Cutaneous Immune-Related Adverse Events Secondary to Immune Checkpoint Inhibitors and Their Management DOI

John M. Pach,

Jonathan S. Leventhal

Critical Reviews in Immunology, Год журнала: 2022, Номер 42(4), С. 1 - 20

Опубликована: Янв. 1, 2022

Immune checkpoint inhibitors (CPIs) are highly effective in the treatment of various cancers. Immunotherapy enhances antitumor activity by relieving inhibition T cells responsible for immune surveillance. However, overactivation leads to immune-related adverse events (irAE), which cutaneous most common. Examples include pruritus and maculopapular eruption commonly, psoriasis bullous dermatoses less and, rarely, severe, life-threatening eruptions such as Stevens-Johnson Syndrome or Toxic Epidermal Necrolysis. Many these autoimmune nature, may present <i>de novo</i> recurrence pre-existing disease. In order maximize therapeutic potential CPIs, it is essential recognize effectively manage irAE, can otherwise lead interruption discontinuation. This review summarizes presentation management dermatologic secondary dysregulation a result inhibitor therapy, including common (maculopapular eruption, pruritus, lichenoid dermatitis, vitiligo), (psoriasis, pemphigoid, erythema multiforme, eczematous alopecia areata, granulo-matous neutrophilic dermatoses), severe (acute generalized exanthematous pustulosis &#91;AGEP&#93;, drug reaction with eosinophilia systemic symptoms &#91;DRESS&#93;, syndrome toxic epidermal necrolysis &#91;SJS/TEN&#93;), well exacerbation disease (subacute lupus erythematosus, dermatomyositis, eosinophilic fasciitis, leukocytoclastic vasculitis, scleroderma-like reaction).

Язык: Английский

The effects of glucocorticoids and immunosuppressants on cancer outcomes in checkpoint inhibitor therapy DOI Creative Commons
Sebastian Bruera, María E. Suarez‐Almazor

Frontiers in Oncology, Год журнала: 2022, Номер 12

Опубликована: Авг. 23, 2022

The emergence of checkpoint inhibitors has created a paradigm shift for the treatment various malignancies. However, although these therapies are associated with improved survival rates, they also carry risk immune-related adverse events (irAEs). Moderate to severe irAEs typically treated glucocorticoids, sometimes addition immunosuppressants as steroid-sparing therapy. it is unclear how glucocorticoids and may impact cancer efficacy immune therapy on cancer. In this narrative review, we discuss effects including methotrexate, hydroxychloroquine, azathioprine, mycophenolate mofetil, tumor-necrosis factor (TNF)-inhibitors, interleukin-6 inhibitors, interleukin-1 abatacept, rituximab, Janus kinase (JAKi) cancer-specific outcomes in setting inhibitor use.

Язык: Английский

Процитировано

30

Immune-related adverse events in checkpoint blockade: Observations from human tissue and therapeutic considerations DOI Creative Commons

Kristian C. Williams,

Abigail Gault, Amy E. Anderson

и другие.

Frontiers in Immunology, Год журнала: 2023, Номер 14

Опубликована: Янв. 26, 2023

Checkpoint inhibitors (CPIs) are monoclonal antibodies which, by disrupting interactions of immune checkpoint molecules with their ligands, block regulatory signals otherwise exploited cancers. Despite revolutionary clinical benefits, CPI use is associated an array immune-related adverse events (irAEs) that mirror spontaneous autoreactivity. Severe irAEs necessitate pausing or stopping therapy and corticosteroids and/or other immunomodulatory interventions. increasingly widespread use, irAE pathobiology remains poorly understood; its elucidation may point to targeted mitigation strategies uncover predictive biomarkers for onset in patients, whilst casting new light on mechanisms immune-mediated disease. This review focuses common CPI-induced the gut, skin synovial joints, how these compare diseases such as ulcerative colitis, vitiligo inflammatory arthritis. We current understanding immunological changes reported following at level peripheral blood tissue. Many studies highlight dysregulation cytokines irAE-affected tissue, particularly IFNγ TNF. IrAE-affected tissues also predominantly infiltrated T-cells, low B-cell infiltration. Whilst there variability between studies, patients treated anti-programmed cell death-1 (PD-1)/PDL-1 therapies seem exhibit CD8+ T-cell dominance, CD4+ T-cells dominating those anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) monotherapy. Interestingly, CD8+CXCR3+ have been be elevated gastrointestinal, dermatological musculoskeletal -irAE affected tissues. These findings potential opportunities therapeutic development re-deployment existing prevent improve outcome irAEs.

Язык: Английский

Процитировано

18

The Use of Biologic Agents for the Treatment of Cutaneous Immune-Related Adverse Events from Immune Checkpoint Inhibitors: A Review of Reported Cases DOI
Jolanta Pach, Kailyn Valido, Annika Belzer

и другие.

American Journal of Clinical Dermatology, Год журнала: 2024, Номер 25(4), С. 595 - 607

Опубликована: Май 20, 2024

Язык: Английский

Процитировано

7

Immune Checkpoint Inhibitor-Induced Psoriasis DOI
Jolanta Pach,

Nina Mbonu,

Shaman Bhullar

и другие.

