Weekly x 4 induction therapy with the anti-CD20 antibody rituximab: effect on circulating t(14;18)(+) follicular lymphoma cells

Détails

ID Serval
serval:BIB_46AFDE7A32E5
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Weekly x 4 induction therapy with the anti-CD20 antibody rituximab: effect on circulating t(14;18)(+) follicular lymphoma cells
Périodique
Clinical Lymphoma
Auteur(s)
Pichert  G., Schmitz  S. F., Hess  U., Cerny  T., Cogliatti  S. B., Betticher  D., Stupp  R., Schmitter  D., Stahel  R. A., Ghielmini  M.
ISSN
1526-9655 (Print)
Statut éditorial
Publié
Date de publication
03/2001
Volume
1
Numéro
4
Pages
293-7
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Mar
Résumé
Rituximab 375 mg/m(2) weekly x 4 has been reported to induce a 60% response rate in patients with relapsed follicular lymphomas (FL). Our aim was to examine the effect of this rituximab schedule on circulating FL cells in an ongoing multicenter study. One hundred fifty-four patients with FL were examined by nested polymerase chain reaction (PCR) at baseline for the presence of t(14;18) translocation-carrying lymphoma cells in bone marrow and/or blood. Sixty-four patients (42%) had PCR-detectable t(14;18)(+) FL cells. Pretreatment characteristics of these 64 patients were as follows: one had stage I, nine had stage II, 14 had stage III, and 40 had stage IV disease. Thirty-five patients had bulky disease (> or = 5 cm) and 25 patients had an elevated serum lactate dehydrogenase (LDH) level. Bone marrow was morphologically assessed in 64 patients, and 39 of these patients had an infiltration with FL cells. Blood samples from 51 patients were available for PCR analysis between weeks 8-12 after induction therapy, and 28 of these patients (55%) were PCR negative. Paired blood and bone marrow samples were available for PCR analysis from 39 patients between weeks 8-12 after induction therapy with rituximab. Thirteen of these patients (33%) did not have PCR-detectable cells in blood and bone marrow, while 26 patients (67%) still had circulating t(14;18)(+) cells in either bone marrow (eight patients), blood (one patient), or both (17 patients). PCR negativity in blood and bone marrow in 13 patients was statistically significantly associated with partial or complete response after induction therapy with rituximab (P = 0.006). However, clearance of PCR-detectable t(14;18)(+) cells in bone marrow and/or blood could not be associated with any low tumor burden pretreatment characteristics such as stages I/II, absence of morphological bone marrow infiltration or tumor bulk of > or = 5 cm, and normal serum LDH.
Mots-clé
Adult Aged Aged, 80 and over Antibodies, Monoclonal/*therapeutic use Antigens, CD20/*immunology Antineoplastic Agents/*therapeutic use Chromosomes, Human, Pair 14/*genetics Chromosomes, Human, Pair 18/*genetics Cytogenetic Analysis Drug Administration Schedule Female Humans L-Lactate Dehydrogenase/metabolism Lymphoma, B-Cell/blood/*drug therapy/enzymology/genetics Lymphoma, Follicular/blood/*drug therapy/enzymology/genetics Male Middle Aged Neoplasm Circulating Cells/*drug effects Neoplasm Staging Polymerase Chain Reaction Translocation, Genetic Treatment Outcome
Pubmed
Création de la notice
28/01/2008 9:39
Dernière modification de la notice
20/08/2019 14:52
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