up to
7%) as are overall responses (approximately 65%). Phase II trials are ongoing to investigate
the efficacy and safety of Rituximab in combination with Chl in previously untreated patients
affected by B-CLL.
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