Monoclonal antibodies in severe asthma: is it worth it?
被引:10
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作者:
Calzetta, Luigino
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Univ Roma Tor Vergata, Dept Expt Med, Unit Resp Med, Rome, Italy
Univ Catanzaro Magna Graecia, Dept Hlth Sci, Catanzaro, ItalyUniv Roma Tor Vergata, Dept Expt Med, Unit Resp Med, Rome, Italy
Calzetta, Luigino
[1
,2
]
Matera, Maria Gabriella
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Univ Campania Luigi Vanvitelli, Dept Expt Med, Unit Pharmacol, Naples, ItalyUniv Roma Tor Vergata, Dept Expt Med, Unit Resp Med, Rome, Italy
Matera, Maria Gabriella
[3
]
Rogliani, Paola
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Univ Roma Tor Vergata, Dept Expt Med, Unit Resp Med, Rome, ItalyUniv Roma Tor Vergata, Dept Expt Med, Unit Resp Med, Rome, Italy
Rogliani, Paola
[1
]
机构:
[1] Univ Roma Tor Vergata, Dept Expt Med, Unit Resp Med, Rome, Italy
[2] Univ Catanzaro Magna Graecia, Dept Hlth Sci, Catanzaro, Italy
[3] Univ Campania Luigi Vanvitelli, Dept Expt Med, Unit Pharmacol, Naples, Italy
Background: To date, there is the strong need to compare the efficacy across the monoclonal antibodies (mAbs) approved to treat severe asthma. Research design and method: A quantitative synthesis has been performed to compare the impact of omalizumab, mepolizumab, reslizumab, benralizumab, dupilumab, and placebo on the risk of exacerbation and change in forced expiratory flow in 1 s (FEV1) in severe asthmatic patients. Results: All the investigated mAbs were more effective than placebo in reducing the risk of exacerbation and improving lung function. Dupilumab showed a general superiority compared to the other mAbs, as it significantly reduced the risk of exacerbation vs. omalizumab, and significantly improved FEV1 when compared to omalizumab, mepolizumab, and benralizumab. The overall-marked placebo effect indicates that a better adherence to drug regimens in the context of RCTs may lead to noteworthy improvement in the clinical condition of severe asthmatic patients. Conclusions: Further extensive meta-analyses are needed to identify the factors influencing the efficacy profile of mAbs in severe asthma. This may also permit to identify the profile of patients that are specifically responsive to either anti-IgE, anti-IL-4R alpha, anti-IL-5, or anti-IL-5R alpha mAbs.
机构:
Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Rheumatol Allergy & Immunol, Boston, MA 02114 USAHarvard Univ, Massachusetts Gen Hosp, Sch Med, Div Rheumatol Allergy & Immunol, Boston, MA 02114 USA
机构:
Ferris State Univ, Pharm Practice, Coll Pharm, 418 West Magnetic St, Marquette, MI 49855 USAFerris State Univ, Pharm Practice, Coll Pharm, 418 West Magnetic St, Marquette, MI 49855 USA
Koski, Renee R.
Grzegorczyk, Kirsten M.
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Walgreens, Big Rapids, MI USAFerris State Univ, Pharm Practice, Coll Pharm, 418 West Magnetic St, Marquette, MI 49855 USA
机构:
Harvard Med Sch, Brigham & Womens Hosp, Partners Asthma Ctr, Pulm & Crit Care Med Div, PBB Clin 3 75 Francis St, Boston, MA 02115 USAHarvard Med Sch, Brigham & Womens Hosp, Partners Asthma Ctr, Pulm & Crit Care Med Div, PBB Clin 3 75 Francis St, Boston, MA 02115 USA
机构:
Univ Roma Tor Vergata, Dept Expt Med & Surg, Unit Resp Med, Rome, ItalyUniv Roma Tor Vergata, Dept Expt Med & Surg, Unit Resp Med, Rome, Italy
Cazzola, Mario
Matera, Maria Gabriella
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Univ Campania Luigi Vanvitelli, Dept Expt Med, Unit Pharmacol, Naples, ItalyUniv Roma Tor Vergata, Dept Expt Med & Surg, Unit Resp Med, Rome, Italy
Matera, Maria Gabriella
Levi-Schaffer, Francesca
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Hebrew Univ Jerusalem, Fac Med, Inst Drug Res, Sch Pharm,Pharmacol & Expt Therapeut Unit, Jerusalem, IsraelUniv Roma Tor Vergata, Dept Expt Med & Surg, Unit Resp Med, Rome, Italy
Levi-Schaffer, Francesca
Rogliani, Paola
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Univ Roma Tor Vergata, Dept Expt Med & Surg, Unit Resp Med, Rome, ItalyUniv Roma Tor Vergata, Dept Expt Med & Surg, Unit Resp Med, Rome, Italy