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Editorial

Current and Emerging Treatment Options in Sinus and Nasal Diseases: A Promising Future in the Appropriate Therapies

1
Department of Otorhinolaryngology-Head and Neck Surgery, Huashan Hospital of Fudan University, Shanghai 200040, China
2
Department of Otorhinolaryngology & Clinical Allergy Center, The First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2022, 11(24), 7398; https://doi.org/10.3390/jcm11247398
Submission received: 8 December 2022 / Accepted: 10 December 2022 / Published: 14 December 2022
(This article belongs to the Special Issue Current and Emerging Treatment Options in Sinus and Nasal Diseases)
Chronic rhinosinusitis (CRS) is an inflammatory condition of the nose and paranasal sinuses defined by clinical symptoms, including two or more symptoms, one of which should be either nasal blockage or nasal discharge with or without facial pain/pressure or reduction in/loss of sense of smell. Most specialists require both symptoms and auxiliary examinations such as endoscopy and computed tomography to characterize the chronicity as lasting more than 12 weeks [1,2]. The prevalence of CRS is estimated to be 10–28% on the basis of self-reported investigations [3,4] and is approximately 4–9% after the above examinations [5,6,7].
Traditionally, CRS is classified as CRS with nasal polyps (CRSwNP) or without nasal polyps (CRSsNP) based on its phenotype. Now, primary CRS is identified as type 2 or non-type 2 condition according to its endotype [8]. The pivotal factors of type 2 CRS are T helper 2 (Th2) cells and innate lymphoid cells 2 (ILC2s) and their corresponding cytokine productions, including interleukin (IL)-4, IL-5 and IL-13. The increased specific immunoglobulin (Ig) E and eosinophilia in nasal mucosa also characterize the features of the type 2 inflammation [9]. The non-type 2 CRS comprises type 1 and type 3 inflammatory conditions, respectively. The former is mediated by Th1 and its characteristic cytokine interferon gamma (IFN-γ) and ILC1s, and the latter is induced by Th17 and its productions, such as IL-17, IL-22 and IL-23 [10].
With regards to the treatments of CRS, many otorhinolaryngologists suggest performing functional endoscopic sinus surgery (FESS) in order to open up the sinus ostia, drain the purulent discharge and remove nasal polyps after or concomitantly with the pharmacotherapy, such as intranasal corticosteroids (INCS), saline irrigation, antibiotics, allergen immunotherapy and biologics.
A large number of studies support the efficacy of INCS in the treatments of CRSwNP [11,12] and CRSsNP [13]. Agents such as mometasone furoate, budesonide, fluticasone furoate, fluticasone propionate, beclomethasone dipropionate and triamcinolone acetonide can all improve nasal symptoms, and there seem to be no obvious differences among these nasal sprays. INCS should be considered as the first-line therapy for CRS, especially for CRSwNP. As for oral corticosteroids, short courses of this medication can be considered a “medical polypectomy” similar to the surgical procedure in the treatment of CRSwNP [14]. However, a paucity of studies assess the efficacy of oral corticosteroids on nasal symptoms in patients with CRSsNP. Therefore, these agents should be used cautiously in these patients [15].
Nasal saline irrigation is considered to be an adjunctive therapy for CRSwNP or CRSsNP, whether before or after the endoscopic sinus surgery. This medical treatment has been proven to be effective in improving the clinical symptoms, at least through clearing secretions, and inflammatory mediators from the nasal mucosa and promoting mucociliary function in the nasal cavity and paranasal sinuses [16,17]. Relevant experts recommend that high-volume (>200 mL), properly hygienic and thermal, isotonic or hypertonic saline should be used for CRS patients.
