<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Burmester GR</dc:creator>
  <dc:creator>Kaeley GS</dc:creator>
  <dc:creator>Kavanaugh AF</dc:creator>
  <dc:creator>Gabay C</dc:creator>
  <dc:creator>MacCarter DK</dc:creator>
  <dc:creator>Nash P</dc:creator>
  <dc:creator>Takeuchi T</dc:creator>
  <dc:creator>Goss SL</dc:creator>
  <dc:creator>Rodila R</dc:creator>
  <dc:creator>Chen K</dc:creator>
  <dc:creator>Kupper H</dc:creator>
  <dc:creator>Kalabic J</dc:creator>
  <dc:date>2017</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">BACKGROUND
Treatment of rheumatoid arthritis (RA) with a combination of methotrexate (MTX)+adalimumab (ADA) is more effective than ADA monotherapy. We assessed the toxicity of different doses of MTX and treatment efficacy of ADA+MTX in two trials.


METHODS
Data originated from CONCERTO, in patients with early RA initiating ADA+ 2.5, 5, 10 or 20 mg/week MTX for 26 weeks; and MUSICA, in patients with an inadequate response to MTX initiating ADA+ 7.5 or 20 mg/week MTX for 24 weeks. Efficacy was assessed by the American College of Rheumatology 50 (ACR50). Patient-reported MTX-related toxicity information was collected at each visit on 18 prespecified MTX-related adverse events (AE) in the MTX label.


RESULTS
In CONCERTO, ACR50 rates increased over time, ranging from 54% to 68% at week 26, while AE rates remained steady, ranging from 2.4% to 17.8% at week 26. Of 395 patients, 113 (28.6%) reported 345 MTX-related AEs, including one serious AE (SAE, excessive fatigue and/or malaise); 10 AEs (in two patients) led to study discontinuation. In MUSICA, ACR50 rates increased over time, and were 32.3% and 37.5% at week 24, while MTX-related AE rates remained steady and were 6.5% at week 24. Of 309 patients, 71 (23%) reported 185 MTX-related AEs, including 5 SAEs (four infections and one fever/chills); six AEs (in four patients) led to study discontinuation.


CONCLUSION
In patients with RA initiating ADA+MTX combination, treatment efficacy was achieved and increased throughout both trials, while rates of MTX-related AEs remained steady. MTX-related AEs were observed in up to 30% of patients and most were mild. MTX was discontinued by 0.5%-1.3% of patients.


TRIAL REGISTRATION NUMBER
MUSICA (NCT01185288), CONCERTO (NCT01185301), Post results.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/232556</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1136/rmdopen-2017-000465</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/28955494</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>RMD open. - 2017</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">adalimumab</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">combination treatment</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">efficacy</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">methotrexate</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">rheumatoid arthritis</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">toxicity</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Treatment efficacy and methotrexate-related toxicity in patients with rheumatoid arthritis receiving methotrexate in combination with adalimumab.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
