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Recombinant human thrombopoietin prior to mobilization chemotherapy facilitates platelet recovery in autologous transplantation in patients with lymphoma: Results of a prospective randomized study

Authors :
Jianliang Yang
Zhishang Zhang
Yan Qin
Le Tang
Sheng Yang
Fengyi Zhao
Shuxiang Zhang
Xiaohui He
Yuankai Shi
Peng Liu
Lin Gui
Weicai Su
Xiaohong Han
Jiarui Yao
Shengyu Zhou
Hongnan Mo
Source :
Chronic Diseases and Translational Medicine, Vol 7, Iss 3, Pp 190-198 (2021), Chronic Diseases and Translational Medicine
Publication Year :
2021
Publisher :
KeAi Communications Co., Ltd., 2021.

Abstract

Background: Chemotherapy plus granulocyte colony-stimulating factor (GCSF) regimen is one of the available approaches to mobilize peripheral blood progenitor cells (PBPCs). It causes thrombocytopenia and delays leukapheresis. This study aimed to evaluate the role of recombinant human thrombopoietin (rhTPO) before mobilization chemotherapy in facilitating leukapheresis in patients with lymphoma. Methods: In this randomized open-label phase 2 trial, patients were randomly assigned in a 1:2 ratio to receive mobilization with rhTPO plus GCSF in combination with chemotherapy (the rhTPO plus GCSF arm) or GCSF alone in combination with chemotherapy (the GCSF alone arm). The recovery of neutrophils and platelets and the amount of platelet transfusion were monitored. Results: Thirty patients were enrolled in this study between March 2016 and August 2018. Patients in the rhTPO plus GCSF arm (n = 10) had similar platelet nadir after mobilization chemotherapy (P=0.878) and similar amount of platelet transfusion (median 0 vs. 1 unit, P=0.735) when compared with the GCSF alone arm (n = 20). On the day of leukapheresis, the median platelet count was 86 × 109/L (range 18–219) among patients who received rhTPO and 73 × 109/L (range 42–197) among those who received GCSF alone (P=0.982). After the use of rhTPO, the incidence of platelet count

Details

Language :
English
Volume :
7
Issue :
3
Database :
OpenAIRE
Journal :
Chronic Diseases and Translational Medicine
Accession number :
edsair.doi.dedup.....33d97e2b2bcdfb00794646d002f38d3a