Cytotoxic T-lymphocyte-associated 4 protein expression is associated with a high international prognostic score in advanced-stage classical Hodgkin lymphoma

被引:1
|
作者
Pangaribuan, Flora Dameria [1 ]
Ham, Maria Francisca [2 ,3 ]
Mutmainnah, Mutiah [4 ]
Harahap, Agnes Stephanie [2 ,3 ]
机构
[1] Persahabatan Hosp, Anat Pathol Dept, Dept Anat Pathol, Jakarta 13230, Indonesia
[2] Univ Indonesia, Dr Cipto Mangunkusumo Natl Cent Gen Hosp, Fac Med, Dept Parasitol,Anat Pathol Dept, Jakarta 10430, Indonesia
[3] Univ Indonesia, Fac Med, Human Canc Res Ctr, Indonesian Med Educ & Res Inst, Jakarta 10430, Indonesia
[4] Univ Muhammadiyah Palembang, Fac Med, Palembang 30263, Indonesia
关键词
Advanced-stage; Cytotoxic T-lymphocyte-associated protein 4; Hodgkin lymphoma; International prognostic score; CTLA-4; IMMUNOTHERAPY; UPDATE;
D O I
10.1186/s13104-024-06853-1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
ObjectiveTwenty percent of all classical Hodgkin lymphoma (CHL) cases relapse and recur, especially in advanced stages with a high International Prognostic Score (IPS). Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a regulatory molecule that can inhibit the immune response and is related to tumor aggressiveness. This study aimed to determine the relationship between CTLA-4 expression in advanced-stage CHL and IPS, identifying it as a potential therapy target. ResultsIn advanced-stage CHL, the group with a high IPS exhibited significantly higher mean CTLA-4 expression compared to the group with a low IPS (p = 0.003).The group with Hb level < 10.5 g/dl, leukocyte count > 15,000/mu L, lymphocyte count < 8%, albumin level < 4 g/dl, and stage 4 exhibited higher CTLA-4 expression than the other group, although only leukocyte count and stage showed statistical significance (p = 0.004 and p = 0.020). Mean CTLA-4 expression was 239.84 +/- 76.36 for nodular sclerosis, 293.95 +/- 147.94 for mixed cellularity, 271.4 +/- 23.56 for lymphocyte depleted, and 225.2 for lymphocyte-rich subtypes. The results suggest that CTLA-4 expression is associated with adverse prognostic factors in the IPS for advanced-stage CHL, supporting the notion that immune checkpoints play a role in cancer progression.
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页数:7
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