Since CRS is not a primary infectious process, antimicrobial therapy is not the mainstream treatment. Some antimicrobials such as macrolide antibiotics and tetracyclines, which are found to have anti-inflammatory properties, may regulate this disease through nonantimicrobial mechanisms. Macrolide antibiotics are reported to have the capability of inhibiting IL-8 and tumor necrosis factor-α productions, downregulating the NF-κB signaling pathway and suppressing neutrophil functions. As a consequence, this agent has been proposed to treat CRSsNP [18,19,20]. However, the current data do not recommend the routine use of the antibiotics in patients with CRSwNP [21].
There is less evidence of efficacy of allergen immunotherapy in the treatment of CRSwNP and CRSsNP. This kind of therapy might not be suggested to be used for the improvement of sinus diseases even if some patients have concomitant allergic rhinitis [22,23].
CRSwNP is most often characterized by elevated local eosinophilia and pronounced infiltrates of Th2 cells and ILC2s [24,25,26] and their type 2 proinflammatory mediators [27], especially in Western countries. Relevant therapies such as biologics targeting type 2 inflammation have been deeply investigated and used to challenge the patients with type 2 CRS, especially eosinophilic CRSwNP.
Many biologics are monoclonal antibodies that are capable of targeting specific inflammatory cells or their mediators involved in the type 2 inflammatory condition [28]. Dupilumab can block IL-4 receptor (R) α, the shared R for both IL-4 and IL-13 signaling pathways, which can accordingly prevent the downstream cascade reactions in the specific immune system cells. This agent was approved by the U.S. Food and Drug Administration (FDA) to treat the difficult-to-control CRSwNP and was also approved to treat moderate-to-severe atopic dermatitis and refractory eosinophilic asthma in June 2019 [29]. Omalizumab is also a popular biologic; it is an anti-IgE monoclonal antibody that binds to free IgE in the blood circulation. It was approved by the FDA for the treatment of CRSwNP, which cannot be adequately controlled using INCS, and for moderate-to-severe persistent allergic asthma and chronic spontaneous urticaria in December 2020 [30]. Mepolizumab is a monoclonal anti-IL-5 antibody that can bind to circulating IL-5, which inhibits the IL-5 signaling pathway and thereby restrains the activation and recruitment of eosinophils. This biological agent was approved by the FDA as an adjunctive therapy for treating patients with CRSwNP in July 2021 [31] and was also approved to be used in the treatment of refractory eosinophilic asthma and EGPA (eosinophilic granulomatosis with polyangiitis) [32]. Benralizumab is a monoclonal anti-IL-5R antibody which was approved by the FDA to treat severe eosinophilic asthma. This agent has also been reported to reduce nasal polyps score, decrease nasal blockage and improve the sense of smell in CRSwNP patients [33]. Since several biologics are available for the therapeutic use for CRSwNP, clinicians must decide which one is appropriate for the individual case. However, no specific biomarkers have been identified to help decide the appropriate treatment using one biological vs. another. Future studies are required to better understand the specific biomarkers, thereby helping guide the clinical therapies and matching the patient’s personalized goals.
There are multiple possible treatment options for patients with CRS. Clinicians should identify which phenotype/endotype the individual patient has in his/her CRS condition based on medical history, endoscopy and computed tomography and a laboratory evaluation. Of course, other factors such as the patient’s preference and the cost and efficacy of the specific therapy should also be taken into consideration before commencing of the most appropriate therapy.
The current Special Issue invites authors to submit their original research including clinical and pre-clinical research papers related to the therapies of sinus and nasal diseases as well as the relevant review manuscripts. The Journal of Clinical Medicine also accepts studies showing meaningful but negative results, thereby encouraging scholars and scientists to share these data so that they would not repeat these experiments. We also sincerely hope that all our readers will enjoy this journal.

