Predictability Studies on the Efficacy of TNF-α Inhibitors in Chinese RA From "Real World"

Rheumatoid Arthritis Clinical Trial

Official title:

Screening Protein Predictive of Response to Tumor Necrosis Factor-α Inhibitors Treatment in Chinese Rheumatoid Arthritis From "Real World" and Investigating Its Mechanism Through Signal Pathway

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT02878161
• Other study ID #: XYEYY-GZ81571599-20160118-1
• Status: Enrolling by invitation
• Phase: Phase 4
• First received: July 12, 2016
• Last updated: August 21, 2016
• Start date: January 2016
• Est. completion date: December 2019

Study information

• Verified date: July 2016
• Source: Central South University
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Rheumatoid arthritis (RA) is a chronic and disabling disease. tumor necrosis factor-a(TNF-a) inhibitors have demonstrated an outstanding performance in relieving joint inflammation and retarding bone erosion involved in RA. However, there is still about one-thirds of RA patients had a poor response to TNF α inhibitors. The Investigators hope to discover prediction protein with a domestic genetic background and finally establish prediction system with Chinese characteristics.

Description:

Rheumatoid arthritis (RA) is a chronic and disabling disease. TNF-α inhibitors have demonstrated an outstanding performance in relieving joint inflammation and retarding bone erosion involved in RA. However, there is still about one-thirds of RA patients had a poor response to TNF α inhibitors. Currently the personalized biological treatment is the research hotspot. Recent studies focuses on exploring biomarkers predictive of drug response. The research methods such as genomics, transcriptomics, proteomics, metabolomics and immunocytology, have been applied,but they are not successfully integrated. The related studies in China are still at an initial stage, which necessitates an in-depth study in this area. The investigators' preliminary study showed that TNF-α-308 gene polymorphisms existed in Chinese RA patients and phosphoinositide 3-kinase/Akt signal pathway was activated in proliferated synovial fibroblasts stimulated by TNF-α. Therefore, for the first attempt in China, the investigators intend to screen for differential proteins by using isobaric tags for relative and absolute quantitation(iTRAQ) technique in RA patients receiving anti-TNF-α therapy, and then verify the predictive effects of selected differential proteins from the upstream gene polymorphism to the downstream protein expression. The investigators will also explore the mechanisms of differential proteins involved in TNF-α related signal pathway by using in vitro gene transfer, siRNA interference, and RA animal models. Through this study investigator hope to discover some prediction proteins with a domestic genetic background and finally establish a prediction system with Chinese characteristics.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 240
• Est. completion date: December 2019
• Est. primary completion date: December 2019
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• signed the consents voluntarily

• age between 18-75 years old

• patients were meet the American College of Rheumatology(ACR)

• European League Against Rheumatism(EULAR) 2009 diagnostic criteria (total scores beyond 6)

• for severe RA patients DAS28-CRP=5.1

• The participants receiving Infliximab plus Methotrexate will be invited to enroll the study.

• The participants receiving Etanercept plus Methotrexate will be invited to enroll the study.

• The participants receiving Adalimumab plus Methotrexate will be invited to enroll the study.

Exclusion Criteria:

• The patient have the disease history or the disease of cardiovascular, respiratory system, liver, gastrointestinal tract, endocrine, hematology, neurology or psychiatric disturbance, and investigator believe that there are some risks for patients with these disease history or disease when use study drugs, or these disease history or disease will disturb the interpret of data

• Patients with cancer in situ or exist the possibility of cancer malignancies

• Basically or completely loss of mobility, lack self-care ability, such as rely on a wheelchair or bed-ridden .

