-
Je něco špatně v tomto záznamu ?
Performance of the 2016 ACR-EULAR Myositis Response Criteria in adult dermatomyositis/polymyositis therapeutic trials and consensus profiles
D. Saygin, H. Kim, C. Douglas, B. Erman, J. Wilkerson, JA. McGrath, CV. Oddis, IE. Lundberg, AA. Amato, I. García-De La Torre, H. Chinoy, D. Fiorentino, L. Chung, YW. Song, FW. Miller, N. Ruperto, J. Vencovsky, R. Aggarwal, LG. Rider,...
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, N.I.H., Intramural
Grantová podpora
HHSN273201600011C
NIEHS NIH HHS - United States
ZIA AR041215
Intramural NIH HHS - United States
ZIA ES101081
Intramural NIH HHS - United States
NLK
Free Medical Journals
od 1996 do Před 1 rokem
Open Access Digital Library
od 1996-01-01
Medline Complete (EBSCOhost)
od 1999-01-01 do Před 1 rokem
- MeSH
- dermatomyozitida * farmakoterapie MeSH
- dospělí MeSH
- konsensus MeSH
- lidé MeSH
- myozitida * farmakoterapie MeSH
- polymyozitida * farmakoterapie MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Intramural MeSH
OBJECTIVE: The ACR-EULAR Myositis Response Criteria (MRC) were developed as a composite measure using absolute percentage change in six core set measures (CSMs). We aimed to further validate the MRC by assessing the contribution of each CSM, frequency of strength vs extramuscular activity improvement, representation of patient-reported outcome measures (PROM), and frequency of CSM worsening. METHODS: Data from adult dermatomyositis/polymyositis patients in the rituximab (n = 147), etanercept (n = 14), and abatacept (n = 19) trials, and consensus patient profiles (n = 232) were evaluated. The Total Improvement Score (TIS), number of improving vs worsening CSMs, frequency of improvement with and without muscle-related CSMs, and contribution of PROM were evaluated by MRC category. Regression analysis was performed to assess contribution of each CSM to the MRC. RESULTS: Of 412 adults with dermatomyositis/polymyositis, there were 37%, 24%, 25%, and 14% with no, minimal, moderate, and major MRC improvement, respectively. The number of improving CSMs and absolute percentage change in all CSMs increased by improvement category. In minimal-moderate improvement, only physician-reported disease activity contributed significantly more than expected by MRC. Of patients with at least minimal improvement, 95% had improvement in muscle-related measures and a majority (84%) had improvement in PROM. Patients with minimal improvement had worsening in a median of 1 CSM, and most patients with moderate-major improvement had no worsening CSMs. Physician assessment of change generally agreed with MRC improvement categories. CONCLUSION: The ACR-EULAR MRC performs consistently across multiple studies, further supporting its use as an efficacy end point in future myositis therapeutic trials.
Charles University Prague Czech Republic
Department of Dermatology Stanford University School of Medicine Redwood City CA USA
Department of Neurology Brigham and Women's Hospital Harvard Medical School Boston MA USA
Department of Rheumatology 1st Medical Faculty Institute of Rheumatology
IRCCS Istituto Giannina Gaslini UOSID Centro Trial Reumatologia Pediatria 2 PRINTO Genoa Italy
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24000752
- 003
- CZ-PrNML
- 005
- 20240213093345.0
- 007
- ta
- 008
- 240109s2023 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1093/rheumatology/kead110 $2 doi
- 035 __
- $a (PubMed)36929923
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Saygin, Didem $u Section of Rheumatology at University of Chicago and Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA $1 https://orcid.org/000000031675597X
- 245 10
- $a Performance of the 2016 ACR-EULAR Myositis Response Criteria in adult dermatomyositis/polymyositis therapeutic trials and consensus profiles / $c D. Saygin, H. Kim, C. Douglas, B. Erman, J. Wilkerson, JA. McGrath, CV. Oddis, IE. Lundberg, AA. Amato, I. García-De La Torre, H. Chinoy, D. Fiorentino, L. Chung, YW. Song, FW. Miller, N. Ruperto, J. Vencovsky, R. Aggarwal, LG. Rider, International Myositis Assessment and Clinical Studies Group (IMACS)
- 520 9_