Author Contributions

L.L. wrote the manuscript, and L.C. checked and approved it carefully. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kaper, N.M.; van der Heijden, G.J.M.G.; Cuijpers, S.H.; Stokroos, R.J.; Aarts, M.C.J. A comparison of international clinical practice guidelines on adult chronic rhinosinusitis shows considerable variability of recommendations for diagnosis and treatment. Eur. Arch. Otorhinolaryngol. 2020, 277, 659–668. [Google Scholar] [CrossRef] [PubMed]
  2. Peters, A.T.; Spector, S.; Hsu, J.; Hamilos, D.L.; Baroody, F.M.; Chandra, R.K.; Grammer, L.C.; Kennedy, D.W.; Cohen, N.A.; Kaliner, M.A.; et al. Diagnosis and management of rhinosinusitis: A practice parameter update. Ann. Allergy Asthma Immunol. 2014, 113, 347–385. [Google Scholar] [CrossRef] [PubMed]
  3. Hastan, D.; Fokkens, W.J.; Bachert, C.; Newson, R.B.; Bislimovska, J.; Bockelbrink, A.; Bousquet, P.J.; Brozek, G.; Bruno, A.; Dahlén, S.E.; et al. Chronic rhinosinusitis in Europe—An underestimated disease. A GA2LEN study. Allergy 2011, 66, 1216–1223. [Google Scholar] [CrossRef] [PubMed]
  4. Ostovar, A.; Fokkens, W.J.; Vahdat, K.; Raeisi, A.; Mallahzadeh, A.; Farrokhi, S. Epidemiology of chronic rhinosinusitis in Bushehr, southwestern region of Iran: A GA2LEN study. Rhinology 2019, 57, 43–48. [Google Scholar] [CrossRef]
  5. Kim, J.H.; Cho, C.; Lee, E.J.; Suh, Y.S.; Choi, B.I.; Kim, K.S. Prevalence and risk factors of chronic rhinosinusitis in South Korea according to diagnostic criteria. Rhinology 2016, 54, 329–335. [Google Scholar] [CrossRef]
  6. Dietz de Loos, D.; Lourijsen, E.S.; Wildeman, M.A.M.; Freling, N.J.M.; Wolvers, M.D.J.; Reitsma, S.; Fokkens, W.J. Prevalence of chronic rhinosinusitis in the general population based on sinus radiology and symptomatology. J. Allergy Clin. Immunol. 2019, 143, 1207–1214. [Google Scholar] [CrossRef]
  7. Hirsch, A.G.; Nordberg, C.; Bandeen-Roche, K.; Tan, B.K.; Schleimer, R.P.; Kern, R.C.; Sundaresan, A.; Pinto, J.M.; Kennedy, T.L.; Greene, J.S.; et al. Radiologic sinus inflammation and symptoms of chronic rhinosinusitis in a population-based sample. Allergy 2020, 75, 911–920. [Google Scholar] [CrossRef]
  8. Fokkens, W.J.; Lund, V.J.; Hopkins, C.; Hellings, P.W.; Kern, R.; Reitsma, S.; Toppila-Salmi, S.; Bernal-Sprekelsen, M.; Mullol, J.; Alobid, I.; et al. European Position Paper on Rhinosinusitis and Nasal Polyps 2020. Rhinology 2020, 58, 1–464. [Google Scholar] [CrossRef]
  9. Asano, K.; Ueki, S.; Tamari, M.; Imoto, Y.; Fujieda, S.; Taniguchi, M. Adult-onset eosinophilic airway diseases. Allergy 2020, 75, 3087–3099. [Google Scholar] [CrossRef]
  10. Bachert, C.; Zhang, N. Medical algorithm: Diagnosis and treatment of chronic rhinosinusitis. Allergy 2020, 75, 240–242. [Google Scholar] [CrossRef]
  11. Orlandi, R.R.; Kingdom, T.T.; Smith, T.L.; Bleier, B.; DeConde, A.; Luong, A.U.; Poetker, D.M.; Soler, Z.; Welch, K.C.; Wise, S.K.; et al. International consensus statement on allergy and rhinology: Rhinosinusitis 2021. Int. Forum Allergy Rhinol. 2021, 11, 213–739. [Google Scholar]
