ايهاب محروس عواض عرابى
أستاذ
Prognostic values of MYD88 and TBLR1expression in tissues of diffuse large B cell non-Hodgkin lymphoma patients; an immunohistochemical study
Contemp Oncol (Pozn) • 2022
معلومات البحث
المؤلفون
Asmaa Hussein Mohamed1, Mariem A. Elfeky1, Shereen Elshorbagy2, Nabila Hefzi3, Tamer Oraby4, Waleed A. Abdelhady5, Mahmoud Sharaf Eldein6 , Ahmed Embaby6, Ehab M. Oraby7
الكلمات المفتاحية
MYD88; TBLR1; immunohistochemistry; diffuse large B cell lymphoma; prognosis
المجلة العلمية
Contemp Oncol (Pozn)
الناشر
Not Available
المجلد
26
العدد
1
الصفحات
49-58
publication.type
International
رابط البحث
Open Link
المواد المرفقة
Not Available
الملخص
Background: Diffuse large B cell non-Hodgkin lymphoma (DLBCL) is the greatest common category of adult lymphoma. Recurrence and treatment resistance happened in one‑third of cases, triggering them to the progressive stage of DL BCL after treatment. Detection of novel predictive and prognostic biomarkers leads to improvement of its treatment and prognosis.
Aim of the study; was to assess the prognostic roles of protein expression of MYD88 and TBLR1 in tissues of diffuse large B cell non-Hodgkin lymphoma patients.
Material and methods: in the current study we included tissues from 100 cases of DLBCL. For immunohistochemistry, tissues were stained with MYD88 and TBLR1. We followed patients for about 3 years then we correlated their expression with clinic-pathological and prognostic parameters.
Results: higher MYD88 and TBLR1 expressions were associated with presence of B symptoms, fever, night sweat, advanced stage, bone marrow involvement and bulky nodal size, presence of extra-nodal extension, unfavorable RFS and unfavorable OS rates (p
Aim of the study; was to assess the prognostic roles of protein expression of MYD88 and TBLR1 in tissues of diffuse large B cell non-Hodgkin lymphoma patients.
Material and methods: in the current study we included tissues from 100 cases of DLBCL. For immunohistochemistry, tissues were stained with MYD88 and TBLR1. We followed patients for about 3 years then we correlated their expression with clinic-pathological and prognostic parameters.
Results: higher MYD88 and TBLR1 expressions were associated with presence of B symptoms, fever, night sweat, advanced stage, bone marrow involvement and bulky nodal size, presence of extra-nodal extension, unfavorable RFS and unfavorable OS rates (p