- $a OBJECTIVE: The ACR-EULAR Myositis Response Criteria (MRC) were developed as a composite measure using absolute percentage change in six core set measures (CSMs). We aimed to further validate the MRC by assessing the contribution of each CSM, frequency of strength vs extramuscular activity improvement, representation of patient-reported outcome measures (PROM), and frequency of CSM worsening. METHODS: Data from adult dermatomyositis/polymyositis patients in the rituximab (n = 147), etanercept (n = 14), and abatacept (n = 19) trials, and consensus patient profiles (n = 232) were evaluated. The Total Improvement Score (TIS), number of improving vs worsening CSMs, frequency of improvement with and without muscle-related CSMs, and contribution of PROM were evaluated by MRC category. Regression analysis was performed to assess contribution of each CSM to the MRC. RESULTS: Of 412 adults with dermatomyositis/polymyositis, there were 37%, 24%, 25%, and 14% with no, minimal, moderate, and major MRC improvement, respectively. The number of improving CSMs and absolute percentage change in all CSMs increased by improvement category. In minimal-moderate improvement, only physician-reported disease activity contributed significantly more than expected by MRC. Of patients with at least minimal improvement, 95% had improvement in muscle-related measures and a majority (84%) had improvement in PROM. Patients with minimal improvement had worsening in a median of 1 CSM, and most patients with moderate-major improvement had no worsening CSMs. Physician assessment of change generally agreed with MRC improvement categories. CONCLUSION: The ACR-EULAR MRC performs consistently across multiple studies, further supporting its use as an efficacy end point in future myositis therapeutic trials.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a dermatomyozitida $x farmakoterapie $7 D003882
- 650 _2
- $a konsensus $7 D032921
- 650 _2
- $a výsledek terapie $7 D016896
- 650 12
- $a polymyozitida $x farmakoterapie $7 D017285
- 650 12
- $a myozitida $x farmakoterapie $7 D009220
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 655 _2
- $a Research Support, N.I.H., Intramural $7 D052060
- 700 1_
- $a Kim, Hanna $u Juvenile Myositis Pathogenesis and Therapeutics Unit, National Institute of Arthritis Musculoskeletal and Skin Diseases, National Institutes of Health (NIH), Bethesda, MD, USA $1 https://orcid.org/0000000205956533
- 700 1_
- $a Douglas, Christian $u Social & Scientific Systems, Inc, Durham, NC, USA
- 700 1_
- $a Erman, Brian $u Social & Scientific Systems, Inc, Durham, NC, USA
- 700 1_
- $a Wilkerson, Jesse $u Social & Scientific Systems, Inc, Durham, NC, USA
- 700 1_
- $a McGrath, John A $u Social & Scientific Systems, Inc, Durham, NC, USA
- 700 1_
- $a Oddis, Chester V $u Section of Rheumatology at University of Chicago and Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA
- 700 1_
- $a Lundberg, Ingrid E $u Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden $1 https://orcid.org/0000000260689212
- 700 1_
- $a Amato, Anthony A $u Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA
- 700 1_
- $a García-De La Torre, Ignacio $u Hospital General de Occidente de la Secretaría de Salud and Universidad de Guadalajara, Department of Immunology and Rheumatology, Mexico
- 700 1_
- $a Chinoy, Hector $u National Institute for Health Research Manchester Biomedical Research Centre, Division of Musculoskeletal and Dermatological Sciences, Manchester University NHS Foundation Trust, The University of Manchester, Manchester, UK $1 https://orcid.org/0000000164921288
- 700 1_
- $a Fiorentino, David $u Department of Dermatology, Stanford University School of Medicine, Redwood City, CA, USA
- 700 1_
- $a Chung, Lorinda $u Department of Dermatology, Stanford University School of Medicine, Redwood City, CA, USA
- 700 1_
- $a Song, Yeong-Wook $u Medical Research Center, Institute of Human-Environment Interface Biology, Department of Internal Medicine, Seoul National University $1 https://orcid.org/0000000215759007
- 700 1_
- $a Miller, Frederick W $u Environmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA
- 700 1_
- $a Ruperto, Nicolino $u IRCCS Istituto Giannina Gaslini, UOSID Centro Trial, Reumatologia, Pediatria II, PRINTO, Genoa, Italy $1 https://orcid.org/0000000184077782
- 700 1_
- $a Vencovsky, Jiri $u Department of Rheumatology, 1st Medical Faculty, Institute of Rheumatology; Charles University, Prague, Czech Republic
- 700 1_
- $a Aggarwal, Rohit $u Section of Rheumatology at University of Chicago and Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA
- 700 1_
- $a Rider, Lisa G $u Environmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA $1 https://orcid.org/0000000269122458
- 710 2_
- $a International Myositis Assessment and Clinical Studies Group (IMACS)
- 773 0_
- $w MED00011379 $t Rheumatology $x 1462-0332 $g Roč. 62, č. 11 (2023), s. 3672-3679
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/36929923 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20240109 $b ABA008
- 991 __
- $a 20240213093342 $b ABA008
- 999 __
- $a ok $b bmc $g 2049401 $s 1210446
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 62 $c 11 $d 3672-3679 $e 2023Nov02 $i 1462-0332 $m Rheumatology $n Rheumatology (Oxford) $x MED00011379
- GRA __
- $a HHSN273201600011C $p NIEHS NIH HHS $2 United States
- GRA __
- $a ZIA AR041215 $p Intramural NIH HHS $2 United States
- GRA __
- $a ZIA ES101081 $p Intramural NIH HHS $2 United States
- LZP __
- $a Pubmed-20240109