Clinicopathologic correlations of stage IE/IIE primary thyroid diffuse large B-cell lymphoma

Background: We studied the clinicopathological characteristics and prognoses of localized stage thyroid diffuse large B-cell lymphoma (DLBCL). Patients and methods: This study included 32 patients with stage I/IIE thyroid DLBCL. Their median age was 66 years, the male/female ratio was 10/22. Results...

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Bibliographic Details
Published inAnnals of oncology Vol. 18; no. 7; pp. 1203 - 1208
Main Authors Niitsu, N, Okamoto, M, Nakamura, N, Nakamine, H, Bessho, M, Hirano, M
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.07.2007
Oxford Publishing Limited (England)
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Summary:Background: We studied the clinicopathological characteristics and prognoses of localized stage thyroid diffuse large B-cell lymphoma (DLBCL). Patients and methods: This study included 32 patients with stage I/IIE thyroid DLBCL. Their median age was 66 years, the male/female ratio was 10/22. Results: As to the cellular immunophenotype, CD20 was positive in 31/32, CD5 in 0/32, CD10 in 4/32, CD23 in 1/32, BCL2 in 14/30, and BCL6 in 24/32. Twelve cases showed abnormal karyotypes: two cases with t(8;14)(q24;q32), four cases with 3q27, two cases with 17p11, and four cases with other abnormal karyotypes. As for treatment, eight cases were treated with chemotherapy alone and 24 cases were treated with chemotherapy followed by radiotherapy. Complete response was achieved in 94%. The 5-year progression-free survival was 84% and the 5-year overall survival was 90% with a median follow-up period of 62 months. The germinal center B-cell (GCB) type had a significantly better prognosis than the non-GCB type. Conclusion: Localized stage thyroid DLBCL is a disease with a relatively good prognosis. It is, however, a heterogeneous disease with regard to histological type and pathological state. Localized stage thyroid DLBCL has a good prognosis and it is that there are more GCB-type DLBCL lymphomas.
Bibliography:istex:22E0B852683C7F2572A27F6F57ACAF50391F52C7
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ISSN:0923-7534
1569-8041
DOI:10.1093/annonc/mdm094