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Clinicopathologic analysis of nodal T-follicular helper cell lymphomas, a multicenter retrospective study from China.
Ma, Shanshan; Li, Suxiao; Zuo, Xiaona; Li, Wencai; Wang, Lifu; Liu, Weiping; Wang, Zhe; Sang, Wei; Wang, Yanjie; Zhang, Xudong; Zhang, Mingzhi.
Afiliação
  • Ma S; Department of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Li S; Department of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zuo X; Department of Pathology, Beijing Boren Hospital, Beijing, China.
  • Li W; Department of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Wang L; Department of Pathology, Henan Province People's Hospital, Zhengzhou, China.
  • Liu W; Department of Pathology, Department of Pathology, West China Hospital of Sichuan University, Chengdu, China.
  • Wang Z; Department of Pathology, Department of Pathology, Xijing Hospital, the Fourth Military Medical University, Xi'an, China.
  • Sang W; Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Wang Y; Department of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zhang X; Department of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zhang M; Department of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Front Immunol ; 15: 1371534, 2024.
Article em En | MEDLINE | ID: mdl-38601148
ABSTRACT

Background:

Nodal T-follicular helper cell lymphomas (nTFHLs) represent a new family of peripheral T-cell lymphomas (PTCLs), and comparative studies of their constituents are rare.

Methods:

This study retrospectively enrolled 10 patients with nTFHL-F and 30 patients with nTFHL-NOS diagnosed between December 2017 and October 2023 at six large comprehensive tertiary hospitals; 188 patients with nTFHL-AI were diagnosed during the same period at the First Affiliated Hospital of Zhengzhou University for comparison.

Results:

Compared with nTFHL-AI, nTFHL-NOS patients exhibited better clinical manifestations, lower TFH expression levels, and a lower Ki-67 index. However, no differences in clinicopathological features were observed between nTFHL-F and nTFHL-AI patients as well as nTFHL-NOS patients. According to the survival analysis, the median OS for patients with nTFHL-NOS, nTFHL-AI, and nTFHL-F were 14.2 months, 10 months, and 5 months, respectively, whereas the median TTP were 14 months, 5 months, and 3 months, respectively. Statistical analysis revealed differences in TTP among the three subtypes(P=0.0173). Among the population of patients receiving CHOP-like induction therapy, there were significant differences in the OS and TTP among the nTFHL-NOS, nTFHL-AI, and nTFHL-F patients (P=0.0134, P=0.0205). Both the GDPT and C-PET regimens significantly improved the ORR, OS, and PFS in nTFHL patients.

Conclusion:

There are significant differences in the clinical manifestations, pathology, and survival outcomes among the three subtypes of nTFHLs. However, further research with a larger sample size, and involving clinical pathology and molecular genetics is needed to determine the distinctive biological characteristics of these tumors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma de Células T Periférico Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma de Células T Periférico Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2024 Tipo de documento: Article