Cargando…

Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance

AIM: Lusutrombopag is approved for the treatment of thrombocytopenia in chronic liver disease patients undergoing invasive procedures. This real‐world surveillance assesses the safety and effectiveness of lusutrombopag in Japan. METHODS: This ongoing, multicenter, prospective, real‐world surveillanc...

Descripción completa

Detalles Bibliográficos
Autores principales: Sasaki, Ritsue, Shiino, Chikako, Imawari, Michio, Bentley, Roy, Cai, Bin, Yoshida, Manami, Afdhal, Nezam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899664/
https://www.ncbi.nlm.nih.gov/pubmed/31228221
http://dx.doi.org/10.1111/hepr.13392
_version_ 1783477180605399040
author Sasaki, Ritsue
Shiino, Chikako
Imawari, Michio
Bentley, Roy
Cai, Bin
Yoshida, Manami
Afdhal, Nezam
author_facet Sasaki, Ritsue
Shiino, Chikako
Imawari, Michio
Bentley, Roy
Cai, Bin
Yoshida, Manami
Afdhal, Nezam
author_sort Sasaki, Ritsue
collection PubMed
description AIM: Lusutrombopag is approved for the treatment of thrombocytopenia in chronic liver disease patients undergoing invasive procedures. This real‐world surveillance assesses the safety and effectiveness of lusutrombopag in Japan. METHODS: This ongoing, multicenter, prospective, real‐world surveillance is collecting data from case report forms between October 2016 and May 2021. Interim data up to September 2018 were used to evaluate safety (adverse events and adverse drug reactions [ADRs]) and effectiveness (proportion of patients avoiding preoperative platelet transfusion and change in platelet count from baseline). RESULTS: The safety analysis set included 331 patients. The mean baseline platelet count was 46.2 ± 13.7 × 10(9)/L. Of 377 invasive procedures, radiofrequency ablation (110 procedures, 29.2%) was the most frequent. The mean time from starting lusutrombopag treatment to invasive procedure was 12.3 days. Incidences of serious adverse events and ADRs were 8.76% and 3.32%, respectively. Six cases (1.81%) of portal vein thrombosis were considered serious adverse events; of these, four cases (1.21%) were classified as serious ADRs. Of 300 patients who underwent an invasive procedure (excluding those with platelet transfusion refractoriness), 282 (94.0%) avoided preoperative platelet transfusion. In patients with platelet measurements before and after lusutrombopag administration who did not undergo platelet transfusion, the mean maximum change in platelet count from baseline was 41.7 ± 31.4 × 10(9)/L (range, −6 to 276; n = 286). All patients receiving second (n = 20) and third (n = 1) treatments avoided preoperative platelet transfusion without developing any ADRs. CONCLUSIONS: This real‐world surveillance further supports the safety and effectiveness of lusutrombopag in patients with chronic liver disease undergoing invasive procedures.
format Online
Article
Text
id pubmed-6899664
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-68996642019-12-19 Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance Sasaki, Ritsue Shiino, Chikako Imawari, Michio Bentley, Roy Cai, Bin Yoshida, Manami Afdhal, Nezam Hepatol Res Original Articles AIM: Lusutrombopag is approved for the treatment of thrombocytopenia in chronic liver disease patients undergoing invasive procedures. This real‐world surveillance assesses the safety and effectiveness of lusutrombopag in Japan. METHODS: This ongoing, multicenter, prospective, real‐world surveillance is collecting data from case report forms between October 2016 and May 2021. Interim data up to September 2018 were used to evaluate safety (adverse events and adverse drug reactions [ADRs]) and effectiveness (proportion of patients avoiding preoperative platelet transfusion and change in platelet count from baseline). RESULTS: The safety analysis set included 331 patients. The mean baseline platelet count was 46.2 ± 13.7 × 10(9)/L. Of 377 invasive procedures, radiofrequency ablation (110 procedures, 29.2%) was the most frequent. The mean time from starting lusutrombopag treatment to invasive procedure was 12.3 days. Incidences of serious adverse events and ADRs were 8.76% and 3.32%, respectively. Six cases (1.81%) of portal vein thrombosis were considered serious adverse events; of these, four cases (1.21%) were classified as serious ADRs. Of 300 patients who underwent an invasive procedure (excluding those with platelet transfusion refractoriness), 282 (94.0%) avoided preoperative platelet transfusion. In patients with platelet measurements before and after lusutrombopag administration who did not undergo platelet transfusion, the mean maximum change in platelet count from baseline was 41.7 ± 31.4 × 10(9)/L (range, −6 to 276; n = 286). All patients receiving second (n = 20) and third (n = 1) treatments avoided preoperative platelet transfusion without developing any ADRs. CONCLUSIONS: This real‐world surveillance further supports the safety and effectiveness of lusutrombopag in patients with chronic liver disease undergoing invasive procedures. John Wiley and Sons Inc. 2019-07-22 2019-10 /pmc/articles/PMC6899664/ /pubmed/31228221 http://dx.doi.org/10.1111/hepr.13392 Text en © 2019 The Authors. Hepatology Research published by John Wiley & Sons Australia, Ltd on behalf of Japan Society of Hepatology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Sasaki, Ritsue
Shiino, Chikako
Imawari, Michio
Bentley, Roy
Cai, Bin
Yoshida, Manami
Afdhal, Nezam
Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance
title Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance
title_full Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance
title_fullStr Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance
title_full_unstemmed Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance
title_short Safety and effectiveness of lusutrombopag in Japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: Interim results of a postmarketing surveillance
title_sort safety and effectiveness of lusutrombopag in japanese chronic liver disease patients with thrombocytopenia undergoing invasive procedures: interim results of a postmarketing surveillance
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899664/
https://www.ncbi.nlm.nih.gov/pubmed/31228221
http://dx.doi.org/10.1111/hepr.13392
work_keys_str_mv AT sasakiritsue safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance
AT shiinochikako safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance
AT imawarimichio safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance
AT bentleyroy safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance
AT caibin safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance
AT yoshidamanami safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance
AT afdhalnezam safetyandeffectivenessoflusutrombopaginjapanesechronicliverdiseasepatientswiththrombocytopeniaundergoinginvasiveproceduresinterimresultsofapostmarketingsurveillance