Dermatologic Clinics, Год журнала: 2024, Номер 42(3), С. 481 - 493

Опубликована: Март 15, 2024

Язык: Английский

Процитировано

3

A retrospective chart review of management strategies for lichenoid eruptions associated with immune-checkpoint inhibitor therapy from a single institution DOI Creative Commons

Wylie Masterson,

Alexandria M. Brown, May Ameri

и другие.

Cancer Treatment and Research Communications, Год журнала: 2022, Номер 30, С. 100506 - 100506

Опубликована: Янв. 1, 2022

Immune checkpoint inhibitors and their associated immune-related cutaneous adverse events are continuing to become a mainstay of cancer treatment regimens. While most rashes mild easily manageable, severe or persistent like lichenoid dermatoses can significantly impact the quality life may require ICI cessation. Lichenoid currently have no management guidelines beyond use topical oral steroids. Our study is single-institution retrospective chart review characterize ICI-induced eruptions, treatments, tumor response. We utilized natural language processing our institutional medical record identify patients with eruptions on therapy. One-hundred nineteen were identified, which 108 characterized as dermatitis fifteen mucositis. Most presented diffuse distribution (86%, 101/117), pruritus in (82%, 89/108) pain mucositis (80%, 12/15). Successful treatments for included steroids (81%, 88/108), antihistamines (21%, 23/108), (15%, 16/108). Of patients, 21% (23/108) did not respond (7) required (16). Approximately 28% who had delay, reduction, discontinuation because irCAE. This descriptive highlights patients' ability remain therapy need more effective non-steroidal strategies.

Язык: Английский

Процитировано

5

Delayed Onset of Bullous Pemphigoid Secondary to Nivolumab DOI Open Access
Eric Olsen, Steven A. Svoboda, Sami K. Saikaly

и другие.

Cureus, Год журнала: 2023, Номер unknown

Опубликована: Авг. 9, 2023

The increasing use of immune checkpoint inhibitors, such as nivolumab, a programmed cell death protein 1 (PD-1) inhibitor, for advanced neoplastic disease has revealed significant cutaneous immune-related adverse effects. Herein, we report case bullous pemphigoid (BP) secondary to nivolumab therapy recurrent metastatic oropharyngeal squamous carcinoma. In this patient, the time development BP was three years, which represents most delayed onset PD-1 inhibitor that been reported in literature. Symptoms were initially controlled on low-dose oral prednisone but recurred after two years. patient subsequently treated with several-month taper high-dose prednisone, during he able resume without recurrence skin lesions. Although inhibitor-induced remains rare, physicians should be aware serious event drug class continues expand.

Язык: Английский

Процитировано

2

Cutaneous adverse events due to checkpoint inhibitors – a retrospective analysis at a tertiary referral hospital in Switzerland 2019-2022 DOI Creative Commons

Clara Furrer-Matcau,

Chloé Sieber, Dirk Lehnick

и другие.

Frontiers in Oncology, Год журнала: 2024, Номер 14

Опубликована: Дек. 5, 2024

Checkpoint inhibitors are increasingly important in anti-cancer treatment. Therefore, knowledge of immune-related cutaneous adverse events (ir-cAE) is crucial for therapy management and continuation.

Язык: Английский

Процитировано

0

Cutaneous Immune-Related Adverse Events Secondary to Immune Checkpoint Inhibitors and Their Management DOI

John M. Pach,

Jonathan S. Leventhal

Critical Reviews in Immunology, Год журнала: 2022, Номер 42(4), С. 1 - 20

Опубликована: Янв. 1, 2022

Immune checkpoint inhibitors (CPIs) are highly effective in the treatment of various cancers. Immunotherapy enhances antitumor activity by relieving inhibition T cells responsible for immune surveillance. However, overactivation leads to immune-related adverse events (irAE), which cutaneous most common. Examples include pruritus and maculopapular eruption commonly, psoriasis bullous dermatoses less and, rarely, severe, life-threatening eruptions such as Stevens-Johnson Syndrome or Toxic Epidermal Necrolysis. Many these autoimmune nature, may present <i>de novo</i> recurrence pre-existing disease. In order maximize therapeutic potential CPIs, it is essential recognize effectively manage irAE, can otherwise lead interruption discontinuation. This review summarizes presentation management dermatologic secondary dysregulation a result inhibitor therapy, including common (maculopapular eruption, pruritus, lichenoid dermatitis, vitiligo), (psoriasis, pemphigoid, erythema multiforme, eczematous alopecia areata, granulo-matous neutrophilic dermatoses), severe (acute generalized exanthematous pustulosis &#91;AGEP&#93;, drug reaction with eosinophilia systemic symptoms &#91;DRESS&#93;, syndrome toxic epidermal necrolysis &#91;SJS/TEN&#93;), well exacerbation disease (subacute lupus erythematosus, dermatomyositis, eosinophilic fasciitis, leukocytoclastic vasculitis, scleroderma-like reaction).

Язык: Английский

Процитировано

2