Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2001-1-22
pubmed:abstractText
The clinical activity of rituximab, a chimeric monoclonal antibody which binds to the CD20 antigen, was evaluated as a single first-line therapy for patients with follicular non-Hodgkin lymphoma (NHL). Fifty patients with follicular CD20(+) NHL and a low tumor burden were analyzed for clinical and molecular responses. They received 4 weekly infusions of rituximab at a dose of 375 mg/m(2). The response rate a month after treatment (day 50) was 36 of 49 (73%), with 10 patients in complete remission, 3 patients in complete remission/unconfirmed, and 23 patients in partial remission. Ten patients had stable disease, and the disease progressed in 3 patients. One of 13 (8%) patients in complete remission, 9 of 23 (39%) patients in partial remission, and 5 of 10 (50%) patients with stable disease exhibited disease progression during the first year. Within the study population, 32 patients were initially informative for polymerase chain reaction (PCR) data on bcl-2-J(H) rearrangement. On day 50, 17 of 30 patients (57%) were negative for bcl-2-J(H) rearrangement in peripheral blood, and 9 of 29 (31%) were negative in bone marrow; a significant association was observed between molecular and clinical responses (P <.0001). At month 12, 16 of 26 patients (62%) were PCR negative in peripheral blood. These results indicate that early molecular responses can be sustained for up to 12 months and that this response is highly correlated with progression-free survival. Rituximab has a high clinical activity and a low toxicity and induces a high complete molecular response rate in patients with follicular lymphoma and a low tumor burden.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
97
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
101-6
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:11133748-Adolescent, pubmed-meshheading:11133748-Adult, pubmed-meshheading:11133748-Aged, pubmed-meshheading:11133748-Antibodies, Monoclonal, pubmed-meshheading:11133748-Antibodies, Monoclonal, Murine-Derived, pubmed-meshheading:11133748-Antigens, CD20, pubmed-meshheading:11133748-Antineoplastic Agents, pubmed-meshheading:11133748-Disease Progression, pubmed-meshheading:11133748-Female, pubmed-meshheading:11133748-Follow-Up Studies, pubmed-meshheading:11133748-Gene Rearrangement, pubmed-meshheading:11133748-Genes, bcl-2, pubmed-meshheading:11133748-Humans, pubmed-meshheading:11133748-Immunoglobulin Joining Region, pubmed-meshheading:11133748-Lymphoma, Follicular, pubmed-meshheading:11133748-Male, pubmed-meshheading:11133748-Middle Aged, pubmed-meshheading:11133748-Polymerase Chain Reaction, pubmed-meshheading:11133748-Remission Induction, pubmed-meshheading:11133748-Time Factors, pubmed-meshheading:11133748-Treatment Outcome
pubmed:year
2001
pubmed:articleTitle
Rituximab (anti-CD20 monoclonal antibody) as single first-line therapy for patients with follicular lymphoma with a low tumor burden: clinical and molecular evaluation.
pubmed:affiliation
CHU Bretonneau, Tours, France.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, Non-U.S. Gov't, Multicenter Study