  12. Chong, L.Y.; Head, K.; Hopkins, C.; Philpott, C.; Schilder, A.G.; Burton, M.J. Intranasal steroidsversus placebo or no intervention for chronic rhinosinusitis. Cochrane Database Syst. Rev. 2016, 4, CD011996. [Google Scholar] [PubMed] [Green Version]
  13. Snidvongs, K.; Kalish, L.; Sacks, R.; Craig, J.C.; Harvey, R.J. Topical steroid for chronic rhinosinusitis without polyps. Cochrane Database Syst. Rev. 2011, 10, CD009274. [Google Scholar]
  14. Zhang, Y.; Wang, C.; Huang, Y.; Lou, H.; Zhang, L. Efficacy of short-term systemic corticosteroid therapy in chronic rhinosinusitis with nasal polyps: A meta-analysis of randomized controlled trials and systematic review. Am. J. Rhinol. Allergy 2019, 33, 567–576. [Google Scholar] [CrossRef] [PubMed]
  15. Borish, L.; Baroody, F.M.; Kim, M.S.; Lieberman, J.A.; Peters, A.; Stevens, W.W.; Bernstein, J.A. Yardstick for the medical management of chronic rhinosinusitis. Ann. Allergy Asthma Immunol. 2022, 128, 118–128. [Google Scholar] [CrossRef] [PubMed]
  16. Chong, L.Y.; Head, K.; Hopkins, C.; Philpott, C.; Glew, S.; Scadding, G.; Burton, M.J.; Schilder, A.G. Saline irrigation for chronic rhinosinusitis. Cochrane Database Syst. Rev. 2016, 4, CD011995. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Succar, E.F.; Turner, J.H.; Chandra, R.K. Nasal saline irrigation: A clinical update. Int. Forum Allergy Rhinol. 2019, 9, S4–S8. [Google Scholar] [CrossRef] [Green Version]
  18. Lees, K.A.; Orlandi, R.R.; Oakley, G.; Alt, J.A. The role of macrolides and doxycycline in chronic rhinosinusitis. Immunol. Allergy Clin. North. Am. 2020, 40, 303–315. [Google Scholar] [CrossRef]
  19. Oakley, G.M.; Harvey, R.J.; Lund, V.J. The role of macrolides in chronic rhinosinusitis (CRSsNP and CRSwNP). Curr. Allergy Asthma Rep. 2017, 17, 30. [Google Scholar] [CrossRef]
  20. Huang, Z.; Zhou, B. Clarithromycin for the treatment of adult chronic rhinosinusitis: A systematic review and meta-analysis. Int. Forum Allergy Rhinol. 2019, 9, 545–555. [Google Scholar] [CrossRef]
  21. Fokkens, W.J. Long-term antibiotics for chronic rhinosinusitis: Changing views. Rhinology 2019, 57, 241. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. DeYoung, K.; Wentzel, J.L.; Schlosser, R.J.; Nguyen, S.A.; Soler, Z.M. Systematic review of immunotherapy for chronic rhinosinusitis. Am. J. Rhinol. Allergy 2014, 28, 145–150. [Google Scholar] [CrossRef] [PubMed]
  23. Nathan, R.A.; Santilli, J.; Rockwell, W.; Glassheim, J. Effectiveness of immunotherapy for recurring sinusitis associated with allergic rhinitis as assessed by the Sinusitis Outcomes Questionnaire. Ann. Allergy Asthma Immunol. 2004, 92, 668–672. [Google Scholar] [CrossRef] [PubMed]
  24. Kato, A. Immunopathology of chronic rhinosinusitis. Allergol. Int. 2015, 64, 121–130. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Poposki, J.A.; Klingler, A.I.; Tan, B.K.; Soroosh, P.; Banie, H.; Lewis, G.; Hulse, K.E.; Stevens, W.W.; Peters, A.T.; Grammer, L.C.; et al. Group 2 innate lymphoid cells are elevated and activated in chronic rhinosinusitis with nasal polyps. Immun. Inflamm. Dis. 2017, 5, 233–243. [Google Scholar] [CrossRef]