• Experimental examination display any of the following:

Aspartate aminotransferase or alanine aminotransferase>1.5 times of the upper limit of the normal value Total bilirubin>1.5 times of the upper limit of the normal value Total white blood cells <2500 cells/L absolute neutrophil count <1200 cells/L lymphocyte count <750 cells/L platelet<100000/L

• Patients with symptomatic herpes simplex

• Latent tuberculosis signal (PPD+++ OR T-SPOT>5 )

• Positive result of the hepatitis B virus (HBV):

HBsAg + Or HBeAg + Or HBeAg + Or HBcAb + Or HBV DNA +

• hepatitis C virus(HCV)+ or HCV RNA +

• HIV infection or HIV+

• 1 months before join the group, from a clinical point of view,patients have a serious infection caused by the virus, bacteria, fungi, or parasites

• Pregnancy ? location ?prepare for conceive in one years or there is risk to impregnate their partners

• Patients received any biological therapies for 6 months, or participated any other clinical trials of new drugs

• A history of drug allergy

• A history of heavy drink

• vaccinate the live vaccine recently

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Arthritis
• Arthritis, Rheumatoid
• Rheumatoid Arthritis

Intervention

Drug:
• methotrexate(necessary)
Methotrexate will be received orally with dosage of 10mg/ week for every patient and MTX dose must be stable for at least 4 weeks.

Biological:
• infliximab
infliximab :intravenous injection 200mg,every times,0,2,6,14week ,4 times)
• etanercept
Etanercept :hypodermic injection,25mg/twice a week
• adalimumab
Adalimumab:hypodermic injection,40mg/twice a week

Drug:
• leflunomide (permitted, not necessary)
LEF will be permitted if patient had received for 1 month before enrollment and will not be changed for 14 weeks.
• NSAIDs (permitted,not necessary)
NSAIDs will be allowed if patient had received for 1 month before enrollment and will not be changed for 14 weeks.
• Glucocorticoids (permitted,not necessary)
Glucocorticoids (prednisone less than 10mg/day, or equal dosage of other similar drugs) will be permitted if the patient had received for 1 month before enrollment and the dosage will not be changed during the period.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Fen Li

References & Publications (43)

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* Note: There are 43 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	EULAR (European League Against Rheumatism) response will be assessed among patients of 3 groups	EULAR (European League Against Rheumatism) response is based on changes of DAS28-CRP. The following good, moderate and no response are defined based on changes of DAS28-CRP from baseline to weeks 14: >1.2 units are good response; 0.6-1.2 units are moderate response; =0.6 units are no response.; The DAS28-CRP will be calculated at every visit within the clinical database. The components of the DAS28-CRP score assessment are: Tender/Painful Joint Count (28); Swollen Joint Count (28), hsCRP, and the Subject General Health VAS assessment. This efficacy measurement will be made at baseline and weeks 14.	Baseline, Weeks 14	No
Secondary	The changes of TNF level with different EULAR response will be assessed among patients of 3 groups.	The TNF level assessment is a direct measurement using ELISA by testing patients' serum. This measurement will be made at baseline and weeks 14.; The classification of EULAR response and the calculation of DAS28-CRP are based on above of Primary Outcome Measure.	Baseline, Weeks 14	No
Secondary	The changes of Interest proteins with different EULAR response will be assessed among patients of 3 group.	Interest proteins will be screened by iTRAQ (isobaric tags for relative and absolute quantitation). This measurement will be made at baseline and weeks 14 by comparing part of patients with good response or no response.; Interest proteins being screened will be verified by Western Blot among all patients of 3 groups.; The classification of EULAR response and the calculation of DAS28-CRP are based on above of Primary Outcome Measure.	Baseline, Weeks 14	No
Secondary	The SNP (Single nucleotide polymorphism) of gene about TNF with different EULAR response will be assessed among patients of 3 groups.	SNP of TNF gene will be tested by PCR-RFLP (Polymerase Chain Reaction -Restriction Fragment Length Polymorphism). This measurement will be made at weeks 14 among all 3 groups' patients.; The classification of EULAR response and the calculation of DAS28-CRP are based on above of Primary Outcome Measure.	Weeks 14	No
Secondary	The SNP of gene about interest proteins with different EULAR response will be assessed among patients of 3 groups.	SNP of gene about interest proteins will tested by PCR-HRM(Polymerase Chain Reaction-high resolution melting). This measurement will be made at weeks 14 among all 3 groups' patients.; Interest proteins are screened and verified on above of Secondary Outcome Measure.; The classification of EULAR response and the calculation of DAS28-CRP are based on above of Primary Outcome Measure.	Weeks 14	No