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      Chemotherapy-induced thrombocytopenia and platelet transfusion in patients with diffuse large B-cell lymphoma

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          Abstract

          Background

          Currently, the risk factors associated with chemotherapy-induced thrombocytopenia (CIT) in patients with diffuse large B-cell lymphoma (DLBCL) are still undefined. Our study aimed to analyze the effects of risk factors on thrombocytopenia and to identify the threshold for infusion platelets of CIT patients who have received platelet transfusions.

          Methods

          We conducted a retrospective analysis of 523 patients with DLBCL from 2011 to 2013. The clinical and demographic parameters were extracted, and the risk factors associated with CIT were analyzed. The threshold for platelet transfusions in DLBCL patients with a central venous catheter (CVC) was evaluated.

          Results

          A total of 227 (43.4%) DLBCL patients had thrombocytopenia, and 63 (12.0%) had thrombocytopenia without concomitant cytopenia. We found that the choice of chemotherapy regimen was positively correlated with thrombocytopenia (P<0.001). The chemotherapy regimens most likely to result in thrombocytopenia were dexamethasone, cytarabine, cisplatin (DHAP) (92.3%), isophosphamide, carboplatin, etoposide (ICE) (89.7%), gemcitabine, dexamethasone, cisplatin (GDP) (89.7%), gemcitabine, and oxaliplatin (Gemox) (69.0%). In addition to these, high lactate dehydrogenase (LDH) (P=0.004) and Ann Arbor stage III/IV (P=0.024) were determined to be risk factors leading to thrombocytopenia. Forty patients (17.6%) had transfused platelets, and all of them were placed in the CVC. The high-threshold group (platelet count ≤20×10 9/L had a significantly lower amount of platelet transfusions than the low-threshold group ≤10×10 9/L. The platelet transfusion amount was 1.44±0.77 vs. 2.05±1.13 (P=0.047), respectively.

          Conclusions

          The chemotherapy regimens of DHAP, ICE, GDP, and Gemox can easily lead to thrombocytopenia. A high level of LDH in the peripheral blood and Ann Arbor stage III/IV are also associated with risk factors for thrombocytopenia. A 20×10 9/L prophylactic platelet transfusion threshold value is safer, more effective, and thus a better choice for DLBCL patients with CVC.

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          Most cited references46

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          The 2008 WHO classification of lymphoid neoplasms and beyond: evolving concepts and practical applications.

          The World Health Organization classification of lymphoid neoplasms updated in 2008 represents a worldwide consensus on the diagnosis of these tumors and is based on the recognition of distinct diseases, using a multidisciplinary approach. The updated classification refined the definitions of well-recognized diseases, identified new entities and variants, and incorporated emerging concepts in the understanding of lymphoid neoplasms. However, some questions were unresolved, such as the extent to which specific genetic or molecular alterations define certain tumors, and the status of provisional entities, categories for which the World Health Organization working groups felt there was insufficient evidence to recognize as distinct diseases at this time. In addition, since its publication, new findings and ideas have been generated. This review summarizes the scientific rationale for the classification, emphasizing changes that have had an effect on practice guidelines. The authors address the criteria and significance of early or precursor lesions and the identification of certain lymphoid neoplasms largely associated with particular age groups, such as children and the elderly. The issue of borderline categories having overlapping features with large B-cell lymphomas, as well as several provisional entities, is reviewed. These new observations chart a course for future research in the field.
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            Platelet transfusion: a clinical practice guideline from the AABB.

            The AABB (formerly, the American Association of Blood Banks) developed this guideline on appropriate use of platelet transfusion in adult patients.
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              Lactate dehydrogenase 5: an old friend and a new hope in the war on cancer.

              A hallmark of most cancer cells is an altered metabolism involving a shift to aerobic glycolysis with lactate production coupled with a higher uptake of glucose as the main source of energy. Lactate dehydrogenase 5 (LDH-5) catalyzes the reduction of pyruvate by NADH to form lactate, thus determining the availability of NAD(+) to maintain the continuity of glycolysis. It is therefore an important control point in the system of cellular energy release. Its upregulation is common in many malignant tumors. Inhibiting LDH-5 activity has an anti-proliferative effect on cancer cells. It may reverse their resistance to conventional chemo- and radiotherapy. Recent research has renewed interest in LDH-5 as an anticancer drug target. This review summarizes recent studies exploring the role of LDH-5 in cancer growth, its utility as a tumor marker, and developments made in identifying and designing anti-LDH-5 therapeutic agents.
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                Author and article information

                Journal
                Transl Cancer Res
                Transl Cancer Res
                TCR
                Translational Cancer Research
                AME Publishing Company
                2218-676X
                2219-6803
                March 2020
                March 2020
                : 9
                : 3
                : 1640-1651
                Affiliations
                [1 ]Department of Blood Transfusion, Fujian Cancer Hospital, Fujian Medical University Cancer Hospital, Fuzhou350014 , China;
                [2 ]Fujian Provincial Key Laboratory of Tumor Biotherapy, Fuzhou350014 , China
                Author notes

                Contributions: (I) Conception and design: R Lu, X Ye; (II) Administrative support: None; (III) Provision of study materials or patients: None; (IV) Collection and assembly of data: R Lu, Q Lin, S Chen; (V) Data analysis and interpretation: R Lu; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

                Correspondence to: Xianren Ye, PhD. Department of Blood Transfusion, Fujian Cancer Hospital, Fujian Medical University Cancer Hospital, 420 Fuma Road, Jin’an District, Fuzhou 350014, China. Email: fjthy@ 123456sina.com .
                Article
                tcr-09-03-1640
                10.21037/tcr.2020.01.64
                8798421
                35117512
                46e393ce-0d31-451e-90cd-998d533a143b
                2020 Translational Cancer Research. All rights reserved.

                Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

                History
                : 31 August 2019
                : 06 January 2020
                Funding
                Funded by: the Fujian Provincial Health Technology Project
                Award ID: grant number: 2016-ZQN-19
                Funded by: the Science and Technology Program of Fujian Province, China
                Award ID: grant number: 2018Y2003
                Funded by: the National Clinical Key Specialty Construction Program of China
                Categories
                Original Article

                diffuse large b-cell lymphoma,platelet transfusion,chemotherapy regimen,chemotherapy-induced thrombocytopenia,central venous catheterization

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