2018
DOI: 10.1200/jco.2018.36.15_suppl.7516
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Response rate to lenalidomide plus rituximab (R2) as independent of number of prior lines of therapy: Interim analysis of initial phase of MAGNIFY phase IIIb study of R2 followed by maintenance in relapsed/refractory indolent NHL.

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Cited by 6 publications
(13 citation statements)
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“…Subjects with benefit (at least stable disease) were then randomized to receive maintenance with lenalidomide (10 mg, d1‐21/28 days of cycle) plus rituximab or rituximab alone. Interim results of the postinduction data were presented recently and showed in FL arm with 186 patients a 1‐year rate for PFS of 68% (overall response rate 70%, CR 51%) . The study (NCT01996865) is ongoing.…”
Section: Management Of Flmentioning
confidence: 97%
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“…Subjects with benefit (at least stable disease) were then randomized to receive maintenance with lenalidomide (10 mg, d1‐21/28 days of cycle) plus rituximab or rituximab alone. Interim results of the postinduction data were presented recently and showed in FL arm with 186 patients a 1‐year rate for PFS of 68% (overall response rate 70%, CR 51%) . The study (NCT01996865) is ongoing.…”
Section: Management Of Flmentioning
confidence: 97%
“…Three-year PFS, percent TA B L E 3 FL is classified into the following 3 histologic grades tomography (FDG-PET) showed the potential to upstage approximately 10%-60% of patients with early stages to stages III and IV which subsequently change management of these patients. 17,18 Therefore, FDG-PET is a helpful tool to exclude advance stage prior potential curative treatment in early stages. Furthermore, it can help by determining the most suspected side for transformation to take biopsy.…”
Section: Risk Groupmentioning
confidence: 99%
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“…The MAGNIFY study is a second randomized study in patients with relapsed and refractory FL, marginal zone lymphoma, and mantle cell lymphoma; it compares different durations of lenalidomide therapy and will help clarify the optimal length of lenalidomide therapy. 44 In the RELEVANCE trial, 1030 patients with treatment-naive follicular lymphoma were randomly assigned to either standard chemoimmunotherapy (investigator choice of bendamustine, rituximab [BR], R-CHOP, or rituximab, cyclophosphamide, vincristine, prednisone [R-CVP]) or the combination of lenalidomide and rituximab. Although the trial was designed to demonstrate superiority of the experimental regimen, overall response rates and progressionfree survival were highly similar between the 2 arms.…”
Section: Immunologic Synergymentioning
confidence: 99%
“…Results of the recently reported phase 3 RELEVANCE trial, evaluating R 2 versus R‐chemotherapy in previously untreated advanced FL patients, demonstrated similar efficacy in the two treatment arms, but found a greater frequency of grade 3/4 neutropenia was associated with R‐chemotherapy (Morschhauser et al , ). R 2 immunotherapy has also shown activity in marginal zone lymphoma (MZL), where the combination achieved an overall response rate (ORR) of up to 89% in phase 2 studies (Fowler et al , ; Sacchi et al , ) and is currently being evaluated in the phase 3 MAGNIFY study (Andorsky et al , ).…”
mentioning
confidence: 99%