-
Je něco špatně v tomto záznamu ?
Effectiveness and Safety of Romiplostim Among Patients with Newly Diagnosed, Persistent and Chronic Immune Thrombocytopenia in European Clinical Practice
SJ. Snell Taylor, CM. Nielson, A. Breskin, B. Saul, Y. Yu, N. Alam, M. Eisen, J. Hippenmeyer, A. Janssens, T. Kozak, HA. Papadaki, D. Selleslag, JF. Viallard, C. Feistritzer, G. Kaiafa, M. Kelsh, K. Kilpatrick, MA. Brookhart, LJ. McGrath
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- dospělí MeSH
- idiopatická trombocytopenická purpura * diagnóza farmakoterapie MeSH
- lidé MeSH
- receptory Fc terapeutické užití MeSH
- rekombinantní fúzní proteiny MeSH
- thrombopoetin škodlivé účinky MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Evropa MeSH
INTRODUCTION: Romiplostim has been approved in Europe since 2009 to treat patients with chronic primary immune thrombocytopenia (ITP). Using real-world data from seven European countries, we measured the effectiveness and safety outcomes within 24 weeks following romiplostim initiation by duration of ITP: less than 3 months ("newly diagnosed"), 3-12 months ("persistent"), and more than 12 months ("chronic"). METHODS: Adults with ITP and ≥ 1 romiplostim administration between 2009 and 2012 were included. Endpoints included durable platelet response, median platelet count, rescue therapy, bleeding and adverse events. We used inverse probability of censoring weighted estimators to estimate cumulative risk of each outcome. There were 64 newly diagnosed, 50 persistent, and 226 chronic ITP patients at romiplostim initiation. RESULTS: Durable platelet response at 24 weeks ranged from 32% [confidence interval (CI): 18-46%] in newly diagnosed patients to 53% (CI 37-68%) in persistent patients. Median platelet count during follow-up ranged from 88 (CI 80-96) × 109/L in chronic patients to 131 (CI 102-160) × 109/L in newly diagnosed patients. CONCLUSION: Regardless of ITP duration, over half of patients discontinued concomitant ITP medications. Few adverse events were observed. Although only approved for chronic patients, estimates of the romiplostim treatment effect were similar across patients being managed in European clinical practice, regardless of ITP duration at romiplostim initiation.
AHEPA University Hospital Aristotle University of Thessaloniki Thessaloniki Greece
Algemeen Ziekenhuis Sint Jan Bruge Belgium
Amgen Inc Rotkreuz Switzerland
Charles University Prague Czech Republic
Department of Epidemiology University of North Carolina at Chapel Hill Chapel Hill USA
Department of Population Health Sciences Duke University Durham UK
Hospital du Haut Leveque Pessac France
NoviSci Inc 201 W Main St Ste 101 Durham NC 27701 USA
Universitätsklinik für Innere Medizin 5 Innsbruck Innsbruck Austria
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21018648
- 003
- CZ-PrNML
- 005
- 20210830100239.0
- 007
- ta
- 008
- 210728s2021 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12325-021-01727-5 $2 doi
- 035 __
- $a (PubMed)33866516
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Snell Taylor, Sara J $u NoviSci, Inc., 201 W Main St, Ste 101, Durham, NC, 27701, USA. staylor@novisci.com
- 245 10
- $a Effectiveness and Safety of Romiplostim Among Patients with Newly Diagnosed, Persistent and Chronic Immune Thrombocytopenia in European Clinical Practice / $c SJ. Snell Taylor, CM. Nielson, A. Breskin, B. Saul, Y. Yu, N. Alam, M. Eisen, J. Hippenmeyer, A. Janssens, T. Kozak, HA. Papadaki, D. Selleslag, JF. Viallard, C. Feistritzer, G. Kaiafa, M. Kelsh, K. Kilpatrick, MA. Brookhart, LJ. McGrath
- 520 9_