  26. Hulse, K.E.; Stevens, W.W.; Tan, B.K.; Schleimer, R.P. Pathogenesis of nasal polyposis. Clin. Exp. Allergy 2015, 45, 328–346. [Google Scholar] [CrossRef] [Green Version]
  27. Stevens, W.W.; Ocampo, C.J.; Berdnikovs, S.; Sakashita, M.; Mahdavinia, M.; Suh, L.; Takabayashi, T.; Norton, J.E.; Hulse, K.E.; Conley, D.B.; et al. Cytokines in chronic rhinosinusitis. Role in eosinophilia and aspirin-exacerbated respiratory disease. Am. J. Respir. Crit. Care Med. 2015, 192, 682–694. [Google Scholar] [CrossRef] [Green Version]
  28. Ren, L.; Zhang, N.; Zhang, L.; Bachert, C. Biologics for the treatment of chronic rhinosinusitis with nasal polyps—State of the art. World Allergy Organ. J. 2019, 12, 100050. [Google Scholar] [CrossRef] [Green Version]
  29. Laidlaw, T.M.; Mullol, J.; Fan, C.; Zhang, D.; Amin, N.; Khan, A.; Chao, J.; Mannent, L.P. Dupilumab improves nasal polyp burden and asthma control in patients with CRSwNP and AERD. J. Allergy ClinImmunol. Pract. 2019, 7, 2462–2465.e1. [Google Scholar] [CrossRef] [Green Version]
  30. Gevaert, P.; Omachi, T.A.; Corren, J.; Mullol, J.; Han, J.; Lee, S.E.; Kaufman, D.; Ligueros-Saylan, M.; Howard, M.; Zhu, R.; et al. Efficacy and safety of omalizumab in nasal polyposis: 2 randomized phase 3 trials. J. Allergy Clin. Immunol. 2020, 146, 595–605. [Google Scholar] [CrossRef]
  31. Han, J.K.; Bachert, C.; Fokkens, W.; Desrosiers, M.; Wagenmann, M.; Lee, S.E.; Smith, S.G.; Martin, N.; Mayer, B.; Yancey, S.W.; et al. Mepolizumab for chronic rhinosinusitis with nasal polyps (SYNAPSE): A randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Respir. Med. 2021, 9, 1141–1153. [Google Scholar] [CrossRef] [PubMed]
  32. Wechsler, M.E.; Akuthota, P.; Jayne, D.; Khoury, P.; Klion, A.; Langford, C.A.; Merkel, P.A.; Moosig, F.; Specks, U.; Cid, M.C.; et al. Mepolizumab or placebo for eosinophilic granulomatosis with polyangiitis. N. Engl. J. Med. 2017, 376, 1921–1932. [Google Scholar] [CrossRef] [PubMed]
  33. Bachert, C.; Han, J.K.; Desrosiers, M.Y.; Gevaert, P.; Heffler, E.; Hopkins, C.; Tversky, J.R.; Barker, P.; Cohen, D.; Emson, C.; et al. Efficacy and safety of benralizumab in chronic rhinosinusitis with nasal polyps: A randomized, placebo-controlled trial. J. Allergy Clin. Immunol. 2022, 149, 1309–1317.e12. [Google Scholar] [CrossRef] [PubMed]
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Lin, L.; Cheng, L. Current and Emerging Treatment Options in Sinus and Nasal Diseases: A Promising Future in the Appropriate Therapies. J. Clin. Med. 2022, 11, 7398. https://doi.org/10.3390/jcm11247398

AMA Style

Lin L, Cheng L. Current and Emerging Treatment Options in Sinus and Nasal Diseases: A Promising Future in the Appropriate Therapies. Journal of Clinical Medicine. 2022; 11(24):7398. https://doi.org/10.3390/jcm11247398

Chicago/Turabian Style

Lin, Lin, and Lei Cheng. 2022. "Current and Emerging Treatment Options in Sinus and Nasal Diseases: A Promising Future in the Appropriate Therapies" Journal of Clinical Medicine 11, no. 24: 7398. https://doi.org/10.3390/jcm11247398

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