Annals of Oncology Advance Access published online on October 30, 2006
Annals of Oncology, doi:10.1093/annonc/mdl395
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1 Service des Maladies du Sang, Lille, France
* To whom correspondence should be addressed. Single-agent gemcitabine has shown encouraging results in patients with mantle cell lymphoma (MCL). This phase II study further explored the potential of a gemcitabine-based regimen in patients with relapsed or refractory MCL. Patients <70 years old received the PDG regimen: gemcitabine (1000 mg/m2, days 1 and 8), dexamethasone (40 mg/m2, days 1-4), and cisplatin (100 mg/m2, day 1). Patients
Received June 13, 2006
Revised September 6, 2006
Accepted September 14, 2006
original article
Phase II study of gemcitabine-dexamethasone with or without cisplatin in relapsed or refractory mantle cell lymphoma
F. Morschhauser 1, S. Depil 1, E. Jourdan 2, M. Wetterwald 3, R. Bouabdallah 4, G. Marit 5, P. Solal-Céligny 6, C. Sebban 7, B. Coiffier 8, N. Chouaki 9, F. Bauters 1, and C. Dumontet 8 *
2 Service d'Hématologie, Nîmes, France
3 Service d'Hématologie, Dunkerque, France
4 Service d'Hématologie, Marseille, France
5 Service des Maladies du Sang, Bordeaux, France
6 Service Oncologie-Maladies du Sang, Le Mans, France
7 Centre Léon Bérard, Lyon, France
8 Service d'Hématologie, Pierre Bénite, France
9 Eli Lilly, Paris, France
C. Dumontet, E-mail: charles.dumontet{at}chu-lyon.fr
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Abstract
70 years of age received dexamethasone and gemcitabine only (DG regimen). Thirty patients (12 in the DG group, 18 in the PDG group) with a median age 66.5 years (range, 47-81) received a median of six cycles in both groups. The overall response rate was 36.4% [95% confidence interval (CI), 15.2% to 64.6%] with the DG regimen and 44.4% (95% CI 24.6% to 66.3%) with the PDG regimen. The median progression-free survival was 3 months (95% CI 0.0-7.9) in the DG group and 8.5 months (95% CI 4.8-12.2) in the PDG group. With a median follow-up of 38.8 months, 13 patients (including 11 given PDG) are still alive. DG was well tolerated, and thrombocytopenia was the most prevalent toxicity in patients receiving PDG. Both regimens deserve to be further investigated as a backbone for combination chemotherapy in patients with MCL.![]()
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