LYON, FranceThe addition of interferon-alfa-2b (IFN,
Intron A) to the usual CHVP regimen (cyclophosphamide, doxorubicin,
teniposide, prednisone) extends survival in elderly patients with
high-risk follicular lymphoma, Dr. Bertrand Coiffier said at the ASH meeting.
He reported results of a randomized GELA study (Groupe dEtude
des Lymphomes de lAdulte) showing longer survival with CHVP
plus interferon than with fludarabine (Fludara). The rationale
for the study, he said, was to try to increase the
efficacy of the chemotherapy by adding interferon.
The study randomized 131 follicular lymphoma patients (all grades) to
receive 12 courses of CHVP plus 18 months of interferon or 12 courses
of fludarabine in 18 months.
Patients were age 60 to 75 years of age, had follicular lymphoma with
a high tumor burden as defined according to the REAL (Revised
European American Lymphoma Study Group) classification, and had at
least one adverse prognostic factor (77% of patients had more than
one poor prognosis factor).
Response Rates and Survival
The response to treatment at 6 months showed a significant difference
in favor of CHVP plus interferon (71% vs 58% in the fludarabine arm).
At 6 months, 21% of the patients receiving combination therapy had
progressed vs 39% on the fludarabine arm.
At 18 months, 57% of CHVP/IFN patients had reached a complete or
partial response vs 39% for fludarabine, and 36% had progressed vs
52% on fludarabine.
At median follow-up of 25 months, time to progression and survival
were significantly shorter in the fludarabine arm than in the
combination arm; 81% of patients receiving CHVP plus interferon were
still alive at 2 years vs 59% on fludarabine.
Multivariate analysis revealed only two factors significantly
associated with survival: treatment and the number of adverse
criteria. Patients who had only one adverse prognostic factor had a
very good survival, compared with those with three or more, Dr.
The CHVP plus interferon regimen appeared to be more toxic: 22
patients stopped interferon, and 8 had a dose reduction because of
adverse events, and 26% of CHVP/IFN patients had grade 3-4
neutropenia vs 5% of fludarabine patients. There was no dose-limiting thrombocytopenia.
The interferon toxicity was more potent than had been described
in the GELA 1986 study, Dr. Coiffier said. But this could have
been because the patients in that earlier study were younger. He said
that 50% of patients on the current study continued treatment with no
problems, and a few had their IFN dosage decreased.
The study confirms the use of CHVP plus interferon as standard
treatment of elderly patients with high-risk follicular lymphoma, Dr.