2012
DOI: 10.1111/j.1365-2141.2012.09054.x
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Incidence, risk factors and outcome of histological transformation in follicular lymphoma

Abstract: SummaryHistological transformation (HT) into diffuse large B-cell lymphoma (DLBCL) was documented in 37 of the 281 (13%; 95% CI, 9-18) follicular lymphoma (FL) patients treated at our institute from 1979 to 2007. HT occurred at a median of 2·75 years from initial FL diagnosis and HT rate was 15% at 10 years and 26% at 14 years, with a plateau from that point onward. Patients with bulky or extranodal disease, or those diagnosed before 1990 had a significantly higher risk of HT. When initial treatment strategies… Show more

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Cited by 97 publications
(84 citation statements)
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“…18 Survival after transformation was also higher (44% 3-year OS) for the British Columbia patients who transformed after limited-stage FL, 85% of whom were chemotherapy-naive at transformation. 20 Our observation of a median survival of nearly 5 years deserves close scrutiny, but extends the observations that anthracycline-naive patients do relatively well as do patients diagnosed in the era of immunotherapy.…”
Section: Follicular Lymphoma Transformation In the Immunochemotherapymentioning
confidence: 93%
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“…18 Survival after transformation was also higher (44% 3-year OS) for the British Columbia patients who transformed after limited-stage FL, 85% of whom were chemotherapy-naive at transformation. 20 Our observation of a median survival of nearly 5 years deserves close scrutiny, but extends the observations that anthracycline-naive patients do relatively well as do patients diagnosed in the era of immunotherapy.…”
Section: Follicular Lymphoma Transformation In the Immunochemotherapymentioning
confidence: 93%
“…17 Indeed, one recent series of patients diagnosed from 1979 to 2007 found a significantly higher risk of transformation in patients diagnosed before 1990. 18 Similarly, treatment options for management of transformed lymphoma have expanded over this time frame.…”
Section: Journal Of Clinical Oncology O R I G I N a L R E P O R T Volmentioning
confidence: 99%
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“…7 FL is a low grade lymphoma with variable clinical course; in some patients, the disease is indolent and slowly progressive over a period of many years, with waxing and waning lymphadenopathy, whereas in others the disease progresses rapidly, often with transformation to aggressive lymphoma and early death. 8 Despite advances in the treatment of FL, most FL patients remain incurable and, at 5 years approximately 11% 9 to 13% of cases, 10 and at 10 years 15% 10 to 28% 11 of cases will transform to an aggressive phenotype, typically diffuse large B-cell lymphoma (DLBCL). Management strategies include watch and wait, immunochemotherapy, and new targeted treatment options.…”
Section: Introductionmentioning
confidence: 99%
“…27,28 Moreover, in the presence of diffuse areas (425%) of blastic cells in a grade 3 FL, the cases have been proposed to be referred as a full-blown DLBCL. 27,28,35 Also by the molecular point of view, DLBCL includes genetic and molecular alterations often shared with high-grade FL. Both these lymphomas generally express B-cell antigens (CD-19, CD-20, and CD-79a), surface/cytoplasmic immunoglobulin, and (in various proportions) CD10, BCL-2 protein, and BCL-6 protein.…”
Section: Discussionmentioning
confidence: 99%