Angioimmunoblastic T-cell lymphoma in Taiwan shows a frequent gain of ITK gene

Peir In Liang, Sheng Tsung Chang, Ming Yen Lin, Yen Chuan Hsieh, Pei Yi Chu, Chih Jung Chen, Kai Jen Lin, Yun Chih Jung, Wei Shou Hwang, Wen Tsung Huang, Wei Chin Chang, Hongtao Ye, Shih Sung Chuang

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17 Citations (Scopus)

Abstract

Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive peripheral T-cell lymphoma (PTCL) of follicular helper T-cell origin and is rare in Taiwan. There are overlapping features of AITL and peripheral T-cell lymphoma with a follicular growth pattern (PTCL-F). Around one fifth of PTCL-F exhibits t (5; 9) (q33; q22)/ITK-SYK chromosomal translocation, which is essentially absent in AITL. We retrospectively investigated 35 cases of AITL from Taiwan with histopathology review, immunohistochemistry, in situ hybridization for Epstein-Barr virus (EBV) and fluorescence in situ hybridization (FISH) for t(5;9)(q33;q22)/ITK-SYK and correlated the results with overall survival. Twenty-six cases of not otherwise specified PTCL (PTCL-NOS) were also examined by FISH for comparison. Most AITL patients were male (69%) and elderly (median age at 67 years) with frequent bone marrow involvement (53%), high Ann Arbor stages (77%), and elevated serum lactate dehydrogenase (68%). Most cases (80%) showed a typical CD4+/CD8- phenotype and in 90% cases there were scattered EBV-positive B-cells (less than 10% cells). None of these cases showed t(5;9)(q33;q22)/ITK-SYK translocation by FISH. Gain of ITK and SYK gene was identified in 38% and 14% tumors, respectively, but both were not associated with overall survival. Performance status < 2 was associated with a better outcome but not the other clinicopathological factors. All PTCL-NOS cases were negative for ITK-SYK translocation with similar rates (38% and 12%, respectively) of gains at ITK and SYK loci as that of AITL. In this so far the largest series of AITL from Taiwan, we reported the clinicopathological features and FISH findings on ITK and SYK genes. We confirmed the absence of t(5;9)(q33;q22)/ITK-SYK translocation, which may serve as an additional differential diagnostic tool from PTCL-F when present. PTCL-NOS shared a similar pattern of ITK and SYK gains with AITL. More studies are warranted to elucidate the roles of SYK and ITK and other genes in the lymphomagenesis of AITL in Taiwan.

Original languageEnglish
Pages (from-to)6097-6107
Number of pages11
JournalInternational Journal of Clinical and Experimental Pathology
Volume7
Issue number9
Publication statusPublished - 2014
Externally publishedYes

Keywords

  • Angioimmunoblastic T-cell lymphoma
  • Follicular helper T-cell
  • Follicular T-cell lymphoma
  • ITK
  • Peripheral T-cell lymphoma
  • SYK
  • Taiwan

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Histology

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