- $a INTRODUCTION: Romiplostim has been approved in Europe since 2009 to treat patients with chronic primary immune thrombocytopenia (ITP). Using real-world data from seven European countries, we measured the effectiveness and safety outcomes within 24 weeks following romiplostim initiation by duration of ITP: less than 3 months ("newly diagnosed"), 3-12 months ("persistent"), and more than 12 months ("chronic"). METHODS: Adults with ITP and ≥ 1 romiplostim administration between 2009 and 2012 were included. Endpoints included durable platelet response, median platelet count, rescue therapy, bleeding and adverse events. We used inverse probability of censoring weighted estimators to estimate cumulative risk of each outcome. There were 64 newly diagnosed, 50 persistent, and 226 chronic ITP patients at romiplostim initiation. RESULTS: Durable platelet response at 24 weeks ranged from 32% [confidence interval (CI): 18-46%] in newly diagnosed patients to 53% (CI 37-68%) in persistent patients. Median platelet count during follow-up ranged from 88 (CI 80-96) × 109/L in chronic patients to 131 (CI 102-160) × 109/L in newly diagnosed patients. CONCLUSION: Regardless of ITP duration, over half of patients discontinued concomitant ITP medications. Few adverse events were observed. Although only approved for chronic patients, estimates of the romiplostim treatment effect were similar across patients being managed in European clinical practice, regardless of ITP duration at romiplostim initiation.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a idiopatická trombocytopenická purpura $x diagnóza $x farmakoterapie $7 D016553
- 650 _2
- $a receptory Fc $x terapeutické užití $7 D011961
- 650 _2
- $a rekombinantní fúzní proteiny $7 D011993
- 650 _2
- $a thrombopoetin $x škodlivé účinky $7 D013926
- 651 _2
- $a Evropa $7 D005060
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Nielson, Carrie M $u Amgen Inc., Thousand Oaks, USA
- 700 1_
- $a Breskin, Alexander $u NoviSci, Inc., 201 W Main St, Ste 101, Durham, NC, 27701, USA $u Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, USA
- 700 1_
- $a Saul, Bradley $u NoviSci, Inc., 201 W Main St, Ste 101, Durham, NC, 27701, USA
- 700 1_
- $a Yu, Ying $u NoviSci, Inc., 201 W Main St, Ste 101, Durham, NC, 27701, USA
- 700 1_
- $a Alam, Naufil $u Amgen Ltd, Uxbridge, UK
- 700 1_
- $a Eisen, Melissa $u Amgen Inc., Thousand Oaks, USA
- 700 1_
- $a Hippenmeyer, Jane $u Amgen Inc., Rotkreuz, Switzerland
- 700 1_
- $a Janssens, Ann $u University Hospitals Leuven, Leuven, Belgium
- 700 1_
- $a Kozak, Tomas $u Charles University, Prague, Czech Republic
- 700 1_
- $a Papadaki, Helen A $u University Hospital of Heraklion, Heraklion, Greece
- 700 1_
- $a Selleslag, Dominik $u Algemeen Ziekenhuis Sint-Jan, Bruge, Belgium
- 700 1_
- $a Viallard, Jean-Francois $u Hospital du Haut Leveque, Pessac, France
- 700 1_
- $a Feistritzer, Clemens $u Universitätsklinik für Innere Medizin V Innsbruck, Innsbruck, Austria
- 700 1_
- $a Kaiafa, Georgia $u AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece
- 700 1_
- $a Kelsh, Michael $u Amgen Inc., Thousand Oaks, USA
- 700 1_
- $a Kilpatrick, Karynsa $u Amgen Inc., Thousand Oaks, USA
- 700 1_
- $a Brookhart, M Alan $u NoviSci, Inc., 201 W Main St, Ste 101, Durham, NC, 27701, USA $u Department of Population Health Sciences, Duke University, Durham, UK
- 700 1_
- $a McGrath, Leah J $u NoviSci, Inc., 201 W Main St, Ste 101, Durham, NC, 27701, USA
- 773 0_
- $w MED00179771 $t Advances in therapy $x 1865-8652 $g Roč. 38, č. 5 (2021), s. 2673-2688
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33866516 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20210830100239 $b ABA008
- 999 __
- $a ok $b bmc $g 1689674 $s 1139094
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 38 $c 5 $d 2673-2688 $e 20210418 $i 1865-8652 $m Advances in therapy $n Adv Ther $x MED00179771
- LZP __
- $a Pubmed-20210728