TY - JOUR
T1 - Angioimmunoblastic T-cell lymphoma in Taiwan reveals worse progression-free survival for RHOA G17V mutated subtype
AU - Hsu, Ya Ting
AU - Wang, Yu Chu
AU - Chen, Ruo Yu
AU - Hung, Liang Yi
AU - Li, Sin Syue
AU - Yen, Chi Chieh
AU - Chen, Tsai Yun
AU - Medeiros, L. Jeffrey
AU - Chang, Kung Chao
N1 - Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/4/15
Y1 - 2020/4/15
N2 - Angioimmunoblastic T-cell lymphoma (AITL) carries genetic mutations of TET2, RHOA, and IDH2, but the prognostic impact of these mutations is not widely investigated. Although one study shows no difference in overall survival between patients with or without RHOA G17V mutation, a poor performance status is associated with RHOA G17V-mutated AITL, which is an independent adverse factor. We retrospectively investigated the prognostic impact of RHOA G17V mutation in AITL patients. A total of 31 cases were enrolled (male-to-female, 2.1; mean age: 62.8 years). RHOA G17V mutation was analyzed by deep sequencing. We found that in contrast to RHOA-wild type, patients with RHOA G17V-mutated AITL more frequently had B symptoms (p =.035), stronger PD1 expression (p =.045), ≥3 TFH markers (p =.011), higher blood vessel density (p<.001), and poorer progression-free survival (p =.046). These results support a role for RHOA genetic testing in AITL patients as ROHA G17V mutation carries a worse prognosis, probably associated with B symptoms and stage IV disease.
AB - Angioimmunoblastic T-cell lymphoma (AITL) carries genetic mutations of TET2, RHOA, and IDH2, but the prognostic impact of these mutations is not widely investigated. Although one study shows no difference in overall survival between patients with or without RHOA G17V mutation, a poor performance status is associated with RHOA G17V-mutated AITL, which is an independent adverse factor. We retrospectively investigated the prognostic impact of RHOA G17V mutation in AITL patients. A total of 31 cases were enrolled (male-to-female, 2.1; mean age: 62.8 years). RHOA G17V mutation was analyzed by deep sequencing. We found that in contrast to RHOA-wild type, patients with RHOA G17V-mutated AITL more frequently had B symptoms (p =.035), stronger PD1 expression (p =.045), ≥3 TFH markers (p =.011), higher blood vessel density (p<.001), and poorer progression-free survival (p =.046). These results support a role for RHOA genetic testing in AITL patients as ROHA G17V mutation carries a worse prognosis, probably associated with B symptoms and stage IV disease.
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U2 - 10.1080/10428194.2019.1702179
DO - 10.1080/10428194.2019.1702179
M3 - Article
C2 - 31870198
AN - SCOPUS:85077043755
SN - 1042-8194
VL - 61
SP - 1108
EP - 1118
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 5
ER -