Safety and performance of theSpectraOptia apheresis system for white blood cell depletion in patients with elevated white blood cell counts

Author:

Lopert Pamela1ORCID,Abdelrahman Sohair1,Graybill Christopher A.1,Rhodes Jack1,Dierickx Daan2,Schäfer Richard3,Reti Marienn4,Wu Depei5,Hu Yu6,Huang Fen7,Hu Jianda8,He Pengcheng9,Liu Ligen10,Li Ming11,Zhang Xuejun12,Bill Jerry1

Affiliation:

1. Terumo BCT, Inc. Lakewood Colorado USA

2. UZ Leuven Leuven Belgium

3. Institute for Transfusion Medicine and Immunohaematology German Red Cross Blood Donor Service Baden‐Württemberg‐Hessen gGmbH Frankfurt Germany

4. Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases Szent Laszla Hospital Campus Budapest Hungary

5. The First Affiliated Hospital of Soochow University Suzhou China

6. Wuhan Union Hospital Wuhan China

7. Nanfang Hospital Guangzhou China

8. Fujian Medical University Union Hospital Fujian China

9. The First Affiliated Hospital of Xi'an Jiaotong University Xi'an China

10. Tongren Hospital Shanghai Jiaotong University School of Medicine Shanghai China

11. The Second People’s Hospital of Shenzhen Shenzhen China

12. The Second Hospital of Hebei Medical University Xi'an China

Abstract

AbstractBackgroundFor the past 30 years, white blood cell depletion (WBCD) or leukocytapheresis has been conducted to rapidly reduce excessive circulating white blood cell (WBC) concentrations in patients at risk for or with symptoms of leukostasis due to hyperleukocytosis. The goal of leukocytapheresis is to prevent or treat acute complications from leukostasis, thereby enabling patients to receive potentially curative chemotherapy.MethodsThis report details the results from a retrospective and a prospective clinical study conducted in the European Union and the People's Republic of China, which assessed the use of the Spectra Optia Apheresis System for leukocytapheresis in patients with hyperleukocytosis. The primary objective of both studies was to the assess the safety and performance of the WBCD procedure in patients with elevated WBC counts.ResultsData were collected from 72 participants completing 87 WBCD procedures. The mean percent change in participant WBC counts post‐procedure was 50.3 ± 21.2% and the collection efficiency (CE1) of the WBCD procedures was 53.7 ± 19.8%. Sixty‐one participants (95.3%) experienced a total of 279 adverse events (AEs) with the majority of the AEs related to post‐procedure changes in laboratory values, which is an anticipated AE in this patient population.ConclusionThe data collected within these studies indicate that the WBCD procedure is safe and well tolerated in patients with hyperleukocytosis as evaluated by percent decrease in WBC count, CE1, and AE incidence.

Funder

Terumo BCT

Publisher

Wiley

Subject

Hematology,General Medicine

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