Mean Platelet Volume Has Prognostic Value in Chronic Lymphocytic Leukemia.

MPV TTFT chronic lymphocytic leukemia

Journal

Cancer management and research
ISSN: 1179-1322
Titre abrégé: Cancer Manag Res
Pays: New Zealand
ID NLM: 101512700

Informations de publication

Date de publication:
2020
Historique:
received: 17 01 2020
accepted: 08 09 2020
entrez: 29 10 2020
pubmed: 30 10 2020
medline: 30 10 2020
Statut: epublish

Résumé

Mean platelet volume (MPV) is a readily accessible and commonly tested hematological indicator. Recent studies revealed a significant impact of MPV on the course and prognosis of many diseases, including some types of cancer, as well as on the incidence of atrial fibrillation and bleeding. The study aimed to perform a retrospective analysis of MPV in terms of time to first treatment (TTFT) and to determine its prognostic value in the group of patients with chronic lymphocytic leukemia (CLL). Moreover, the study includes a retrospective analysis of platelet parameters in patients treated with ibrutinib concerning bleeding and atrial fibrillation. The study included 523 patients with CLL, for 344 the most important cytogenetic aberrations were reported. The Mann-Whitney, Kruskal-Wallis, Kaplan-Meier, chi-squared, log‑rank tests and multivariate Cox proportional hazard regression model were used to analyze collected data. The receiver operating characteristic curve analysis was performed to identify optimal cut-off value for MPV. The analysis of survival curves showed that in the group of patients with higher values of MPV TTFT was significantly longer than in the group with lower MPV (17.9 vs 36 months, p=0.0015, cut-off value for MPV= 10.4 fl). In multivariate Cox proportional hazard regression model low MPV, the presence of del11q and del13q provided independent prognostic value for TTFT (HR=0.69, 95%-CI, 0.5293 to 0.9081; p=0.0078; HR=1.76, 95%-CI, 1.3000 to 2.3882, p=0.0003, HR=0.74, 95%-Cl, 0.5674 to 0.9588, p=0.0229, respectively). In the group treated with ibrutinib, 59 patients had no significant correlation between MPV level and the incidence of therapy complications, although in the group of patients with low MPV there was a tendency for more frequent occurrence of atrial fibrillation (p=0.259). Low MPV values are associated with unfavorable prognosis and might represent a novel, independent prognostic factor in CLL.

Identifiants

pubmed: 33116854
doi: 10.2147/CMAR.S246385
pii: 246385
pmc: PMC7567945
doi:

Types de publication

Journal Article

Langues

eng

Pagination

9977-9985

Informations de copyright

© 2020 Masternak et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

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Auteurs

Marta Masternak (M)

Department of Experimental Hematooncology, Medical University of Lublin, Lublin, Poland.

Bartosz Puła (B)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Joanna Knap (J)

Department of Experimental Hematooncology, Medical University of Lublin, Lublin, Poland.

Anna Waszczuk-Gajda (A)

Department of Hematology, Oncology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.

Joanna Drozd-Sokołowska (J)

Department of Hematology, Oncology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.

Kamil Wdowiak (K)

Department of Internal Medicine and Oncological Chemotherapy, Silesian Medical University, Katowice, Poland.

Sebastian Grosicki (S)

Department of Hematology and Cancer Prevention in Chorzow, Faculty of Health Sciences in Bytom, Silesian Medical University, Katowice, Poland.

Izabela Kozłowska (I)

Department of Hematology and Cancer Prevention, Municipal Hospital in Chorzów, Chorzów, Poland.

Marta Kaźmierczak (M)

Department of Hematology and Cancer Prevention, Municipal Hospital in Chorzów, Chorzów, Poland.

Anna Łabędź (A)

Department of Hematology, Rydrygier's Hospital in Cracow, Cracow, Poland.

Łukasz Szukalski (Ł)

Department of Hematology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Toruń, Poland.

Kamil Wiśniewski (K)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Edyta Subocz (E)

Department of Hematology, Military Institute of Medicine, Warsaw, Poland; Clinical Department of Hematology, Independent Public Healthcare Centre of the Ministry of Internal Affairs and Administration with Warmia-Mazury Region's Oncology Centre in Olsztyn, Olsztyn, Poland.

Janusz Hałka (J)

Clinical Department of Hematology, Independent Public Healthcare Centre of the Ministry of Internal Affairs and Administration with Warmia-Mazury Region's Oncology Centre in Olsztyn, Olsztyn, Poland.

Agnieszka Szymczyk (A)

Department of Hematooncology and Bone Marrow Transplantation, Medical University of Lublin, Lublin, Poland; Hematology Department, St John's Cancer Center, Lublin, Poland.

Marek Hus (M)

Department of Hematooncology and Bone Marrow Transplantation, Medical University of Lublin, Lublin, Poland.

Krzysztof Jamroziak (K)

Department of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Krzysztof Giannopoulos (K)

Department of Experimental Hematooncology, Medical University of Lublin, Lublin, Poland; Hematology Department, St John's Cancer Center, Lublin, Poland.

Classifications MeSH