Session Information
Session Type: ACR Poster Session C
Session Time: 9:00AM-11:00AM
Background/Purpose: Rheumatoid arthritis (RA) patients frequently report concomitant comorbidities that could worsen their prognosis. Tumor necrosis factor inhibitors (TNFi), the most common biological agents used, have shown efficacy in RA patients, although use in RA patients with certain comorbidities warrant caution (1). Abatacept, a biologic agent with a different mechanism of action, inhibiting the co-stimulation of the T-lymphocyte, has demonstrated differentiated safety profile (2), that could influence the biological agent prescribed in RA patients with some associated comorbidities. Our objective is to analyze differences in the frequency of baseline comorbidities in RA patients treated with abatacept compared with those treated with TNFi
Methods: Patients with RA recruited into the BIOBADASER 2.0 register from January 2008 to December 2014 and treated with abatacept or TNFi with comorbidities were selected. Comorbidity was defined as ≥ 1 of the following at initiation of biological therapy: Ischemic heart disease; lymphoma; malignancy (except lymphoma); diabetes; chronic pulmonary obstructive disease (CPOD); smoking; hypercholesterolemia; hypertension; heart failure; renal failure; osteoporosis; Epstein Barr, hepatitis B or C virus infection; and others. We analyzed the frequency of each comorbiditiy and the differences in the rate of baseline comorbidities between the two groups
Results: From January 2008 to December 2014, 640 and 252 RA patients treated respectively with TNFi or abatacept, were included in the BIOBADASER 2.0 register, of whom 51.6% had ≥ 1 comorbitity at baseline. Frequencies for every basal comorbidity described ere shown in Table 1. There was a significantly higher rate of heart failure in abatacept than in TNFi patients. Other comorbidities showed no significant differences Table 1
Frequency (%) |
|||
Comorbidities |
Abatacept |
TNFi |
p-value |
Ischemic heart disease |
1(2.3) |
14(2.1) |
0.940 |
Malignancy (except lymphoma) |
1(2.3) |
13(1.9) |
0.883 |
Diabetes |
6(13.6) |
46(6.9) |
0.098 |
CPOD |
2(4.6) |
16(2.4) |
0.382 |
Smoking |
8(18.2) |
109(16.4) |
0.757 |
Hypercholesterolemia |
9(20.4) |
111(16.7) |
0.519 |
Hypertension |
10(22.7) |
148(22.3) |
0.942 |
Epstein Barr infection |
0(0) |
1(0.1) |
0.797 |
Heart failure |
4(9.1) |
6(0.9) |
<0.001 |
Renal failure |
0(0) |
8(1.2) |
0.464 |
Lymphoma |
0(0) |
0(0) |
|
Osteoporosis |
7(15.9) |
89(13.4) |
0.635 |
Hepatitis B virus infection |
1(2.3) |
13(1.9) |
0.883 |
Hepatitis C virus infection |
0(0) |
1(0.1) |
0.797 |
Others |
22(50) |
292(43.9) |
0.431 |
Conclusion: RA patients treated with abatacept had a higher baseline frequency of concomitant heart failure compared with patients treated with TNFi, probably reflecting different recommendations on biological drug use. No differences in other baseline comorbidities were found between groups References: (1) Singh et al. Arthritis Rheum 2016; 68: 1–26. (2) Singh et al. Cochrane Database Syst Rev. 2011; 16: CD008794
To cite this abstract in AMA style:
Hernández MV, Sánchez-Piedra C, Inciarte-Mundo J, Sanchez-Alonso F, Manero J, Roselló R, Pérez-Pampin E, Rodriguez-Lozano C, Diaz-Torné C, Sanmarti R, Gómez-Reino JJ. Are There Differences in Baseline Comorbidities Between Rheumatoid Arthritis Patients Treated with Abatacept and Those Treated with Tumor Necrosis Factor Inhibitors? [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/are-there-differences-in-baseline-comorbidities-between-rheumatoid-arthritis-patients-treated-with-abatacept-and-those-treated-with-tumor-necrosis-factor-inhibitors/. Accessed .« Back to 2016 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/are-there-differences-in-baseline-comorbidities-between-rheumatoid-arthritis-patients-treated-with-abatacept-and-those-treated-with-tumor-necrosis-factor-inhibitors/