Predictive factors of poor blood collecting flow during leukocyte apheresis for cellular therapy
Saori Konno
Department of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan
Division of Blood Transfusion, Shinshu University Hospital, Matsumoto, Japan
Search for more papers by this authorCorresponding Author
Ryu Yanagisawa
Division of Blood Transfusion, Shinshu University Hospital, Matsumoto, Japan
Center for Advanced Cell Therapy, Shinshu University Hospital, Matsumoto, Japan
Correspondence
Ryu Yanagisawa, MD, PhD, Division of Blood Transfusion, Shinshu University Hospital, 3-1-1, Asahi, Matsumoto 390-8621, Japan.
Email: [email protected]
Search for more papers by this authorNoriko Motoki
Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this authorShigetaka Shimodaira
Department of Regenerative Medicine, Kanazawa Medical University, Uchinada, Japan
Search for more papers by this authorSaori Konno
Department of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan
Division of Blood Transfusion, Shinshu University Hospital, Matsumoto, Japan
Search for more papers by this authorCorresponding Author
Ryu Yanagisawa
Division of Blood Transfusion, Shinshu University Hospital, Matsumoto, Japan
Center for Advanced Cell Therapy, Shinshu University Hospital, Matsumoto, Japan
Correspondence
Ryu Yanagisawa, MD, PhD, Division of Blood Transfusion, Shinshu University Hospital, 3-1-1, Asahi, Matsumoto 390-8621, Japan.
Email: [email protected]
Search for more papers by this authorNoriko Motoki
Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this authorShigetaka Shimodaira
Department of Regenerative Medicine, Kanazawa Medical University, Uchinada, Japan
Search for more papers by this authorAbstract
Leukocyte apheresis is necessary in various cellular therapies. However, maintenance of a stable flow rate during leukocyte apheresis is often difficult, even in patients or donors without major problems. Despite this, predictive methods and evidence regarding the reality of the situation are limited. We conducted a retrospective analysis involving adult patients who required leukocyte apheresis for the treatment of neoplasms using WT1-pulsed dendritic cell vaccine. Monocytes were separated from apheresis products to obtain dendritic cells. All the patients were pre-evaluated based on laboratory and chest X-ray findings and subjected to an identical apheresis procedure. The occurrence of poor blood collecting flow during leukocyte apheresis was monitored, and the frequency, clinical information, and associated risk factors were analyzed. Among 160 cases, poor blood collecting flow was observed in 53 cases (33.1%) in a median time of 54 min (range, 2–127 min) post-initiation of leukocyte apheresis. Owing to difficulty in obtaining higher collecting flow, a longer procedure time was required, and in some cases, the scheduled apheresis cycles could not be completed. Consequently, the number of harvested monocytes was low. Multivariable analysis indicated that female patients have an increased risk of poor inlet flow rate. Furthermore, prolonged QT dispersion (QTD) calculated using Bazett's formula was found to be a risk factor. Although the patients did not present any major problems during leukocyte apheresis, poor blood collecting flow was observed in some cases. Sex and pre-evaluated QTD might be useful predictors for these cases; however, further prospective evaluation is necessary.
CONFLICT OF INTEREST
The authors have no conflicts of interest to declare.
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