Diagnosis and treatment of basal cell carcinoma: European consensus–based interdisciplinary guidelines

Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organization of Research and Treatment of Cancer collaborated to develop recommendations o...

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Veröffentlicht in:European journal of cancer (1990) Jg. 118; S. 10 - 34
Hauptverfasser: Peris, Ketty, Fargnoli, Maria Concetta, Garbe, Claus, Kaufmann, Roland, Bastholt, Lars, Seguin, Nicole Basset, Bataille, Veronique, Marmol, Veronique del, Dummer, Reinhard, Harwood, Catherine A., Hauschild, Axel, Höller, Christoph, Haedersdal, Merete, Malvehy, Josep, Middleton, Mark R., Morton, Colin A., Nagore, Eduardo, Stratigos, Alexander J., Szeimies, Rolf-Markus, Tagliaferri, Luca, Trakatelli, Myrto, Zalaudek, Iris, Eggermont, Alexander, Grob, Jean Jacques
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England Elsevier Ltd 01.09.2019
Elsevier Science Ltd
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ISSN:0959-8049, 1879-0852, 1879-0852
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Abstract Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organization of Research and Treatment of Cancer collaborated to develop recommendations on diagnosis and treatment of BCC. A new classification into ‘easy-to-treat (common) BCC and ‘difficult-to-treat’ BCC is proposed. Diagnosis is based on clinicodermatoscopic features for ‘easy-to-treat’ BCCs. Histopathological confirmation is mandatory in ambiguous lesions and in BCCs located in high-risk areas. The first-line treatment of ‘easy-to-treat’ BCC is complete surgery. Microscopically controlled surgery shall be offered for high-risk BCC, recurrent BCC and BCC in critical anatomical sites. Topical therapies (5% imiquimod, 5% fluorouracil) and destructive approaches (curettage, electrocautery, cryotherapy, laser ablation) should be considered in patients with low-risk superficial BCC. Photodynamic therapy is an effective treatment for superficial BCC and thin nodular BCC. The therapy for a ‘difficult-to-treat’ BCC should preferentially be discussed by a multidisciplinary tumour board. Hedgehog inhibitors, vismodegib or sonidegib, should be offered to patients with locally advanced and metastatic BCCs. Immunotherapy with anti–programmed cell death 1 (PD-1) antibodies is a promising therapeutic option, currently being investigated in clinical trials. Radiotherapy represents a valid alternative to surgery for BCC on the face, especially in elderly patients. In patients with naevoid basal cell carcinoma syndrome (NBCCS), close surveillance and regular skin examinations are required to diagnose and treat BCCs at early stage. Long-term follow-up is recommended in patients with high-risk BCC subtypes, high-risk sites, multiple BCCs and NBCCS. •Basal cell carcinoma (BCC) is the most common epithelial malignant tumour in white populations.•A new classification into “easy-to-treat” (common) BCC and “difficult-to-treat” BCC is proposed.•Surgery is the first-line therapy in all types of BCCs.•Treatment choice for advanced BCC should be discussed by a multidisciplinary tumour board.•Hedgehog inhibitors are used in "difficult-to-treat" BCC, and immunotherapy is a promising treatment under investigation.
AbstractList Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organization of Research and Treatment of Cancer collaborated to develop recommendations on diagnosis and treatment of BCC. A new classification into 'easy-to-treat (common) BCC and 'difficult-to-treat' BCC is proposed. Diagnosis is based on clinicodermatoscopic features for 'easy-to-treat' BCCs. Histopathological confirmation is mandatory in ambiguous lesions and in BCCs located in high-risk areas. The first-line treatment of 'easy-to-treat' BCC is complete surgery. Microscopically controlled surgery shall be offered for high-risk BCC, recurrent BCC and BCC in critical anatomical sites. Topical therapies (5% imiquimod, 5% fluorouracil) and destructive approaches (curettage, electrocautery, cryotherapy, laser ablation) should be considered in patients with low-risk superficial BCC. Photodynamic therapy is an effective treatment for superficial BCC and thin nodular BCC. The therapy for a 'difficult-to-treat' BCC should preferentially be discussed by a multidisciplinary tumour board. Hedgehog inhibitors, vismodegib or sonidegib, should be offered to patients with locally advanced and metastatic BCCs. Immunotherapy with anti-programmed cell death 1 (PD-1) antibodies is a promising therapeutic option, currently being investigated in clinical trials. Radiotherapy represents a valid alternative to surgery for BCC on the face, especially in elderly patients. In patients with naevoid basal cell carcinoma syndrome (NBCCS), close surveillance and regular skin examinations are required to diagnose and treat BCCs at early stage. Long-term follow-up is recommended in patients with high-risk BCC subtypes, high-risk sites, multiple BCCs and NBCCS.
Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organization of Research and Treatment of Cancer collaborated to develop recommendations on diagnosis and treatment of BCC. A new classification into 'easy-to-treat (common) BCC and 'difficult-to-treat' BCC is proposed. Diagnosis is based on clinicodermatoscopic features for 'easy-to-treat' BCCs. Histopathological confirmation is mandatory in ambiguous lesions and in BCCs located in high-risk areas. The first-line treatment of 'easy-to-treat' BCC is complete surgery. Microscopically controlled surgery shall be offered for high-risk BCC, recurrent BCC and BCC in critical anatomical sites. Topical therapies (5% imiquimod, 5% fluorouracil) and destructive approaches (curettage, electrocautery, cryotherapy, laser ablation) should be considered in patients with low-risk superficial BCC. Photodynamic therapy is an effective treatment for superficial BCC and thin nodular BCC. The therapy for a 'difficult-to-treat' BCC should preferentially be discussed by a multidisciplinary tumour board. Hedgehog inhibitors, vismodegib or sonidegib, should be offered to patients with locally advanced and metastatic BCCs. Immunotherapy with anti-programmed cell death 1 (PD-1) antibodies is a promising therapeutic option, currently being investigated in clinical trials. Radiotherapy represents a valid alternative to surgery for BCC on the face, especially in elderly patients. In patients with naevoid basal cell carcinoma syndrome (NBCCS), close surveillance and regular skin examinations are required to diagnose and treat BCCs at early stage. Long-term follow-up is recommended in patients with high-risk BCC subtypes, high-risk sites, multiple BCCs and NBCCS.Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organization of Research and Treatment of Cancer collaborated to develop recommendations on diagnosis and treatment of BCC. A new classification into 'easy-to-treat (common) BCC and 'difficult-to-treat' BCC is proposed. Diagnosis is based on clinicodermatoscopic features for 'easy-to-treat' BCCs. Histopathological confirmation is mandatory in ambiguous lesions and in BCCs located in high-risk areas. The first-line treatment of 'easy-to-treat' BCC is complete surgery. Microscopically controlled surgery shall be offered for high-risk BCC, recurrent BCC and BCC in critical anatomical sites. Topical therapies (5% imiquimod, 5% fluorouracil) and destructive approaches (curettage, electrocautery, cryotherapy, laser ablation) should be considered in patients with low-risk superficial BCC. Photodynamic therapy is an effective treatment for superficial BCC and thin nodular BCC. The therapy for a 'difficult-to-treat' BCC should preferentially be discussed by a multidisciplinary tumour board. Hedgehog inhibitors, vismodegib or sonidegib, should be offered to patients with locally advanced and metastatic BCCs. Immunotherapy with anti-programmed cell death 1 (PD-1) antibodies is a promising therapeutic option, currently being investigated in clinical trials. Radiotherapy represents a valid alternative to surgery for BCC on the face, especially in elderly patients. In patients with naevoid basal cell carcinoma syndrome (NBCCS), close surveillance and regular skin examinations are required to diagnose and treat BCCs at early stage. Long-term follow-up is recommended in patients with high-risk BCC subtypes, high-risk sites, multiple BCCs and NBCCS.
Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organization of Research and Treatment of Cancer collaborated to develop recommendations on diagnosis and treatment of BCC. A new classification into ‘easy-to-treat (common) BCC and ‘difficult-to-treat’ BCC is proposed. Diagnosis is based on clinicodermatoscopic features for ‘easy-to-treat’ BCCs. Histopathological confirmation is mandatory in ambiguous lesions and in BCCs located in high-risk areas. The first-line treatment of ‘easy-to-treat’ BCC is complete surgery. Microscopically controlled surgery shall be offered for high-risk BCC, recurrent BCC and BCC in critical anatomical sites. Topical therapies (5% imiquimod, 5% fluorouracil) and destructive approaches (curettage, electrocautery, cryotherapy, laser ablation) should be considered in patients with low-risk superficial BCC. Photodynamic therapy is an effective treatment for superficial BCC and thin nodular BCC. The therapy for a ‘difficult-to-treat’ BCC should preferentially be discussed by a multidisciplinary tumour board. Hedgehog inhibitors, vismodegib or sonidegib, should be offered to patients with locally advanced and metastatic BCCs. Immunotherapy with anti–programmed cell death 1 (PD-1) antibodies is a promising therapeutic option, currently being investigated in clinical trials. Radiotherapy represents a valid alternative to surgery for BCC on the face, especially in elderly patients. In patients with naevoid basal cell carcinoma syndrome (NBCCS), close surveillance and regular skin examinations are required to diagnose and treat BCCs at early stage. Long-term follow-up is recommended in patients with high-risk BCC subtypes, high-risk sites, multiple BCCs and NBCCS. •Basal cell carcinoma (BCC) is the most common epithelial malignant tumour in white populations.•A new classification into “easy-to-treat” (common) BCC and “difficult-to-treat” BCC is proposed.•Surgery is the first-line therapy in all types of BCCs.•Treatment choice for advanced BCC should be discussed by a multidisciplinary tumour board.•Hedgehog inhibitors are used in "difficult-to-treat" BCC, and immunotherapy is a promising treatment under investigation.
Author Bataille, Veronique
Middleton, Mark R.
Marmol, Veronique del
Stratigos, Alexander J.
Eggermont, Alexander
Höller, Christoph
Harwood, Catherine A.
Bastholt, Lars
Zalaudek, Iris
Haedersdal, Merete
Szeimies, Rolf-Markus
Peris, Ketty
Malvehy, Josep
Dummer, Reinhard
Trakatelli, Myrto
Tagliaferri, Luca
Grob, Jean Jacques
Fargnoli, Maria Concetta
Morton, Colin A.
Seguin, Nicole Basset
Hauschild, Axel
Garbe, Claus
Nagore, Eduardo
Kaufmann, Roland
Author_xml – sequence: 1
  givenname: Ketty
  surname: Peris
  fullname: Peris, Ketty
  email: ketty.peris@unicatt.it
  organization: Institute of Dermatology, Catholic University of the Sacred Heart, Italy
– sequence: 2
  givenname: Maria Concetta
  surname: Fargnoli
  fullname: Fargnoli, Maria Concetta
  organization: Department of Dermatology, University of L'Aquila, L'Aquila, Italy
– sequence: 3
  givenname: Claus
  surname: Garbe
  fullname: Garbe, Claus
  organization: Centre for Dermatooncology, Department of Dermatology, Eberhard-Karls University, Tuebingen, Germany
– sequence: 4
  givenname: Roland
  surname: Kaufmann
  fullname: Kaufmann, Roland
  organization: Department of Dermatology, Venereology and Allergology, University Hospital Frankfurt, Germany
– sequence: 5
  givenname: Lars
  orcidid: 0000-0001-5478-9826
  surname: Bastholt
  fullname: Bastholt, Lars
  organization: Department of Oncology, Odense University Hospital, Denmark
– sequence: 6
  givenname: Nicole Basset
  surname: Seguin
  fullname: Seguin, Nicole Basset
  organization: Dermatology Department, Saint-Louis Hospital, Paris, France
– sequence: 7
  givenname: Veronique
  surname: Bataille
  fullname: Bataille, Veronique
  organization: Twin Research and Genetic Epidemiology Unit, School of Basic & Medical Biosciences, King's College London, London, SE1 7EH, UK
– sequence: 8
  givenname: Veronique del
  surname: Marmol
  fullname: Marmol, Veronique del
  organization: Department of Dermatology, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium
– sequence: 9
  givenname: Reinhard
  surname: Dummer
  fullname: Dummer, Reinhard
  organization: Department of Dermatology, University Hospital Zurich and University Zurich, Switzerland
– sequence: 10
  givenname: Catherine A.
  surname: Harwood
  fullname: Harwood, Catherine A.
  organization: Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom
– sequence: 11
  givenname: Axel
  surname: Hauschild
  fullname: Hauschild, Axel
  organization: Department of Dermatology, University of Kiel, Kiel, Germany
– sequence: 12
  givenname: Christoph
  surname: Höller
  fullname: Höller, Christoph
  organization: Department of Dermatology, Medical University of Vienna, Austria
– sequence: 13
  givenname: Merete
  surname: Haedersdal
  fullname: Haedersdal, Merete
  organization: Department of Dermatology, University of Copenhagen, Bispebjerg Hospital, Copenhagen, Denmark
– sequence: 14
  givenname: Josep
  surname: Malvehy
  fullname: Malvehy, Josep
  organization: Department of Dermatology, Hospital Clínic de Barcelona (Melanoma Unit), University of Barcelona, IDIBAPS, Barcelona & CIBERER, Barcelona, Spain
– sequence: 15
  givenname: Mark R.
