PMID- 35547942 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220716 IS - 2168-8184 (Print) IS - 2168-8184 (Electronic) IS - 2168-8184 (Linking) VI - 14 IP - 5 DP - 2022 May TI - Serum Tumor Necrosis Factor-Alpha Levels in Acute Leukemia and Its Prognostic Significance. PG - e24835 LID - 10.7759/cureus.24835 [doi] LID - e24835 AB - Introduction Tumor necrosis factor-alpha (TNF-alpha) is a pleiotropic cytokine that facilitates malignant cells in immune evasion, survival, and treatment resistance by generating a favorable milieu for them. It is shown to be ectopically produced by malignant/leukemic and immune cells in the tumor microenvironment, providing a tumor-supportive environment and playing an important part in the establishment and progression of malignant cells. It is linked to hyperleukocytosis, high blast count, and poor clinical outcomes in acute leukemia (AL). Considering the varied role and different expression patterns of tumor necrosis factor-alpha in acute leukemia and its clinical relevance, the present study was planned to monitor the level of tumor necrosis factor-alpha in patients with acute leukemia and its correlation with disease outcome. The aim of this study was to monitor the level of tumor necrosis factor-alpha in patients with acute leukemia at the time of diagnosis and after induction chemotherapy. Material and methods The study included cases classified as acute leukemia based on morphological examination, bone marrow analysis, and flow cytometry. In all patients with acute leukemia (n = 90) and controls (n = 10), the serum tumor necrosis factor-alpha level was measured using a Diaclone Human ELISA kit (Diaclone, Besancon, France) (solid phase sandwich ELISA) at diagnosis and after induction chemotherapy. Results Tumor necrosis factor-alpha levels were substantially higher in T-acute lymphoblastic leukemia (T-ALL) cases, followed by acute myeloid leukemia (AML) and B-acute lymphoblastic leukemia (B-ALL), at the time of diagnosis, compared to the control. A significant reduction in serum tumor necrosis factor-alpha level was seen in patients with acute leukemia after induction phase chemotherapy (P < 0.05). Tumor necrosis factor-alpha levels were considerably reduced (P < 0.001) in the majority of acute leukemia cases after the induction phase, while high tumor necrosis factor-alpha levels were positively correlated with incomplete remission status in the remaining cases. Conclusion Tumor necrosis factor-alpha is involved in the progression of acute leukemia and its relapse. High levels of tumor necrosis factor-alpha are linked to leukocytosis, high blast counts, and worse survival in patients with acute leukemia. Monitoring of tumor necrosis factor-alpha may be helpful in patients with acute leukemia in view of available antitumor necrosis factor-alpha therapy. CI - Copyright (c) 2022, Verma et al. FAU - Verma, Sapana AU - Verma S AD - Department of Pathology, King George's Medical University, Lucknow, IND. FAU - Singh, Anurag AU - Singh A AD - Department of Pathology, King George's Medical University, Lucknow, IND. FAU - Yadav, Geeta AU - Yadav G AD - Department of Pathology, King George's Medical University, Lucknow, IND. FAU - Kushwaha, Rashmi AU - Kushwaha R AD - Department of Pathology, King George's Medical University, Lucknow, IND. FAU - Ali, Wahid AU - Ali W AD - Department of Pathology, King George's Medical University, Lucknow, IND. FAU - Verma, Shailendra P AU - Verma SP AD - Department of Hematology and Oncology/Clinical Hematology, King George's Medical University, Lucknow, IND. FAU - Singh, U S AU - Singh US AD - Department of Pathology, King George's Medical University, Lucknow, IND. LA - eng PT - Journal Article DEP - 20220508 PL - United States TA - Cureus JT - Cureus JID - 101596737 PMC - PMC9090230 OTO - NOTNLM OT - bone marrow examination OT - elisa OT - flow cytometry OT - leukemia OT - tumor necrosis factor-alpha COIS- The authors have declared that no competing interests exist. EDAT- 2022/05/14 06:00 MHDA- 2022/05/14 06:01 PMCR- 2022/05/08 CRDT- 2022/05/13 11:20 PHST- 2022/05/08 00:00 [accepted] PHST- 2022/05/13 11:20 [entrez] PHST- 2022/05/14 06:00 [pubmed] PHST- 2022/05/14 06:01 [medline] PHST- 2022/05/08 00:00 [pmc-release] AID - 10.7759/cureus.24835 [doi] PST - epublish SO - Cureus. 2022 May 8;14(5):e24835. doi: 10.7759/cureus.24835. eCollection 2022 May.