Real-life biomarker response to anti-IL5 and anti-IgE therapies in severe asthma patients

S. Burkill (Singapore, Singapore), C. M. Porsbjerg (Bispebjerg, Denmark), A. Bourdin (Montpellier, France), T. N Tran (Gaithersburg, United States), N. Martin (Gaithersburg, United States), R. Katial (Gaithersburg, United States), P. Barker (Gaithersburg, United States), M. E Wechsler (Denver, United States), J. Maspero (Buenos Aires, Argentina), S. Bosnic-Anticevich (Sydney, Australia), L. Chung (Perth, Australia), G. Katsoulotos (Sydney, Australia), G. C Christoff (Sofia, Bulgaria), T. A Popov (Sofia, Bulgaria), M. Sadatsafavi (Vancouver, Canada), C. A Torres-Duque (Bogotá, Colombia), C. Ulrik (Hvidovre, Denmark), K. Dahl Assing (Aalborg, Denmark), S. Hansen (Copenhagen, Denmark), A. Altraja (Tartu, Estonia), L. A Lehtimaki (Tampere, Finland), N. G Papadopoulos (Athens, Greece), K. Kostikas (Ioannina, Greece), S. Salvi (Pune, India), R. W Costello (Dublin, Ireland), P. Francesca (Rozzano, Italy), T. Iwanaga (Osakasayama, Japan), C. Rhee (Seoul, Republic of Korea), M. Al-Ahmad (Kuwait, Kuwait), D. Larenas-Linnemann (Ciudad de México, Mexico), J. A Fonseca (Porto, Portugal), R. Amaral (Sweden, Sweden), K. Alving (Sweden, Sweden), R. Al-Lehebi (Riyadh, Saudi Arabia), L. Perez De-Llano (Monforte, Cervo, Italy), B. Kirenga (Kampala, Uganda), M. Tsai (Taiwan, Taiwan), B. Mahboub (Sharjah, United Arab Emirates), P. E Pfeffer (London, United Kingdom), W. Henley (Singapore, Singapore), Y. Liu (Brisbane, Australia), J. Lyu (Singapore, Singapore), C. Goh (Singapore, Singapore), T. Uthaman (Singapore, Singapore), D. Price (Singapore, Singapore), J. Townend (Norwich, United Kingdom)

Source: International Congress 2022 – Studies targeting IL-5 pathways in asthma
Session: Studies targeting IL-5 pathways in asthma
Session type: Thematic Poster
Number: 2136

Congress or journal article abstractE-poster

Abstract

Introduction/Background: Biologics (Bx) are known to decrease specific biomarker levels: anti-IL5 reduces blood eosinophils (BEC) and anti-IgE slightly reduces FeNO. Anti-IL5 and anti-IgE are thought to have limited effect on total IgE (IgE).

Aims and Objectives: To assess the proportions of severe asthma patients whose biomarkers (BEC, FeNO, and serum IgE) decrease following anti-IL5 and anti-IgE initiation.

Methods: Patients in the International Severe Asthma Registry (ISAR) with biomarker and Bx data were included. From pre-Bx baseline to the post-Bx time period, the median (IQR) change in biomarker level and the proportion of patients with >25% decrease in biomarkers were determined.

Results: At 2-3 years from Bx initiation, BEC decreased by >25% in 80.7% of anti-IL5 and 41.6% of anti-IgE patients. FeNO decreased by >25% in 41.6% of anti-IL5 and 47.8% of anti-IgE patients. IgE decreased by >25% in 41.7% of anti-IL5 and 15.6% of anti-IgE patients (Figure).

Figure: Median (IQR) biomarker changes and patient proportions with decreased biomarkers in response to Bx.

Conclusions: Anti-IL5 was superior in decreasing BEC and both Bx classes decreased FeNO to a limited extent. The lower proportion of anti-IgE patients with IgE reduction could be attributed to serum total IgE (not free IgE) measurement. Apart from anti-IL5’s effect on BEC, <50% patients had decreased biomarkers; the clinical implications should be explored.



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Citations should be made in the following way:
S. Burkill (Singapore, Singapore), C. M. Porsbjerg (Bispebjerg, Denmark), A. Bourdin (Montpellier, France), T. N Tran (Gaithersburg, United States), N. Martin (Gaithersburg, United States), R. Katial (Gaithersburg, United States), P. Barker (Gaithersburg, United States), M. E Wechsler (Denver, United States), J. Maspero (Buenos Aires, Argentina), S. Bosnic-Anticevich (Sydney, Australia), L. Chung (Perth, Australia), G. Katsoulotos (Sydney, Australia), G. C Christoff (Sofia, Bulgaria), T. A Popov (Sofia, Bulgaria), M. Sadatsafavi (Vancouver, Canada), C. A Torres-Duque (Bogotá, Colombia), C. Ulrik (Hvidovre, Denmark), K. Dahl Assing (Aalborg, Denmark), S. Hansen (Copenhagen, Denmark), A. Altraja (Tartu, Estonia), L. A Lehtimaki (Tampere, Finland), N. G Papadopoulos (Athens, Greece), K. Kostikas (Ioannina, Greece), S. Salvi (Pune, India), R. W Costello (Dublin, Ireland), P. Francesca (Rozzano, Italy), T. Iwanaga (Osakasayama, Japan), C. Rhee (Seoul, Republic of Korea), M. Al-Ahmad (Kuwait, Kuwait), D. Larenas-Linnemann (Ciudad de México, Mexico), J. A Fonseca (Porto, Portugal), R. Amaral (Sweden, Sweden), K. Alving (Sweden, Sweden), R. Al-Lehebi (Riyadh, Saudi Arabia), L. Perez De-Llano (Monforte, Cervo, Italy), B. Kirenga (Kampala, Uganda), M. Tsai (Taiwan, Taiwan), B. Mahboub (Sharjah, United Arab Emirates), P. E Pfeffer (London, United Kingdom), W. Henley (Singapore, Singapore), Y. Liu (Brisbane, Australia), J. Lyu (Singapore, Singapore), C. Goh (Singapore, Singapore), T. Uthaman (Singapore, Singapore), D. Price (Singapore, Singapore), J. Townend (Norwich, United Kingdom). Real-life biomarker response to anti-IL5 and anti-IgE therapies in severe asthma patients. 2136

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