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Article Dans Une Revue European Journal of Cancer Année : 2022

Diagnosis and treatment of Merkel cell carcinoma: European consensus-based interdisciplinary guideline – Update 2022

1 HIPI (UMR_S_976 / U976) - Immunologie humaine, physiopathologie & immunothérapie
2 AP-HP - Hopital Saint-Louis [AP-HP]
3 UNIPG - Università degli Studi di Perugia = University of Perugia
4 DKTK - German Cancer Consortium [Heidelberg]
5 BECCOH - Biomarqueurs et essais cliniques en Cancérologie et Onco-Hématologie
6 Hôpital Ambroise Paré [AP-HP]
7 MV2C - Mount Vernon Cancer Centre [Northwood, UK]
8 Nantes Univ - Nantes Université
9 CIC Nantes - Centre d’Investigation Clinique de Nantes
10 CRCINA - Centre de Recherche en Cancérologie et Immunologie Nantes-Angers
11 ULB - Université libre de Bruxelles
12 University Emergency Hospital [Bucharest]
13 UNIVAQ - University of L'Aquila [Italy]
14 AMU - Aix Marseille Université
15 APHM - Assistance Publique - Hôpitaux de Marseille
16 University of Manchester [Manchester]
17 University Hospital Schleswig-Holstein [Kiel, Germany]
18 Medizinische Universität Wien = Medical University of Vienna
19 QMUL - Queen Mary University of London
20 Maastricht University [Maastricht]
21 Frankfurt University Hospital
22 Aristotle University of Thessaloniki
23 University of Barcelona
24 Hospital Universitario Virgen Macarena [Séville]
25 Unicatt - Università cattolica del Sacro Cuore = Catholic University of the Sacred Heart [Roma]
26 UNIMORE - Università degli Studi di Modena e Reggio Emilia = University of Modena and Reggio Emilia
27 NKUA - National and Kapodistrian University of Athens
28 CHUC - Coimbra Hospital and Universitary Centre [Coimbra, Portugal]
29 Università degli studi di Trieste = University of Trieste
30 Antoni van Leeuwenhoek Hospital
31 Eberhard Karls Universität Tübingen = Eberhard Karls University of Tuebingen
Jurgen C Becker
Ana M Forsea
Maria Concetta Fargnoli
Aimilios Lallas

Résumé

Merkel cell carcinoma (MCC) is a rare skin cancer, accounting for less than 1% of all cutaneous malignancies. It is found predominantly in white populations and risk factors include advanced age, ultraviolet exposure, male sex, immunosuppression, such as AIDS/HIV infection, haematological malignancies or solid organ transplantation, and Merkel cell polyomavirus infection. MCC is an aggressive tumour with 26% of cases presenting lymph node involvement at diagnosis and 8% with distant metastases. Five-year overall survival rates range between 48% and 63%. Two subsets of MCC have been characterised with distinct molecular pathogenetic pathways: ultraviolet-induced MCC versus virus-positive MCC, which carries a better prognosis. In both subtypes, there are alterations in the retinoblastoma protein and p53 gene structure and function. MCC typically manifests as a red nodule or plaque with fast growth, most commonly on sun exposed areas. Histopathology (small-cell neuroendocrine appearance) and immunohistochemistry (CK20 positivity and TTF-1 negativity) confirm the diagnosis. The current staging systems are the American Joint Committee on Cancer/Union for international Cancer control 8th edition. Baseline whole body imaging is encouraged to rule out regional and distant metastasis. For localised MCC, first-line treatment is surgical excision with postoperative margin assessment followed by adjuvant radiation therapy (RT). Sentinel lymph node biopsy is recommended in all patients with MCC without clinically detectable lymph nodes or distant metastasis. Adjuvant RT alone, eventually combined with complete lymph nodes dissection is proposed in case of micrometastatic nodal involvement. In case of macroscopic nodal involvement, the standard of care is complete lymph nodes dissection potentially followed by post-operative RT. Immunotherapy with anti-PD-(L)1 antibodies should be offered as first-line systemic treatment in advanced MCC. Chemotherapy can be used when patients fail to respond or are intolerant for anti-PD-(L)1 immunotherapy or clinical trials.

Domaines

Cancer
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Dates et versions

hal-03775799 , version 1 (06-06-2023)

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Paternité - Pas d'utilisation commerciale - Pas de modification

Identifiants

Citer

Marie-Léa Gauci, Cynthia Aristei, Jurgen C Becker, Astrid Blom, Véronique Bataille, et al.. Diagnosis and treatment of Merkel cell carcinoma: European consensus-based interdisciplinary guideline – Update 2022. European Journal of Cancer, 2022, 171, pp.203-231. ⟨10.1016/j.ejca.2022.03.043⟩. ⟨hal-03775799⟩
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