  orcidid: 0000-0003-0167-1685
  surname: Middleton
  fullname: Middleton, Mark R.
  organization: Department of Oncology, University of Oxford, Old Road Campus, Oxford, OX3 9DU, UK
– sequence: 16
  givenname: Colin A.
  surname: Morton
  fullname: Morton, Colin A.
  organization: Stirling Community Hospital, Stirling, UK
– sequence: 17
  givenname: Eduardo
  orcidid: 0000-0003-3433-8707
  surname: Nagore
  fullname: Nagore, Eduardo
  organization: Department of Dermatology, Instituto Valenciano de Oncologia, Valencia, Spain
– sequence: 18
  givenname: Alexander J.
  surname: Stratigos
  fullname: Stratigos, Alexander J.
  organization: 1st Department of Dermatology- Venereology, National and Kapodistrian University of Athens, School of Medicine, Andreas Sygros Hospital, Athens, Greece
– sequence: 19
  givenname: Rolf-Markus
  surname: Szeimies
  fullname: Szeimies, Rolf-Markus
  organization: Clinic for Dermatology and Allergology, Klinikum Vest GmbH Teaching Hospital, Recklinghausen, Germany
– sequence: 20
  givenname: Luca
  surname: Tagliaferri
  fullname: Tagliaferri, Luca
  organization: Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC di Radioterapia, Dipartimento di Scienze Radiologiche, Radioterapiche Ed Ematologiche, Rome, Italy
– sequence: 21
  givenname: Myrto
  surname: Trakatelli
  fullname: Trakatelli, Myrto
  organization: Second Department of Dermatology, Aristotle University Medical School, Papageorgiou General Hospital, Thessaloniki, Greece
– sequence: 22
  givenname: Iris
  orcidid: 0000-0002-7878-4955
  surname: Zalaudek
  fullname: Zalaudek, Iris
  organization: Dermatology Clinic, University of Trieste, Trieste, Italy
– sequence: 23
  givenname: Alexander
  surname: Eggermont
  fullname: Eggermont, Alexander
  organization: Cancer Institute, Gustave Roussy Cancer Campus, Grand Paris, 94805, Villejuif, France
– sequence: 24
  givenname: Jean Jacques
  orcidid: 0000-0002-1014-4062
  surname: Grob
  fullname: Grob, Jean Jacques
  organization: University Department of Dermatology, Marseille, France
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31288208$$D View this record in MEDLINE/PubMed
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Basal cell carcinoma
Photodynamic therapy
Surgical therapy
Immunotherapy
Classification
Hedgehog inhibitors
Destructive therapy
Radiotherapy
Guidelines
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PublicationPlace England
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PublicationTitle European journal of cancer (1990)
PublicationTitleAlternate Eur J Cancer
PublicationYear 2019
Publisher Elsevier Ltd
Elsevier Science Ltd
Publisher_xml – name: Elsevier Ltd
– name: Elsevier Science Ltd
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Snippet Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. Multidisciplinary experts from the European Dermatology Forum, the...
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SubjectTerms 5-Fluorouracil
Antibodies
Apoptosis
Basal cell carcinoma
Cancer
Carcinoma, Basal Cell - mortality
Carcinoma, Basal Cell - pathology
Carcinoma, Basal Cell - therapy
Cell death
Classification
Clinical Decision-Making
Clinical trials
Consensus
Cryotherapy
Curettage
Dermatology
Destructive therapy
Diagnosis
Europe
Geriatrics
Guidelines
Hedgehog inhibitors
Humans
Imiquimod
Immunotherapy
Laser ablation
Medical diagnosis
Medical Oncology - standards
Metastases
Oncology
Patient Selection
Patients
PD-1 protein
Photodynamic therapy
Predictive Value of Tests
Prognosis
Radiation therapy
Radiotherapy
Risk
Risk Assessment
Risk Factors
Skin
Skin cancer
Skin Neoplasms - mortality
Skin Neoplasms - pathology
Skin Neoplasms - therapy
Surgery
Surgical therapy
Topical therapy
Tumors
Title Diagnosis and treatment of basal cell carcinoma: European consensus–based interdisciplinary guidelines
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https://dx.doi.org/10.1016/j.ejca.2019.06.003
https://www.ncbi.nlm.nih.gov/pubmed/31288208
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