TY - JOUR
T1 - The Multidisciplinary Management of Cutaneous Squamous Cell Carcinoma
T2 - A Comprehensive Review and Clinical Recommendations by a Panel of Experts
AU - Stanganelli, Ignazio
AU - Spagnolo, Francesco
AU - Argenziano, Giuseppe
AU - Ascierto, Paolo A
AU - Bassetto, Franco
AU - Bossi, Paolo
AU - Donato, Vittorio
AU - Massi, Daniela
AU - Massone, Cesare
AU - Patuzzo, Roberto
AU - Pellacani, Giovanni
AU - Quaglino, Pietro
AU - Queirolo, Paola
AU - Zalaudek, Iris
AU - Palmieri, Giuseppe
AU - On Behalf Of Italian Melanoma Intergroup Imi, null
PY - 2022/1/13
Y1 - 2022/1/13
N2 - Cutaneous squamous cell carcinomas (CSCC) account for about 20% of all keratinocyte carcinomas, which are the most common form of cancer. Heterogeneity of treatments and low mortality are a challenge in obtaining accurate incidence data and consistent registration in cancer registries. Indeed, CSCC mostly presents as an indolent, low-risk lesion, with five-year cure rates greater than 90% after surgical excision, and only few tumors are associated with a high-risk of local or distant relapse; therefore, it is particularly relevant to identify high-risk lesions among all other low-risk CSCCs for the proper diagnostic and therapeutic management. Chemotherapy achieves mostly short-lived responses that do not lead to a curative effect and are associated with severe toxicities. Due to an etiopathogenesis largely relying on chronic UV radiation exposure, CSCC is among the tumors with the highest rate of somatic mutations, which are associated with increased response rates to immunotherapy. Thanks to such strong pre-clinical rationale, clinical trials led to the approval of anti-PD-1 cemiplimab by the FDA (Food and Drug Administration) and EMA (European Medicines Agency), and anti-PD-1 pembrolizumab by the FDA only. Here, we provide a literature review and clinical recommendations by a panel of experts regarding the diagnosis, treatment, and follow-up of CSCC.
AB - Cutaneous squamous cell carcinomas (CSCC) account for about 20% of all keratinocyte carcinomas, which are the most common form of cancer. Heterogeneity of treatments and low mortality are a challenge in obtaining accurate incidence data and consistent registration in cancer registries. Indeed, CSCC mostly presents as an indolent, low-risk lesion, with five-year cure rates greater than 90% after surgical excision, and only few tumors are associated with a high-risk of local or distant relapse; therefore, it is particularly relevant to identify high-risk lesions among all other low-risk CSCCs for the proper diagnostic and therapeutic management. Chemotherapy achieves mostly short-lived responses that do not lead to a curative effect and are associated with severe toxicities. Due to an etiopathogenesis largely relying on chronic UV radiation exposure, CSCC is among the tumors with the highest rate of somatic mutations, which are associated with increased response rates to immunotherapy. Thanks to such strong pre-clinical rationale, clinical trials led to the approval of anti-PD-1 cemiplimab by the FDA (Food and Drug Administration) and EMA (European Medicines Agency), and anti-PD-1 pembrolizumab by the FDA only. Here, we provide a literature review and clinical recommendations by a panel of experts regarding the diagnosis, treatment, and follow-up of CSCC.
U2 - 10.3390/cancers14020377
DO - 10.3390/cancers14020377
M3 - Review article
C2 - 35053539
SN - 2072-6694
VL - 14
JO - Cancers
JF - Cancers
IS - 2
ER -