To report the clinical results after definitive radiotherapy (RT) for indolent primary cutaneous B cell lymphoma (pcBCL). The data concerning all patients treated for indolent pcBCL with RT with a curative intent between 1992 and 2012 were reviewed. All cases were (re)classified according to the World Health Organization (WHO) guidelines. A total of 42 patients with biopsy-proven primary cutaneous follicle center lymphoma (pcFCL) and primary cutaneous marginal zone lymphoma (pcMZL) were included. The median follow-up is 9.5 years. Treatment with RT resulted in complete response (CR) in all patients. Eight patients showed one or multiple relapses confined to the skin. No in-field recurrences were observed. For the entire cohort, the 10-year relapse-free survival (RFS) and overall survival (OS) were 71.1% and 87.1%, respectively. Univariate (UA) and multivariate (MA) analysis revealed extra-trunk primary lesion (MA) and multiple lesions (UA) as unfavorable prognostic factors. The 5-year RFS rate for patients with trunk lesion was 89.4% versus 66.9% for those with other location (p = 0.02). The 5-year RFS rates were 83.5 and 57.1% in case of single and multiple lesions (p = 0.04). An excellent survival can be achieved with definitive RT in indolent pcBCL. Patients with multiple and extra-trunk primary cutaneous lesions probably warrants intensification of therapy. Prospective studies are mandatory.

Radiation therapy in indolent primary cutaneous B cell lymphoma: a single institute experience / De Felice, Francesca; Grapulin, Lavinia; Pieroni, Alessandra; Salerno, Francesca; D’Elia, Gianna Maria; Pulsoni, Alessandro; Musio, Daniela; Tombolini, Vincenzo. - In: ANNALS OF HEMATOLOGY. - ISSN 0939-5555. - 97:12(2018), pp. 2411-2416. [10.1007/s00277-018-3471-x]

Radiation therapy in indolent primary cutaneous B cell lymphoma: a single institute experience

De Felice, Francesca;Pieroni, Alessandra;Salerno, Francesca;Pulsoni, Alessandro;Tombolini, Vincenzo
2018

Abstract

To report the clinical results after definitive radiotherapy (RT) for indolent primary cutaneous B cell lymphoma (pcBCL). The data concerning all patients treated for indolent pcBCL with RT with a curative intent between 1992 and 2012 were reviewed. All cases were (re)classified according to the World Health Organization (WHO) guidelines. A total of 42 patients with biopsy-proven primary cutaneous follicle center lymphoma (pcFCL) and primary cutaneous marginal zone lymphoma (pcMZL) were included. The median follow-up is 9.5 years. Treatment with RT resulted in complete response (CR) in all patients. Eight patients showed one or multiple relapses confined to the skin. No in-field recurrences were observed. For the entire cohort, the 10-year relapse-free survival (RFS) and overall survival (OS) were 71.1% and 87.1%, respectively. Univariate (UA) and multivariate (MA) analysis revealed extra-trunk primary lesion (MA) and multiple lesions (UA) as unfavorable prognostic factors. The 5-year RFS rate for patients with trunk lesion was 89.4% versus 66.9% for those with other location (p = 0.02). The 5-year RFS rates were 83.5 and 57.1% in case of single and multiple lesions (p = 0.04). An excellent survival can be achieved with definitive RT in indolent pcBCL. Patients with multiple and extra-trunk primary cutaneous lesions probably warrants intensification of therapy. Prospective studies are mandatory.
2018
Cutaneous lymphoma; Radiotherapy; Relapse; Response; Skin; Survival; Adult; Aged; Aged, 80 and over; Disease-Free Survival; Female; Follow-Up Studies; Humans; Lymphoma, B-Cell, Marginal Zone; Lymphoma, Follicular; Male; Middle Aged; Retrospective Studies; Risk Factors; Skin Neoplasms; Survival Rate; Hematology
01 Pubblicazione su rivista::01a Articolo in rivista
Radiation therapy in indolent primary cutaneous B cell lymphoma: a single institute experience / De Felice, Francesca; Grapulin, Lavinia; Pieroni, Alessandra; Salerno, Francesca; D’Elia, Gianna Maria; Pulsoni, Alessandro; Musio, Daniela; Tombolini, Vincenzo. - In: ANNALS OF HEMATOLOGY. - ISSN 0939-5555. - 97:12(2018), pp. 2411-2416. [10.1007/s00277-018-3471-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1192561
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