|
|
Phase
II trial of high-dose chemotherapy with autologous stem cell transplantation in
first-line therapy of primary central nervous system (CNS) lymphoma
P.
Colombat, T. Lamy, A. Lemevel, V. Delwail, M. Gardembas, A. Brion, C. Berthou,
J.-O. Bay, R. Delepine, C. Linassier
for
the Goelams Study Group; CHU Bretonneau, Tours, France; CHU Pontchaillou, Rennes,
France; Centre Rene Gauducheau, Nantes, France; CHU la Mileterie, Poitiers,
France; CHU, Angers, France; CHU, Besancon, France; CHU, Brest, France; Centre
Jean Perrin, Clermont-Ferrand, France
Introduction.
The prognosis of primary CNS lymphoma remains poor with conventional
chemotherapy and radiotherapy.
High-dose chemotherapy (HDT) with autologous blood stem cell transplantation (ASCT)
has given encouraging results as salvage treatment.
We conducted a phase II study between July 99 and November 2001 to evaluate the
efficacy of HDT in the first-line treatment of primary CNS.
Patients
and Methods.
Eligible criteria were histologically proven lymphoma, age
£
60 years, no immunodeficiency, adequate liver, renal, lung and hematopoietic
function.
Patients (pts) received 2 courses of MVBP (Methotrexate 3 g/m2/d
d1,5), VP16 100 mg/m2 on d2, BCNU 100 mg/m2 on d3,
methylprednisolone 60 mg/m2/day, d1-5) and intrathecal prophylaxis;
patients in complete or partial remission, had peripheral blood stem cells
collection after ifosfamide (1,5 g/m2 on d1-3) and cytarabine (2 g/m2/day
on d1-2); HDT with BEAM (BCNU 300 mg/m2 d1, VP16 400 mg/m2/d
d2-5, cytarabine 200 mg/m2/d d2-5 and melphalan 140 mg/m2
d6) was supported by ASCT; after transplantation, patients had whole brain
irradiation at a dose of 30 Gy, 1.8 Gy/fr.
Results.
25 patients, 9 men and 16 women, were included.
Median age was 51 years (21-60).
All patients had diffuse large cell lymphoma.
ECOG performance status was 0 in 3 pts, 1 in 10 pts, 2 in 4 pts, 3 in 6 pts and
4 in 2 pts.
Twelve patients had a unique site and 13 had multifocal presentation.
Serum LDH level was increased in 6 pts.
HDT with BEAM was performed in 16 pts (4 progressions, 3 toxicities and 2
refusals).
One toxic death occured among the 16 pts treated with BEAM.
With a median follow-up time of 24.6 months (13-43), the probability of overall
survival at 36 months was 55% for the whole population, 90% for patients who
received BEAM intensive chemotherapy and 0% for pts who were not intensified.
Conclusion.
High-dose chemotherapy with autologous blood stem cell transplantation is
feasible and resulted in a high rate of disease control.
A longer follow is necessary but a randomized comparison with conventional
chemotherapy including high-dose methotrexate is necessary.
© Copyright 2003 American Society of Clinical Oncology. All rights
reserved worldwide
Source: http://www.asco.org/ac/1,1003,_12-002489-00_18-002003-00_19-00103220-00_29-00A,00.asp?cat=CNS+Tumors&parent=
Central+Nervous+System+Tumors&returnpid=2325&SubCat_ID=4
|