SAN DIEGOThe addition of rituximab (Rituxan) to CHOP
chemotherapy has resulted in a dramatic improvement in outcome for patients of
all ages with diffuse large B-cell (DLBC) lymphoma in a retrospective study
from British Columbia. Improvements were greatest among the elderly population
in the study, Laurie Sehn, MD, clinical assistant professor, British Columbia
Cancer Agency and University of British Columbia, said at the 45th Annual
Meeting of the American Society of Hematology (abstract 88).
She said that in 2000, GELA (Groupe d’Etude des Lymphomes de
l’adult) reported the results of a randomized controlled trial showing improved
outcome with the addition of rituximab to CHOP chemotherapy for elderly
patients with DLBC lymphoma.
"Based on these initial results, the British Columbia Cancer
Agency implemented a new provincial policy on March 1, 2001, recommending the
combination of CHOP and rituximab for all newly diagnosed patients with
advanced-stage DLBC lymphoma," Dr. Sehn said. "We are presenting a
population-based retrospective analysis comparing outcomes over a 3-year
The study ran from September 1, 1999, through August 31,
2002: 18 months prior to (pre-Ritux) and 18 months following (post-Ritux) this
policy change. The cases were identified from three sources: the British
Columbia Provincial Cancer Registry, the British Columbia Cancer pharmacy
records, and the Lymphoma Clinical Database.
Patients were included, Dr. Sehn said, if they were older
than 16 years of age; had a biopsy-proven newly diagnosed DLBC lymphoma; had
clinically advanced-stage disease (stage III-IV; stage I-II with B symptoms or
bulky tumors, or a contraindication to radiation) or testicular DLBC (any
stage); and were treated with an anthracycline-based regimen with curative
Dr. Sehn noted that cases were excluded if they were HIV
positive; had CNS involvement; had evidence of transformation from indolent
lymphoma; were never treated due to frailty, refusal, or rapid clinical
deterioration; or received therapy with only palliative intent.
Researchers identified 294 patients, of whom 142 were pre-Ritux
and 152 were post-Ritux. The patients ranged in age from 19 to 86 (median, 63).
Other patient characteristics included low International
Prognostic Index (IPI) score (24%), low-intermediate IPI score (24%),
high-intermediate IPI score (25%), high IPI score (27%), elevated LDH (65%),
and bulky disease greater than 10 cm (42%).
Dr. Sehn said there were no significant differences in age,
IPI distribution, serum LDH, or presence of bulky disease between the pre-Ritux
and post-Ritux groups.
Although the policy implementation date recommending the use of
rituximab was March 1, 2001, in actuality 9% of patients in the pre-Ritux group
received rituximab with chemotherapy, compared with 85% in the post-Ritux
group. More patients in the pre-Ritux group received radiation therapy (25% vs
15% post-Ritux, P = .04).
The median follow-up for living patients is 34 months for
the pre-Ritux group and 17 months for the post-Ritux group.
Among all patients, 2-year progression-free survival was 52%
pre-Ritux and 71% post-Ritux (P = .0009) (see Figure). Among those aged
60 or older (n = 167), 2-year progression-free survival was 44% pre-Ritux and
73% post-Rutux (P = .0018), compared with 60% and 70%, respectively (P
= .18), for those under age 60 (n = 127).
Two-year overall survival pre- and post-Ritux was 53% and
77%, respectively, for all patients (P = .0001); 40% and 67% for those
age 60 or older (P = .0033), and 69% and 87% for those under age 60 (P
In multivariate analysis controlling for age, IPI score, and B symptoms,
pre-Ritux or post-Ritux treatment remained a strong, independent predictor of
outcome (P = .002).