Grade 3 Follicular Lymphoma: Outcomes in the Rituximab Era |
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Affiliation: | 1. Internal Medicine, Cleveland Clinic, Cleveland, OH;2. Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH;3. Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland, OH;4. Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH;1. Department of Pathology and Laboratory Medicine, Loyola University Healthcare System, Maywood, Illinois;2. Department of Urology, Loyola University Healthcare System, Maywood, Illinois;1. Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan;2. Department of Dermatology, Shinshu University Graduate School of Medicine, Shinshu, Japan;1. Hematology and Marrow Transplant, A.O. SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy;2. Division of Anatomic-Pathology, A.O. SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy;3. Department of Pathology, Center for Experimental Research and Medical Studies, University of Torino, Turin, Italy;4. Divison of Transfusion Medicine, A.O. SS. Antonio e Biagio e Cesare Arrigo, Alessandria, Italy |
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Abstract: | BackgroundFollicular lymphoma (FL) is heterogeneous. Although FL Grade 3B (FL3B) is treated as aggressive FL (aggFL), an optimal approach to FL Grade 3A (FL3A) remains unclear because few data exist on clinical outcomes on the basis of subclassification of FL Grade 3 (FL3) since the introduction of rituximab. We report outcomes of FL3 in the rituximab era.Patients and MethodsWe identified and analyzed a retrospective cohort of 53 patients with FL3A, 3B, and FL Grade 3 with areas of diffuse large B-cell lymphoma (DLBCL). They were divided into 2 groups: aggFL (n = 21) included patients with FL3B (n = 10) and FL3 (A or B) with concomitant DLBCL (n = 11); indolent lymphoma (n = 32) included only FL3A.ResultsBaseline characteristics did not differ between the groups. rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP) was initial treatment in 15 (79%) of patients with aggFL and 21 (72%) of those with FL3A; rituximab was included in initial therapy in 18 (95%) and 24 (83%), respectively. Comparing aggFL and FL3A, 5-year overall survival was 90% versus 79% (P = .97) and 5-year progression-free survival (PFS) 44% versus 34% (P = .75), respectively.ConclusionWe conclude that outcomes for FL3, primarily treated with R-CHOP, do not differ between FL3A and aggFL (FL3B and FL3/DLBCL). The aggFL group showed a plateau in PFS confirming these should be treated with curative intent. FL3A patients, mainly managed with R-CHOP, also show an apparent plateau in PFS. Although longer follow-up and confirmation in other data sets is required, this indicates potential undertreatment of FL3A with less aggressive regimens often used for indolent lymphoma. |
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Keywords: | Aggressive lymphoma Bendamustine Diffuse large B-cell lymphoma Immunochemotherapy Indolent lymphoma |
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