Abstract 350P
Background
Carcinoembryonic antigen (CEACAM) or CD66+ is categorized as type N2 tumour associated neutrophils (TAN), an immunoreceptor expressed on activated neutrophils. It is also known as marker for neutrophil specific granules. This marker is expressed on tumour tissue, has strong immunosuppressive and tumour promoting acttivities including angiogenesis, invasion, and metastasis through various mechanism. This study aimed to assess intratumoural CD66B+ TAN to predict clinical treatment response in patients with diffuse large B cell lymphoma (DLBCL).
Methods
This prognostic study was conducted in Palembang, South Sumatera, Indonesia in 2020. The subjects were 18 - 70 years old DLBCL patients, enrolled by consecutive sampling using medical record. The immunohistochemistry TAN CD66b+ was examined by pathologist. Chemotherapy response was assessed clinically (hematological and radiological) after minimum two cycles of RCHOP regimen. Patients with HIV, relapsed DLBCL, other malignancies, and delayed chemotherapy were excluded.
Results
Of the 21 subjects consisted of 11 men (52,4%), the most subtype (95,2%) was DLBCL non-GCB, prognostic high-risk IPI score 42,9% and intermediate-risk 57,1%. Subjects who achieved complete remission response were 9 people (42,9%). The cut-off value for the CD66b+ TAN density was 21,7 cells/mm2. A total of 76,9% of subjects with high density CD66b+ TAN did not achieve any remission (p=0.029), with sensitivity 83,3% and specificity 66,7%.
Conclusions
We found that density levels of intratumoural CD66b+ TAN in tumour tissue has significant correlation with non-responder (poor prognosis) DLBCL patients.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
217P - Conditional reprogramming of urine-derived bladder cancer cells: A model for precision medicine
Presenter: Yu Dong
Session: Poster Display
Resources:
Abstract
218P - Clinical effectiveness of tislelizumab combined with gemcitabine/cisplatin (GC) versus GC as adjuvant therapy in high-risk muscle-invasive urothelial carcinoma (MIUC): A real-world study
Presenter: xingliang Tan
Session: Poster Display
Resources:
Abstract
219P - Clinical effectiveness of tislelizumab plus TKI as first-line therapy in patients with metastatic renal cell carcinoma (mRCC): A real-world study
Presenter: Pei Dong
Session: Poster Display
Resources:
Abstract
220P - Heterogeneity in tertiary lymphoid structures predicts distinct prognosis and immune microenvironment characterizations of clear cell renal cell carcinoma
Presenter: Wenhao Xu
Session: Poster Display
Resources:
Abstract
221P - Genetic polymorphism of genes encoding cytokines interleukin1 1-alpha and TNF-alpha in non-muscle invasive bladder cancer
Presenter: Anil Kumar
Session: Poster Display
Resources:
Abstract
222P - The association between response to enfortumab vedotin and peripheral neuropathy: A multicenter retrospective study in Japan
Presenter: Nozomi Hayakawa
Session: Poster Display
Resources:
Abstract
223P - Patient and healthcare practitioner preferences for treatments in advanced renal cell carcinoma
Presenter: Niara Oliveira
Session: Poster Display
Resources:
Abstract
224P - WUTSUP-01: Phase II trial of neoadjuvant toripalimab and chemotherapy in locally advanced upper tract urothelial carcinoma
Presenter: Yige Bao
Session: Poster Display
Resources:
Abstract
225P - A novel multianalyte signature for stratifying Indian non-muscle invasive bladder cancer: A single center observational study
Presenter: Hari P S
Session: Poster Display
Resources:
Abstract
226P - Prognosis stratification of immunotherapy by a mutational signature in urothelial carcinoma
Presenter: Xuebing Han
Session: Poster Display
Resources:
Abstract