Treatment of Bullous Pemphigoid in People Aged 80 Years and Older: A Systematic Review of the Literature

被引:6
作者
Oren-Shabtai, Meital [1 ,2 ]
Kremer, Noa [1 ,2 ]
Lapidoth, Moshe [1 ,2 ]
Sharon, Eran [2 ,3 ]
Atzmony, Lihi [1 ,2 ]
Nosrati, Adi [1 ,2 ]
Hodak, Emmilia [1 ,2 ]
Mimouni, Daniel [1 ,2 ]
Levi, Assi [1 ,2 ]
机构
[1] Rabin Med Ctr, Div Dermatol, 39 Zeev Jabotinsky St, IL-4941492 Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
[3] Beilinson Med Ctr, Dept Surg, Breast Surg Clin, Rabin Med Ctr, Petah Tiqwa, Israel
关键词
LOW-DOSE METHOTREXATE; TOPICAL CORTICOSTEROIDS; THERAPEUTIC OPTION; ELDERLY-PATIENTS; MORTALITY; AUTOANTIBODIES; MULTICENTER; MANAGEMENT; RISK; ASSOCIATIONS;
D O I
10.1007/s40266-020-00823-5
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background Bullous pemphigoid commonly affects older adults and has a detrimental effect on both quality of life and longevity. Systemic corticosteroids, the mainstay of therapy, may cause significant adverse effects, especially in older patients. Therefore, safer therapeutic options are being sought. Objective The objective of this article was to systematically review the published evidence on the efficacy and safety of different treatment modalities for bullous pemphigoid in older patients. Methods We performed a systematic review of all publications until May 2020 in PubMed, Google Scholar, and the ongoing trials registry of the US National Institutes of Health databases evaluating the efficacy and safety of bullous pemphigoid treatments in patients aged older than 80 years. The primary outcome was complete response. The secondary outcomes were partial response, complete remission on minimal therapy or during tapering, recurrence, adverse events, and mortality. Results Twenty-eight publications were included: 2 randomized controlled trials, 5 prospective cohort studies, 10 retrospective cohort studies, and 11 case series, with a total of 153 older patients. The overall complete response rate was 31%. Topical corticosteroids had the highest complete response rate (55%) with a low side-effect profile. Biologics (omalizumab and rituximab) were effective in achieving complete remission on minimal therapy (29%) without recurrence, although rituximab was associated with a relatively high mortality rate (29%). Conclusions Current data suggest that topical corticosteroids are effective and safe and should remain the first line of treatment for bullous pemphigoid in older adults. However, their application is difficult and requires a high-functioning patient, third-party assistance, or a relatively mild disease. Biological agents are effective but warrant meticulous patient selection owing to the relatively high mortality rate associated with rituximab.
引用
收藏
页码:125 / 136
页数:12
相关论文
共 64 条
[11]   Neurological disorders in patients with bullous pemphigoid [J].
Cordel, Nadege ;
Chosidow, Olivier ;
Hellot, Marie-France ;
Delaporte, Emmanuel ;
Lok, Catherine ;
Vaillant, Loic ;
Bernard, Philippe ;
D'Incan, Michel ;
Roujeau, Jean Claude ;
Joly, Pascal .
DERMATOLOGY, 2007, 215 (03) :187-191
[12]   Evidence-Based Management of Bullous Pemphigoid [J].
Daniel, Benjamin S. ;
Borradori, Luca ;
Hall, Russell P., III ;
Murrell, Dedee F. .
DERMATOLOGIC CLINICS, 2011, 29 (04) :613-+
[13]   Treatment of bullous pemphigoid by low-dose methotrexate associated with short-term potent topical steroids: Aan open prospective study of 18 cases [J].
Dereure, O ;
Bessis, D .
ARCHIVES OF DERMATOLOGY, 2002, 138 (09) :1255-1256
[14]   Combined treatment with low-dose methotrexate and initial short-term superpotent topical steroids in bullous pemphigoid: an open, multicentre, retrospective study [J].
Du-Thanh, A. ;
Merlet, S. ;
Maillard, H. ;
Bernard, P. ;
Joly, P. ;
Esteve, E. ;
Richard, M. A. ;
Pauwels, C. ;
Ingen-Housz-Oro, S. ;
Guillot, B. ;
Dereure, O. .
BRITISH JOURNAL OF DERMATOLOGY, 2011, 165 (06) :1337-1343
[15]   Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology [J].
Feliciani, C. ;
Joly, P. ;
Jonkman, M. F. ;
Zambruno, G. ;
Zillikens, D. ;
Ioannides, D. ;
Kowalewski, C. ;
Jedlickova, H. ;
Karpati, S. ;
Marinovic, B. ;
Mimouni, D. ;
Uzun, S. ;
Yayli, S. ;
Hertl, M. ;
Borradori, L. .
BRITISH JOURNAL OF DERMATOLOGY, 2015, 172 (04) :867-877
[16]   Clinical and Immunologic Factors Associated With Bullous Pemphigoid Relapse During the First Year of Treatment A Multicenter, Prospective Study [J].
Fichel, Fanny ;
Barbe, Coralie ;
Joly, Pascal ;
Bedane, Christophe ;
Vabres, Pierre ;
Truchetet, Francois ;
Aubin, Francois ;
Michel, Catherine ;
Jegou, Juliette ;
Grange, Florent ;
Antonicelli, Frank ;
Bernard, Philippe .
JAMA DERMATOLOGY, 2014, 150 (01) :25-33
[17]   NICOTINAMIDE AND TETRACYCLINE THERAPY OF BULLOUS PEMPHIGOID [J].
FIVENSON, DP ;
BRENEMAN, DL ;
ROSAN, GB ;
HERSH, CS ;
CARDONE, S ;
MUTASIM, D .
ARCHIVES OF DERMATOLOGY, 1994, 130 (06) :753-758
[18]   Corticosteroid Use in Autoimmune Blistering Diseases [J].
Frew, John W. ;
Murrell, Dedee F. .
IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2012, 32 (02) :283-+
[19]   Mycophenolate mofetil:: A new therapeutic option in the treatment of blistering autoimmune diseases [J].
Grundmann-Kollmann, M ;
Korting, HC ;
Behrens, S ;
Kaskel, P ;
Leiter, U ;
Krähn, G ;
Kerscher, M ;
Peter, RU .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1999, 40 (06) :957-960
[20]   Treatment of bullous pemphigoid with low- dose oral cyclophosphamide: a case series of 20 patients [J].
Gual, A. ;
Iranzo, P. ;
Mascaro, J. M., Jr. .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2014, 28 (06) :814-818