Checkpoint immunotherapy of cutaneous squamous cell carcinoma in patients suffering from chronic lymphocytic leukaemia: divergent outcomes in two men treated with PD-1 inhibitors.


Journal

Journal of the European Academy of Dermatology and Venereology : JEADV
ISSN: 1468-3083
Titre abrégé: J Eur Acad Dermatol Venereol
Pays: England
ID NLM: 9216037

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 14 02 2021
accepted: 21 04 2021
entrez: 2 12 2021
pubmed: 3 12 2021
medline: 15 12 2021
Statut: ppublish

Résumé

Cutaneous squamous cell carcinoma (cSCC) numbers among the most common types of skin cancer and is known as one of the cancer entities with the highest mutational burden among all solid tumours. Due to the positive correlation between mutational burden and response rate to inhibitors of the programmed cell death 1 (PD-1), those inhibitors are considered promising candidates for the systemic therapy of cSCC. Recently, the PD-1 inhibitors pembrolizumab, nivolumab and cemiplimab demonstrated efficacy in the systemic treatment of locally advanced or metastatic cSCC leading to the approval of cemiplimab by the FDA (U.S. Food and Drug Administration) in 2018 and the EMA (European Medicines Agency) in 2019. Patients with haematological malignancies tend to develop skin cancers of high aggressiveness, enhanced cumulative recurrence rate and higher rates of metastases with subsequent death. Chronic lymphocytic leukaemia (CLL) is the most frequent type of leukaemia in the United States and Europe with the majority of patients older than 50 years of age. This neoplasm predominantly originates from B -cells leading to an impaired immune system of the patient. Although CLL is a B-cell malignancy, studies have also described the involvement of T cells in the pathogenesis and progression of the disease with contradictory findings on the effects of PD-1 inhibitors in CLL. Due to their underlying hematologic malignancy, these patients have commonly no access to PD-1 inhibitor trials for treatment of advanced cSCC. We report on two patients with locally advanced or metastatic cSCC. Both patients had been suffering from a CLL for many years without indication for treatment. Despite a potential immunosuppressive state of the patients due to their CLL, both were treated with the PD-1 inhibitor pembrolizumab resulting in different therapy outcomes.

Identifiants

pubmed: 34855243
doi: 10.1111/jdv.17405
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-44

Subventions

Organisme : Sanofi

Informations de copyright

© 2021 European Academy of Dermatology and Venereology.

Références

Hallek M. Chronic lymphocytic leukemia: 2020 update on diagnosis, risk stratification and treatment. Am J Hematol 2019; 94: 1266-1287.
Griggio V, Perutelli F, Salvetti C et al. Immune dysfunctions and immune-based therapeutic interventions in chronic lymphocytic leukemia. Front Immunol 2020; 11: 594556.
Collins L, Quinn A, Stasko T. Skin Cancer and Immunosuppression. Dermatol Clin 2019; 37: 83-94.
Christopoulos P, Pfeifer D, Bartholome K et al. Definition and characterization of the systemic T-cell dysregulation in untreated indolent B-cell lymphoma and very early CLL. Blood 2011; 117: 3836-3846.
Kipps TJ, Stevenson FK, Wu CJ et al. Chronic lymphocytic leukaemia. Nat Rev Dis Primers 2017; 3: 17008.
Migden MR, Rischin D, Schmults CD et al. PD-1 blockade with cemiplimab in advanced cutaneous squamous-cell carcinoma. N Engl J Med 2018; 379: 341-351.
Leiter U, Loquai C, Reinhardt L et al. Immune checkpoint inhibition therapy for advanced skin cancer in patients with concomitant hematological malignancy: a retrospective multicenter DeCOG study of 84 patients. J Immunother Cancer 2020; 8: e000897.

Auteurs

P Jansen (P)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

G C Lodde (GC)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

A Wetter (A)

Department of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

A Welt (A)

Department of Medical Oncology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

M Stuschke (M)

Department of Radiotherapy, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

U Dührsen (U)

Department of Hematology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

I Stoffels (I)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

J Klode (J)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

E Livingstone (E)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

L Zimmer (L)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

A Roesch (A)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

E Hadaschik (E)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

K G Griewank (KG)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Dermatopathologie bei Mainz, Nieder-Olm, Germany.

D Schadendorf (D)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

S Ugurel (S)

Department of Dermatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

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Classifications MeSH